SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs539378175 | snp | A/C/T | 0.00398763 | 0.0445073 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458642 | GTGTGTTCATGTCCG[A/C/T]GGCAGCTGTCTTTTT | 899 |
rs539413178 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457386 | GCTGACAGCTTTCAC[A/G]CTTAAGGCACGTGTG | 899 |
rs539584114 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459280 | GCTCTGTTTTTCTTT[C/G]AGCTACCGCCTGGGA | 899 |
rs539622960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454401 | ATCACGAGGAAAGTC[C/T]ATGCAGATACGCACG | 899 |
rs539813804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450163 | AGTGAGTTGATATCA[C/T]GTCACTGGACTCCAG | 899 |
rs539822894 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457898 | AAAAAGAATTTTCCC[A/G]GATAGGCTAGCCAGA | 899 |
rs539844413 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452841 | TCGCGGTAACGTTTG[A/C]TGGGTTTGTCCATGT | 899 |
rs540014252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448395 | CACTTTCTGACCTCC[C/G]CTTTGTTATTATTAT | 899 |
rs540062861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2443286 | TGAAGCTGTGATGAG[A/G]CAGGTGCTCCTATTC | 899 |
rs540075100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2433742 | AGGCACGCGCTACCA[C/T]GCCCATCTAATTTTT | 899 |
rs540241743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445272 | TGGGGCCTGCTTTGG[C/G]GCTGGGACCCACGGA | 899 |
rs540290589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437777 | GGTGGTGCATACCTA[C/T]AGTCCCAGCTACTCA | 899 |
rs540316232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2454637 | GGCTCACGCCCACAC[A/G]CTGGCCTCTAGCCCC | 899 |
rs540359603 | snp | A/G | 0.496034 | 0.0443518 | intron-variant | CCNF | GRCh38.p7 | 16:2449776 | CCCTCCGTCCCCTCC[A/G]TCCCCTCCGTCCCCT | 899 |
rs540374494 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443972 | TCGCCCAGGCTGGAG[G/T]GCAGTGGCGCGATCT | 899 |
rs540385607 | snp | C/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428317 | GTCTGTGTGCCCAGG[C/G]CAGGCCCAGTACTTG | 899 |
rs540411959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2439172 | GCATGATGGTGGGCT[C/T]CTGTAATCCCAGCTA | 899 |
rs540533132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2432482 | GGTCCTGGCCTGGAC[A/G]CTCCTGCGTTGGCCC | 899 |
rs540551199 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454360 | GTGTCACTCCACACA[C/T]GCACCGACTCCCTGG | 899 |
rs540580520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438602 | AGCCGAGATTGCACC[A/G]CTGCACTCCAGCCTG | 899 |
rs540607433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437442 | GGGAAGTGAAGATGC[A/G]GAAAACTGAGAGTGC | 899 |
rs540654596 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2435247 | CAGAGCAGACTCCGT[A/C]TCAAAAAAAAAAAAG | 899 |
rs540691566 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428249 | GTGCTGTGATCACCT[G/T]TTTACTCTGTCTCTT | 899 |
rs540770940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2440869 | TGAGTTGGGAGGATC[A/G]CTTGAGCCCAGGAGT | 899 |
rs540799362 | snp | C/T | 5.11417e-05 | 0.00505651 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456958 | CAGCAACAGGTGAAG[C/T]GGATAAACCTATGCA | 899 |
rs541195656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446286 | GACTGATCAGGGAGG[G/T]TGGCAGTTGGCTGCC | 899 |
rs541219732 | in-del | -/AA | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457798 | AGGTATTAAAAAAAC[-/AA]GAGATTCCCACCATT | 899 |
rs541277119 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429089 | AGCGGCGAAGCCCGA[A/G]CCCATGCGGCCGGGA | 899 |
rs541354125 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2455865 | TGAGGGAGGCAGAGA[A/C]CCTGTCTGGAGTTCA | 899 |
rs541386499 | snp | A/G | 0.00012356 | 0.00785906 | missense | CCNF | GRCh38.p7 | 16:2455564 | GAGAAGGAGGGCGAC[A/G]GTGAGTGTGGGGCCA | 899 |
rs541431976 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2453600 | GTGCCGGCCCAGTTC[C/G]CTCAGCGCTTCCTCA | 899 |
rs541580901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2451756 | TGACCCTCCCTCCCT[C/T]GGGGGCTTCGGCTTC | 899 |
rs541602960 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444154 | TCAATCTCCTGACCT[C/T]GTGATCCGCCCGCTT | 899 |
rs541793691 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2432876 | CAGGAGACCCTACAT[A/C]TGCCTCTCGTCCTCA | 899 |
rs541818713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454058 | ATTCCACAAGGCCCC[A/G]ATGAACAGGGCCCTC | 899 |
rs541978756 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458197 | TGCTGCCATCCACTT[C/T]TGTTTACTCTGCAAA | 899 |
rs542003623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447408 | GCCAACATGGTGAAA[A/C]CCTGTCTCTACTAAA | 899 |
rs542049001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2430157 | AGAGAGGGGAGCCGG[G/T]AGCAATCGCTAGGAA | 899 |
rs542237467 | snp | G/T | 0.317692 | 0.240661 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445726 | TTGGTTTTGTTTTGT[G/T]TTGTTTTTTTTTTTT | 899 |
rs542262385 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CCNF | GRCh38.p7 | 16:2442463 | TATTATATAATATAA[C/T]ATTATTATATATAAT | 899 |
rs542343127 | in-del | -/CAGCCCCACCA | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457344 | GTGTCCTGGTGTTCC[-/CAGCCCCACCA]GAGCCCCGTGCCGGG | 899 |
rs542353558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452933 | TGTGTTTATCCATCC[C/T]GCAGCTGGTGGACAT | 899 |
rs542388461 | snp | C/T | | | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447299 | TTTTTTTTTTAAATC[C/T]GGGGACCAGGCACGG | 899 |
rs542424026 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2436856 | GGGACATGAAGCGTC[G/T]CGGGGTCTCCTTCCC | 899 |
rs542495691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436354 | CATCCCCAGAGGCCA[G/T]GTGCTCCTTGAAAGA | 899 |
rs542589741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2443384 | CTTCCCCAGGCATTA[A/G]CCATGTAAGAAACTG | 899 |
rs542637539 | snp | A/G | | | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456443 | GGGGACCGTAGCAAG[A/G]TAGAAGATTCTTGAC | 899 |
rs542668205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437802 | TACTCAGGAGGCTGC[A/G]GTGGGAGGATCGCTT | 899 |
rs542748372 | snp | C/T | 1.87419e-05 | 0.00306114 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445373 | GCCAGCTTATTTGGT[C/T]GGGCCCAACAGGTGG | 899 |
rs542823527 | in-del | -/ATATATATATATATATATA | 0.00438332 | 0.0466095 | intron-variant | CCNF | GRCh38.p7 | 16:2441951 | ATTATATATATATAT[-/ATATATATATATATATATA]TATATATATATATGT | 899 |
rs542866346 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2434597 | GCCTGAGCAACAGAG[C/T]GAGACTCCGTCTCAA | 899 |
rs542898634 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2433778 | CTTAGTAGAGATGGG[A/G]TTTCGCCATGTTGGC | 899 |
rs542984845 | snp | C/T | 0.00079952 | 0.019978 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444510 | TTTCATCGTATTAGC[C/T]AGGATGGTCTCAATC | 899 |
rs542999594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2432511 | CCAGCGCTTAGGCTC[C/T]GGGTTCTACCTGAGA | 899 |
rs543021686 | snp | A/G | | | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446940 | TGTGTGTGCCAGCTC[A/G]ATGCAGTGTCATTCC | 899 |
rs543044212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2429895 | CCGCAGCCCGGCCGG[G/T]CCCTGACCGAGCCTC | 899 |
rs543066511 | snp | C/T | 1.65162e-05 | 0.00287365 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2435872 | CCTCTACAATGAAGG[C/T]CGTAAGTCCTCACCC | 899 |
rs543215606 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2450204 | AGAGCAAGACTCTGT[C/G]TCTAAAAACAACTGG | 899 |
rs543263972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448142 | CCGGGCACAGACTTT[A/C]CAACAACCCTTGGGC | 899 |
rs543598536 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CCNF | GRCh38.p7 | 16:2437547 | CTGGGTACACGTGCT[A/G]ACAGCTGGAAACATG | 899 |
rs543801813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446845 | GACACCTGTACCTGC[C/T]ACATTCACCTTTGCA | 899 |
rs543813373 | snp | C/T | 7.98594e-05 | 0.00631849 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456551 | TTCCTGCAGTGACAG[C/T]TCCCAGCGGCATCCT | 899 |
rs543847593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2451902 | CCAGAATTCAGGCCA[C/T]ATCTCAACCTTGACC | 899 |
rs543971984 | snp | C/T | 6.5937e-05 | 0.00574144 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443771 | ACAACAAGTCTTCTC[C/T]GTGCAGAAGGGACTC | 899 |
rs543983219 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2441161 | ATTGCTTGAACCCAG[A/G]AGGAGGAAGTTGCAG | 899 |
rs544009612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2441761 | ACCTCAAGTAATCTG[C/T]CCTCCTCGGCCTCCC | 899 |
rs544016617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432579 | GTGACCTGTTTCCAC[A/G]CTCCCACTAGCAAGG | 899 |
rs544042257 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438371 | GCAGATCTCAAGGAG[G/T]CATCGAACCTCGATG | 899 |
rs544089121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2438468 | AAAATGGTGAAACCA[C/T]GTCTTTACTAAAAAA | 899 |
rs544190549 | snp | A/G | 6.78185e-05 | 0.00582277 | intron-variant | CCNF | GRCh38.p7 | 16:2449223 | GCTGGGCCTGCATGC[A/G]GCACTGCACCAAGGA | 899 |
rs544190682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454500 | GGCCCCCCACAGCCC[C/T]ATCAGTCTTCTGAGA | 899 |
rs544238492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2449594 | AGATACAGCACGGCT[C/T]CTACCTTCAGTGATG | 899 |
rs544284173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB, nc-transcript-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458869 | AGATGAGTGATGGAC[A/G]TCCTTCACTGCCTCG | 899 |
rs544370542 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2437877 | GCACTCCAGCCTGGG[G/T]GACAGAGCAAGACCC | 899 |
rs544550720 | snp | C/T | | | missense | CCNF | GRCh38.p7 | 16:2449363 | CACCTGTGCAGCTTC[C/T]TCTGCGAGCTCTCCC | 899 |
rs544567101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450131 | AGAATCGCTTGAACC[C/T]AGGAAGCAGAGGTTG | 899 |
rs544632573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436948 | ACCTGTTCTAGACAT[A/T]AATGAAGTAGGGGGA | 899 |
rs544701042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434831 | CCGGATTTGCCTTTT[C/G]TGAGGATTTCACATG | 899 |
rs544740302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448633 | TGCCCAGGGTGGTCT[C/T]GAACTCCTGGCTGAG | 899 |
rs544754017 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | CCNF | GRCh38.p7 | 16:2446231 | TCTGGCAGGCACAGG[A/C]TGGACTGCCCTGTCC | 899 |
rs544808102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2431667 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA | 899 |
rs544872930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2437380 | GGTCCCAGGACACAG[A/G]AAGACCCCGAGGGTA | 899 |
rs544895557 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433688 | AACTCCTGGTTCAAG[C/T]GATTCTCCTGCCTCA | 899 |
rs544992192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433696 | GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCCTG | 899 |
rs545052921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433178 | CTGTTGCTGTCTCCC[A/G]TGACATTGCCTCATA | 899 |
rs545197468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2451118 | CAGCCCACGTTGGTT[C/T]GTTCCATGCAGTTCA | 899 |
rs545214343 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428159 | TCACCCTCCTTCACC[C/T]GCTTCCTGATTCCGG | 899 |
rs545234686 | snp | C/G | 0.00387116 | 0.0438246 | intron-variant | CCNF | GRCh38.p7 | 16:2449173 | TGCGCTACGCGTGCA[C/G]CATCGGCGTGAACAT | 899 |
rs545287321 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2455138 | AGATGGTTGGCCCAC[A/G]CCCCACAGCTGAGCC | 899 |
rs545393351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2430868 | AGTTTCCCAATAGCC[A/G]AGTTACATGACATGC | 899 |
rs545404064 | snp | C/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444403 | CTCCCGGGTTCACAC[C/T]ATTCTCCTGCCTCAG | 899 |
rs545546727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455757 | GGAGAGCCCCCAAAA[C/G]ACCACAGCTGCTCCC | 899 |
rs545602698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443497 | TAATAATTAAAACCT[A/G]AGCCATCCTTGTTCC | 899 |
rs545673424 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2441344 | AAAGCTGCAGAGAGC[C/T]GTGATCGCAACATTG | 899 |
rs545766358 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454491 | CTTCTCAGAGGCCCC[C/T]CACAGCCCCATCAGT | 899 |
rs545944447 | snp | C/T | 0.000132024 | 0.00812371 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445530 | GTGCCTGCACCTGAC[C/T]GTGGAGTGTGTGGAC | 899 |
rs546066592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2435980 | TGCTGTCCTTGCTCT[A/G]TCCGATGGCCTGCCT | 899 |
rs546071489 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2458062 | CTTTCCTGCTGGCCA[C/T]GGAGACTCTGCTCCT | 899 |
rs546108240 | snp | C/G/T | 0.000283702 | 0.0119069 | intron-variant | CCNF | GRCh38.p7 | 16:2453584 | CAATGCTGGCATCCT[C/G/T]GTGCCGGCCCAGTTC | 899 |
rs546126701 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2432252 | CTGAAATGGACTCTA[A/G]GAGTTATTTTCTAGA | 899 |
rs546285145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437972 | GGAGGGCCAGACAGC[A/G]GGGCCATGGGCATGG | 899 |
rs546365214 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | CCNF | GRCh38.p7 | 16:2442456 | TATATAATATTATAT[A/T]ATATAATATTATTAT | 899 |
rs546545011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437560 | CTGACAGCTGGAAAC[A/G]TGGGGCTGAGGCTGC | 899 |
rs546558454 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2447925 | CCCTGCGCCTCTTGT[C/G]CTCTTGGTCAAGTGA | 899 |
rs546584115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432087 | CGCCCGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 899 |
rs546589213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444565 | TCCGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG | 899 |
rs546624372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432632 | CACATTTCCGTCCTG[A/C]CTGCCCCCTTTTAGA | 899 |
rs546749900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444198 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 899 |
rs546824548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436980 | AAAAGACAGGTGCCC[C/G]CATCCTGGAGGGCTC | 899 |
rs546833027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454201 | GCTGCCTCCAGAAGC[A/G]TTGTGTCGGGAGTGG | 899 |
rs546924374 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2449669 | TTTTTCAAAACTATT[G/T]TAAAAGGATTGCAAC | 899 |
rs546994505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB, nc-transcript-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458934 | CATGGAGTCAGTTCT[C/T]TGCTTTCTCCCAGCT | 899 |
rs547082877 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440718 | CAAATGCTAGGGACA[A/G]AATTACAAATTGATA | 899 |
rs547285284 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2456163 | TAGAATGTTGTTTGA[A/G]GTGTGCCCACGTGGT | 899 |
rs547290055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453763 | AGGCTATTGCCTCTC[A/G]CTCTGACTGGGCTCC | 899 |
rs547353172 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427397 | CCCTCCTCAGTCCTC[A/G]TTTCAGGTGACTGCT | 899 |
rs547393350 | snp | A/C/G | 3.30094e-05 | 0.00406249 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445534 | CTGCACCTGACCGTG[A/C/G]AGTGTGTGGACCGGT | 899 |
rs547581432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446514 | CCCCTAGTTCCGCCT[G/T]TGGAAATAACGTGGA | 899 |
rs547727949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445840 | TCAAGTGATTCTTCT[C/G]CCTCAGCCTCCAGAG | 899 |
rs547751384 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2453548 | AAACGGTTAGTTACC[C/T]TGCGTTCTGGCTGCG | 899 |
rs547786295 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CCNF | GRCh38.p7 | 16:2442808 | TATTCTATAATATAT[A/G]ATATATTCTATAATA | 899 |
rs547863953 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CCNF | GRCh38.p7 | 16:2454782 | AACACCAGAGGGGCC[A/G]GGTGCGGTTGCTCAT | 899 |
rs547891255 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | CCNF | GRCh38.p7 | 16:2434142 | AAAACCCTGTCTCTA[-/T]TAAAAATACAAAAAT | 899 |
rs547961449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2437021 | AAACACAGCTGCTTT[A/G]CACTATGGTGGGCTT | 899 |
rs547978046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452719 | ACTTCCTCAGCGCTA[C/G]ATGACCCCCAGTAGT | 899 |
rs548054377 | in-del | -/T | 0.00127984 | 0.0252643 | intron-variant | CCNF | GRCh38.p7 | 16:2431053 | ATGTAACTTTTATCC[-/T]TTTTTTTTTCCCTTC | 899 |
rs548083797 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454791 | GGGGCCGGGTGCGGT[G/T]GCTCATGCCTGTAAT | 899 |
rs548120156 | snp | A/G | 1.64944e-05 | 0.00287175 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443782 | TCTCCGTGCAGAAGG[A/G]ACTCAATGACACAAT | 899 |
rs548140127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448291 | AAACTGAATGCTCAG[C/G]GCACTTGGGCCTTTT | 899 |
rs548164787 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434835 | ATTTGCCTTTTGTGA[A/G]GATTTCACATGGAAT | 899 |
rs548301773 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457766 | AAGATGAAAACAAAA[A/G]AAAAACTTAAAACAG | 899 |
rs548580990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2435543 | TGAGCTGTGATCGCA[C/G]CACTGCACTCCAGCC | 899 |
rs548620007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436029 | GCTCGTGCCCAGATG[C/T]ACCCTGCTGAGGGAC | 899 |
rs548743331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2441299 | TACTCAGGAGGCTGA[A/G]GCAGGAGGATCACTT | 899 |
rs548818168 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | CCNF | GRCh38.p7 | 16:2429464 | GCGGGCTCCGGCGGC[A/T]GCGACGCGAGCGCGG | 899 |
rs549260639 | snp | C/G | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444279 | TTTGGAAGAAAATAT[C/G]CTACTCTGCTTTCTT | 899 |
rs549283849 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | CCNF | GRCh38.p7 | 16:2449864 | TGTGGGACCTCACCG[C/G]ATTCTCCTATGAAGA | 899 |
rs549314559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444773 | AGCTAATTGTTGTAT[C/T]TTTAGTAGAGACAGG | 899 |
rs549318310 | snp | A/G | 1.66676e-05 | 0.00288679 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456753 | AGGGAAGGACGTCAC[A/G]ACCTCAGGGTACTCC | 899 |
rs549415964 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428451 | AGCCCCCTCTGTCCT[C/T]CACCAGACAGTCAGG | 899 |
rs549471265 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2430474 | CTCACCTTTAATGAT[A/T]GCATCTGTACACAAA | 899 |
rs549479064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2456288 | GTCCTGTCAGTTTCC[C/T]GGTTGCTTGCTTCTG | 899 |
rs549497740 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2441883 | TTCAACCTTACTACT[A/G]GTCATAAGAGTGCAC | 899 |
rs549519557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444210 | AGGCGTGAGCCACCG[C/T]GCCCAGCCTTGGGTG | 899 |
rs549639368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2451553 | AAATCCAGCAGACTC[A/G]GCGGTGTGGGCTTTT | 899 |
rs549684306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2441350 | GCAGAGAGCCGTGAT[C/T]GCAACATTGCACTTC | 899 |
rs549700214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452660 | TTTTCACTTTCCCCA[A/G]AGGGACAACACACCC | 899 |
rs549764947 | snp | A/G | 1.68698e-05 | 0.00290424 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439756 | ATTGACAGGTGTCAG[A/G]TCCTGGGCGATGCCT | 899 |
rs549832018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447064 | AGAGACGACTGAGGA[G/T]GTCGGGCGGCCGCCT | 899 |
rs550100805 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CCNF | GRCh38.p7 | 16:2434352 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 899 |
rs550120647 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427559 | TTCCCTTCTCTCCCC[C/T]GCCCCTCACTACCCA | 899 |
rs550490927 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2440225 | CTTCCTGCTTCCTCT[G/T]CCTGTTAGCGCCTTG | 899 |
rs550848660 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458294 | GTTTTGCTCTTGTCT[C/T]CCCGGCTGGAGTGCA | 899 |
rs550970231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436416 | CTGCTTATCTGCTCA[A/G]CACCCCAAGGAACGA | 899 |
rs550970535 | snp | G/T | 0.000869943 | 0.0208378 | intron-variant | CCNF | GRCh38.p7 | 16:2429548 | ACACCCCTTCTGCCT[G/T]CCCTGCGGGGCGGAC | 899 |
rs551381632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433955 | GGGCTGCTTCCAGGG[G/T]GAATGTATATATTTC | 899 |
rs551402760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455640 | GGCCTCTGGGCACCC[A/G]GCCCTGTGCGAGCGC | 899 |
rs551477560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454376 | GCACCGACTCCCTGG[A/G]GCCAGGGTCATCACG | 899 |
rs551507662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2456025 | AATTAGCTGGGCATC[C/G]TGGCGTGCGCCTGTG | 899 |
rs551566151 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2440841 | CGCCTGCAATCCCAG[A/C]GCTGTAGGAGGTTGA | 899 |
rs551652508 | snp | C/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443435 | AGGCCACTGACATTT[C/T]ATTATATATCTTTTC | 899 |
rs551656222 | snp | C/T | 6.62e-05 | 0.00575288 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445470 | CAGGTACATTCTGAT[C/T]GACTGGCTGGTGGAA | 899 |
rs551683861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2450282 | AAGCGGGCGGATCAC[C/T]GAGGTCAGGAGTTCA | 899 |
rs551692958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438768 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACCTGAG | 899 |
rs551923115 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CCNF | GRCh38.p7 | 16:2442639 | ATATAATATTATATA[A/G]TATAATATTATTATA | 899 |
rs551964900 | snp | G/T | 1.65578e-05 | 0.00287726 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456822 | TGGCTTGGGGGCCCT[G/T]CCCCAACCTACCTCA | 899 |
rs552081999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448228 | TTTCTACCCCACTGA[C/T]AGAGCTGTCACGTGA | 899 |
rs552086108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2442218 | TTCACCATGTTAGCC[A/G]GGATGGTCTGGATCT | 899 |
rs552106857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452680 | ACAACACACCCCTCA[A/G]CTGTCACCCTCCCGT | 899 |
rs552266055 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457244 | TCTTTGGAAAGTTTA[G/T]CCTGGAAGCAGTTGG | 899 |
rs552296156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2435009 | CTTGTAATCCCAGCA[C/G]TTTGGGAGGCCGAGG | 899 |
rs552358591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436443 | ACGAGCCCATGATCT[A/G]TCCCAGCTCTCAAAA | 899 |
rs552501292 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427684 | AGTGGGAAACGGGCC[C/T]ACACCCTGGAGGAGC | 899 |
rs552665734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2431460 | AAGGGGGGTGGATCA[C/T]CTGAGGTCAGGAGTT | 899 |
rs552695121 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2451350 | GACCAGTGGGGCTGG[C/G]GGCCATGAGTGGAGT | 899 |
rs552710005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2430687 | CCAGACTCTTCAAGC[C/T]CACAGATCTTTATTG | 899 |
rs552816940 | snp | C/T | 0.00777916 | 0.0618794 | intron-variant | CCNF | GRCh38.p7 | 16:2449152 | CCACGTCGCCATCTG[C/T]GCTGGTGCGCTACGC | 899 |
rs552825346 | snp | C/T | 0.00010193 | 0.00713825 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437149 | GTGTCTGATGAGGCC[C/T]GCGCAGAAGTGAATG | 899 |
rs552851697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2454403 | CACGAGGAAAGTCCA[C/T]GCAGATACGCACGGC | 899 |
rs553172969 | snp | A/G | 1.65814e-05 | 0.00287931 | synonymous-codon, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456927 | TCCCCCAAGTCCCCC[A/G]GAGAGCAGTGTTCCC | 899 |
rs553253334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453960 | TGGACCTGTTTACCC[A/G]CCTCTCCTATCTCAG | 899 |
rs553385838 | snp | A/G | 1.65364e-05 | 0.0028754 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453472 | CAGCCCCGACCCCCC[A/G]ACTTTCCTCAGCACA | 899 |
rs553393216 | in-del | -/ATG | 0.00874735 | 0.0655527 | intron-variant | CCNF | GRCh38.p7 | 16:2448409 | CCCTTTGTTATTATT[-/ATG]ATGATTATTTTTTGA | 899 |
rs553449267 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2450578 | GAGAGCAGCTGCTCC[C/T]AACCCAAGCTCATTG | 899 |
rs553453842 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457399 | ACGCTTAAGGCACGT[A/G]TGACCTGGGTAGTCA | 899 |
rs553535827 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436766 | GAATATTCTCCTCGT[A/C/G]CCAAAAAGAACCCCC | 899 |
rs553573316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2443345 | CGGAGAGCACTGGGG[C/T]GTATGGCCAGAGACT | 899 |
rs553578806 | in-del | -/A | 0.472616 | 0.113763 | intron-variant | CCNF | GRCh38.p7 | 16:2431680 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 899 |
rs553608689 | snp | A/G | 3.66609e-05 | 0.00428125 | missense | CCNF | GRCh38.p7 | 16:2455435 | GACAGAGGCAGCTTC[A/G]TTACCACCCCCACTG | 899 |
rs553686501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455669 | GCTGTGGGAGGAAGA[C/T]GTGCACAGAGTGCGG | 899 |
rs553697255 | snp | A/G/T | 0.00319098 | 0.0398384 | intron-variant | CCNF | GRCh38.p7 | 16:2448020 | GGGAAGGTGCCTTGC[A/G/T]GGGGGCCGCTGGAGC | 899 |
rs553732066 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CCNF | GRCh38.p7 | 16:2442457 | ATATAATATTATATA[A/G]TATAATATTATTATA | 899 |
rs553734079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448441 | AGACAGTGTCTTGCT[C/T]TGTCACCCAGGTTGG | 899 |
rs553848149 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442755 | TTATATAATAATTAT[A/T]ATAATATAATATATA | 899 |
rs553878089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444466 | CACCACGCCCAGCTA[A/T]TTTTTTTGTATTTTT | 899 |
rs553894078 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2431752 | ATGCTTTCTTTAAGA[C/G]ATTCTGATTACAGAA | 899 |
rs553947581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454889 | TCATGGTGAAACCCC[A/G]TTTCTACTAAAAATA | 899 |
rs554099068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445695 | GTCACCTGCCCTTCA[A/T]GTGCTCCTCACTGGT | 899 |
rs554108597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2435748 | CTTCAAGTGCTGTAG[G/T]AGTTCATAACGTTTG | 899 |
rs554108642 | snp | A/T | 0.151334 | 0.229706 | intron-variant | CCNF | GRCh38.p7 | 16:2442433 | TAATATAATATTATT[A/T]TATATAATATATAAT | 899 |
rs554202140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432625 | CACAAAACACATTTC[C/T]GTCCTGCCTGCCCCC | 899 |
rs554209971 | snp | C/T | 2.62512e-05 | 0.00362283 | intron-variant | CCNF | GRCh38.p7 | 16:2432941 | TCCATCACCCAGCCC[C/T]GGCCCCCGTTGTTCT | 899 |
rs554271710 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2441628 | AACCTCTGACGCCTG[G/T]GTTCAAGCCTTCTGA | 899 |
rs554274280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2449988 | GAGGCGGGCAGATCA[C/T]TTGAGGTCAGGAGTT | 899 |
rs554321667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433607 | TTTGTTTTTTTCTTG[A/G]GACGGAGTCTCGCTC | 899 |
rs554344820 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2455331 | TTAGAGGCAGGTGTG[G/T]AGGGCCTGGCCTCCC | 899 |
rs554382376 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457550 | TGGGTGGGGCTTCCA[C/T]GGTAAGGGGGCCTGC | 899 |
rs554646680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447300 | TTTTTTTTTAAATCC[A/G]GGGACCAGGCACGGT | 899 |
rs554717212 | snp | C/T | | | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2431218 | GACCATCTTGAGTCT[C/T]CCCGAAGATGTGCTC | 899 |
rs554772897 | in-del | -/TG | 0.00597247 | 0.0543191 | intron-variant | CCNF | GRCh38.p7 | 16:2442806 | ATATTCTATAATATA[-/TG]TAATATATTCTATAA | 899 |
rs554838007 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CCNF | GRCh38.p7 | 16:2455733 | GTCCAGACATGGGGA[A/G]AGAGGAGGGGAGAGC | 899 |
rs554929525 | snp | A/C | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427699 | CACACCCTGGAGGAG[A/C]CACTTATCACCCCAG | 899 |
rs554987839 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CCNF | GRCh38.p7 | 16:2451766 | TCCCTCGGGGGCTTC[A/G]GCTTCCTGCCCTAGG | 899 |
rs555221473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450109 | CTACTCAGGAGGCTG[A/C]GGCAGGAGAATCGCT | 899 |
rs555349730 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2437615 | CAAATCTGGCCAGGT[A/G]TGGTGGCTCACGCCT | 899 |
rs555425979 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457973 | GAAGAGCAGAGCAGT[C/T]GGGGGCCGTGTCCTG | 899 |
rs555457340 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2447913 | GGCAGGTGTAGTCCC[C/T]GCGCCTCTTGTCCTC | 899 |
rs555465125 | snp | C/T | 4.96044e-05 | 0.00497993 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453499 | CACAGGGGAGATCCA[C/T]GCCTTCCTCAGCTCT | 899 |
rs555485972 | in-del | -/ATA | | | intron-variant | CCNF | GRCh38.p7 | 16:2442457 | ATATAATATTATATA[-/ATA]TAATATTATTATATA | 899 |
rs555648419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2440416 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 899 |
rs555811267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443901 | TTACCTGTGACAGGG[C/T]GGCATAGAGTTCCCT | 899 |
rs555847401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446169 | GGTGCCTGCATCCAG[A/G]CAATTCATCCTGGCA | 899 |
rs555892403 | snp | G/T | | | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456800 | GTCCCACAAGCTCCG[G/T]GGACGGTGGCTTGGG | 899 |
rs555999924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437667 | GCCGAGGCTGGAGAA[C/T]TGCTTGTGGCCAGGT | 899 |
rs555999972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2431526 | CTCTACTAAAAATAC[A/G]AAAATTAGCCGGGCG | 899 |
rs556103313 | snp | C/G | 5.73214e-05 | 0.00535326 | intron-variant | CCNF | GRCh38.p7 | 16:2433097 | TGAGAATGGCTCAGT[C/G]TTCTCCTGCCTTGGC | 899 |
rs556184434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2439979 | AAGATCGGTTCAGCA[C/T]TGGAACTGGTCCTAA | 899 |
rs556264911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438414 | CTGGCCCTGCTCCTC[A/G]TGGGCCTCTCCTGCT | 899 |
rs556367468 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CCNF | GRCh38.p7 | 16:2435159 | GGGAGGCTGAGGCAG[C/G]AGAATGGTGTGAACC | 899 |
rs556382714 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445171 | TGTGGGCAGACCAAC[A/G]GCTGTGGGCTGACTT | 899 |
rs556402032 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428019 | GGGGGAGACAGGTAA[A/C]AGTGACAAAGTAGGA | 899 |
rs556423009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446578 | ACCAGCTGTCCCCAG[C/T]ATGGTCTACATTTCC | 899 |
rs556548653 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2430784 | CTGAGAGTGAAATAG[A/T]AGGAAAACCGTCCTC | 899 |
rs556673919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2436257 | CGAGACAGAGTTCAG[C/T]GTGCCCTGTAACACA | 899 |
rs556814699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2443148 | ATGTTTTATATTGTA[C/T]ATAATATATATTATA | 899 |
rs556918998 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458501 | GTGATCCGCCCACTT[C/T]GGTCTCCCAAAGTGC | 899 |
rs557016776 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CCNF | GRCh38.p7 | 16:2442449 | TATATAATATATAAT[A/T]TTATATAATATAATA | 899 |
rs557346338 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457362 | CCCCACCAGAGCCCC[A/G]TGCCGGGAGCTGACA | 899 |
rs557385100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447339 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGATG | 899 |
rs557511212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2454857 | CTGAAGTTAGGAGTT[C/T]GAGACCAACCTGCCC | 899 |
rs557533283 | snp | A/C/T | 7.43859e-05 | 0.00609821 | utr-variant-5-prime, missense, synonymous-codon | CCNF | GRCh38.p7 | 16:2437289 | CAAGGCCGTGGTTCA[A/C/T]GAGAGCCTCAGGGCA | 899 |
rs557538528 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428928 | CCGGGCAGGGCACGG[C/T]CTCGTCTTAGAAGCG | 899 |
rs557664903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452453 | ATGGGGAGCACAGAT[C/T]GTCCCAACCCTGGCC | 899 |
rs557829888 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440992 | TAATGCCAGCACTTT[A/G]GGAGGCTGAGGCGGG | 899 |
rs557845567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2449115 | TGTGCCCAAAGCCAT[A/G]GAGCAGGAGGCCACG | 899 |
rs558085208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447156 | GCTGGCAGTGAGAGA[A/G]TAACTGCTAAAAACG | 899 |
rs558092070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443950 | TTTGAAGTGGAGTCT[C/T]GCTCTGTCGCCCAGG | 899 |
rs558100872 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2450526 | AAAAAAAAAAAAAAA[G/T]TTCCAGTAGTTTCTT | 899 |
rs558165149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444394 | AAGCTCCACCTCCCG[G/T]GTTCACACCATTCTC | 899 |
rs558248761 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2452269 | CTGCTTTTTCTCCCA[C/G]CATGCTGTGCTCCAG | 899 |
rs558250394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446709 | TTCTTGCACAGGTAA[C/T]CCAGAGGCAGAGGTT | 899 |
rs558357760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432443 | GTGGAAACTTTGGTG[C/T]TTAAAGTGTTCACCT | 899 |
rs558396569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432852 | AACTACTTGGGATGG[C/T]GAGGGAGACAGGAGA | 899 |
rs558440437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2436175 | GGGCTCCCTGCCCTG[C/T]GCGCCATGAGCACGC | 899 |
rs558488803 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428003 | GTGCACCTCTGCCCT[A/G]GGGGGAGACAGGTAA | 899 |
rs558682098 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CCNF | GRCh38.p7 | 16:2451147 | CATGAAGTCCCTACC[A/G]TGGTCCAGGCGCTGG | 899 |
rs558706081 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2453806 | ATGGTTTCGAGCACG[C/T]GGGAGCCTAGCCTGG | 899 |
rs558756955 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429058 | TCTGGCACCGCAGAT[A/G]CCGGTCGCCGGGGTC | 899 |
rs558778610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2439129 | ATGGTGAAACCCCGT[A/C]TCTACTAAAAATACA | 899 |
rs558792335 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2429717 | GCCCCTCGGAGCCTT[A/C]CCCCGCGGCGACGTT | 899 |
rs558809627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2441570 | CCAGGAGTTCTCTCT[G/T]TTGCCCAGGCTAGAG | 899 |
rs558815257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433733 | TAGGATTACAGGCAC[A/G]CGCTACCACGCCCAT | 899 |
rs558845158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2435624 | ATATGCACACACACA[A/C]ACACATATATATGCA | 899 |
rs559096205 | in-del | -/T | 0.494358 | 0.0528145 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443924 | GTTCCCTTATCACCC[-/T]TTTTTTTTTTTTTGA | 899 |
rs559133661 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2458086 | TGCTCCTGCATGGAA[A/G]GGGAGCCTGGGAGCC | 899 |
rs559137642 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2438510 | GCTGGGCGTGGTGGC[A/G]GGTGCCCATAATCCC | 899 |
rs559207587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448253 | ACGTGACAGGCAAAT[C/T]TCTGTCCTTGGTGTC | 899 |
rs559244938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448797 | GCCTTGGGTCCCTCC[G/T]CCCCACCCCTGCCCC | 899 |
rs559414280 | snp | A/G | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443462 | TTTCTCATGTCATCT[A/G]TTACTTATACAAAAA | 899 |
rs559613342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452510 | TATTCTCTTCCTCCT[A/G]AAGAAGTTAATTTTT | 899 |
rs559658134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2436302 | AACGGGAAGCAGGTA[C/T]AGGCAGGTTAGAACT | 899 |
rs559742640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447384 | GGTCAGGAGTTCAAG[A/G]CCAGCCTGGCCAACA | 899 |
rs559781420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452115 | TCCGTGGCGGCTGCC[C/T]GGCCTCCTGGAACAC | 899 |
rs559863501 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429336 | CGGCGGCCCCCCCGG[G/T]CAGGCCAATGGGAGG | 899 |
rs559907672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446939 | CTGTGTGTGCCAGCT[C/T]GATGCAGTGTCATTC | 899 |
rs560175428 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2454487 | CCCGCTTCTCAGAGG[-/C]CCCCCACAGCCCCAT | 899 |
rs560215143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433320 | GGTGCCTCCAGAGGG[C/T]TGTGATCCATTCCCA | 899 |
rs560216391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2450182 | ACTGGACTCCAGCCT[A/G]GGTGACAGAGCAAGA | 899 |
rs560256570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2431871 | AGTCTCGCTCTGCCA[C/T]CCAGGCTGGAGTGCA | 899 |
rs560302997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444704 | CAAGCTCAAGAGATC[C/T]TCCCACCTTACCCTC | 899 |
rs560364056 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2441183 | AAGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC | 899 |
rs560386088 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459018 | TGGGTGGGTTCCTGC[A/G]TCACCCACCTGCTGA | 899 |
rs560411559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437446 | AGTGAAGATGCAGAA[A/G]ACTGAGAGTGCAGAT | 899 |
rs560472358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2439276 | GCACTCCAACCTGGG[C/T]GACGAGTGAAACTGT | 899 |
rs560569155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454648 | ACACACTGGCCTCTA[A/G]CCCCATCCTGAGCAA | 899 |
rs560577886 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2452070 | TCAGTGCAGTTTCCT[C/T]GTGCGCTCACAGCTT | 899 |
rs560626836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436996 | CATCCTGGAGGGCTC[A/T]ACTCTCCTGAAACAC | 899 |
rs560665712 | snp | A/G | 4.94181e-05 | 0.00497057 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431196 | TAAGGAGGAGGCCCC[A/G]AAACCTGACCATCTT | 899 |
rs560721797 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429136 | CCCTGCCCGCCGGCC[A/G]GGAAGCGCTCCTACG | 899 |
rs560815223 | snp | C/T | 1.6679e-05 | 0.00288777 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456750 | GCCAGGGAAGGACGT[C/T]ACGACCTCAGGGTAC | 899 |
rs560852953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2454209 | CAGAAGCGTTGTGTC[A/G]GGAGTGGGCTCCTGG | 899 |
rs560955732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2435192 | GGAGGCGGAGCTTGT[A/G]GTGAGCCGAGATTGC | 899 |
rs561027143 | in-del | -/ACAG | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2451452 | TCCTCAGCTGTGCTC[-/ACAG]ACTTGCTCCTCCCAC | 899 |
rs561175448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450819 | TGAGCTCATAGTGCA[A/G]CGGACACCACGTGGC | 899 |
rs561176335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452592 | ATTGTGTGATTTAAC[A/G]GGCTTTTATTCACAC | 899 |
rs561201132 | snp | C/G | 1.85094e-05 | 0.0030421 | intron-variant | CCNF | GRCh38.p7 | 16:2449492 | TTCCCAGGGATGCCT[C/G]TGTCGGGGAAGGTGC | 899 |
rs561612863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2451226 | ACAGCAGGCAGGCGC[A/G]CGGGGCAGGTGGCGC | 899 |
rs561639647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446307 | GTTGGCTGCCCTTCT[C/G]TGAAGTTGGGTTCTA | 899 |
rs561705267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2454093 | TGCTGCTGGCCCTGC[A/G]CCGTGACCCCTCAGC | 899 |
rs561729513 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458232 | AGAAAGAACCACTTG[G/T]CCAGAAGTGTCCCCC | 899 |
rs561786174 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2436082 | GCAGGTTACGAAAGT[C/T]GCCTCTTGTTTTAGC | 899 |
rs561811586 | snp | A/G | 0.00436963 | 0.0465373 | intron-variant | CCNF | GRCh38.p7 | 16:2449181 | GCGTGCAGCATCGGC[A/G]TGAACATCATCCGGG | 899 |
rs561849826 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2432879 | GAGACCCTACATCTG[C/T]CTCTCGTCCTCAAGA | 899 |
rs561858278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444161 | CCTGACCTCGTGATC[C/T]GCCCGCTTTGGCCTC | 899 |
rs561882999 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444494 | TTTAGTAGAGATGGG[C/G]TTTCATCGTATTAGC | 899 |
rs562005808 | snp | A/G | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457367 | CCAGAGCCCCGTGCC[A/G]GGAGCTGACAGCTTT | 899 |
rs562028369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452952 | GCTGGTGGACATTTT[A/G]CCTATTGTGAACAGT | 899 |
rs562107942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2430956 | TGTGCAATGCCACTC[C/T]TTTACATAATCTTTG | 899 |
rs562145171 | in-del | -/TTT | | | cds-indel, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458269 | TTTTTTTTTTTTTTT[-/TTT]GGAGACAGTTTTGCT | 899 |
rs562188116 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447508 | AGAATTGCTTGAACC[C/T]GAGAGGCAGAGGTTG | 899 |
rs562221447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450613 | GGCAGCAGAACATAC[C/T]AGAAAAAATGAGGGC | 899 |
rs562354596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454731 | CCATGCAATCTGCCT[C/G]GCGCCGGGCTAAGCA | 899 |
rs562357902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436377 | TTGAAAGAAACTTGC[A/G]CAGCCTTTTCTTCTA | 899 |
rs562393667 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2436919 | CACAGCAGGGGCATT[A/G]ATCACAATGACCCAC | 899 |
rs562462008 | in-del | -/GGCACAGGCTGGACTGCCCTGTCCCCTGGCTCCTGAG | 0.0221141 | 0.102801 | intron-variant | CCNF | GRCh38.p7 | 16:2446223 | GGCCTCGCTCTGGCA[lengthTooLong]GGCAGCAGGATGACT | 899 |
rs562594297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438703 | GTGATTGAACATCAA[A/G]TAAAGAATAAGGGCC | 899 |
rs562610807 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2452391 | GGCAAGGAACGAGGC[G/T]GACAGTAGAAGGGTT | 899 |
rs562639566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2431980 | GGACTACAGGCACCC[A/G]CCACCACGCCCGGCT | 899 |
rs562641518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437803 | ACTCAGGAGGCTGCG[G/T]TGGGAGGATCGCTTG | 899 |
rs562645880 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454526 | TGAGACAGACCCCCA[C/T]GGGTGACACTGGGAT | 899 |
rs562678472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432514 | GCGCTTAGGCTCCGG[G/T]TTCTACCTGAGACCT | 899 |
rs562844091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455039 | CACTCTAGCCTGGGC[A/G]ACAGAGCAAGAACAC | 899 |
rs562929497 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CCNF | GRCh38.p7 | 16:2437692 | CCAGGTGTTCGAGAC[C/T]AGTCTGGGCAACATG | 899 |
rs562980772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450240 | CATGGTGGCTCACAC[C/G]TGTAATCCCAGCACT | 899 |
rs563045067 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444927 | TTTGAGGCAGGCTGT[C/T]TGTCACCCAGGGTGG | 899 |
rs563208961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452670 | CCCCAAAGGGACAAC[A/G]CACCCCTCAGCTGTC | 899 |
rs563247735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453017 | GGACATAGTTTTTCC[C/T]TTTTCCTGGGTCTTT | 899 |
rs563403314 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457616 | GCCCACTCCCTACGA[C/T]ACGTGACTCGTTTTA | 899 |
rs563498920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2435327 | TCAAGCCTATAATCC[C/T]AGCACTTTATGAGGC | 899 |
rs563541314 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2456161 | TCTAGAATGTTGTTT[-/G]AGGTGTGCCCACGTG | 899 |
rs563578296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2446408 | AGCCCACTCCAGCCA[C/T]GTGGGTGTCTCTCAG | 899 |
rs563691989 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2441769 | TAATCTGCCCTCCTC[A/G]GCCTCCCAAAGTGTT | 899 |
rs563726993 | in-del | -/GA | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2436522 | CTGGTGTCTTGCTGG[-/GA]GAGAGTCCCTACCTG | 899 |
rs563737914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2456005 | AGCAAGACAAAAAAT[C/T]TAAAAATTAGCTGGG | 899 |
rs563777257 | snp | A/G | 1.92469e-05 | 0.00310211 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456559 | GTGACAGCTCCCAGC[A/G]GCATCCTCGATGTCA | 899 |
rs563897079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432611 | CTCCAGCGGGGAAGC[A/G]CAAAACACATTTCCG | 899 |
rs563915133 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438375 | ATCTCAAGGAGGCAT[C/T]GAACCTCGATGCTCA | 899 |
rs563970926 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441569 | GCCAGGAGTTCTCTC[G/T]GTTGCCCAGGCTAGA | 899 |
rs564030415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2441105 | TGGGCCTGGTGGCAT[A/G]TGCCTAGAGTCCCAG | 899 |
rs564152210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454185 | TATAGGACCAGGCAG[A/G]GCTGCCTCCAGAAGC | 899 |
rs564207647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444542 | CCTGACCTCGTGATC[C/T]GCCTGCCTCCGCCTC | 899 |
rs564220287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448634 | GCCCAGGGTGGTCTC[A/G]AACTCCTGGCTGAGC | 899 |
rs564243207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437891 | GTGACAGAGCAAGAC[C/G]CTGTTTCCCTTTAAA | 899 |
rs564282038 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436971 | TAGGGGGAGAAAAGA[C/G/T]AGGTGCCCCCATCCT | 899 |
rs564358683 | snp | A/G | 1.81737e-05 | 0.00301439 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445656 | CCAGCTGGCAGGGAC[A/G]TGCTGGCCTTTCCCG | 899 |
rs564586946 | snp | A/T | 0.137187 | 0.223099 | intron-variant | CCNF | GRCh38.p7 | 16:2442470 | TAATATAATATTATT[A/T]TATATAATATATAAT | 899 |
rs564631141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446251 | CTGCCCTGTCCCCTG[G/T]CTCCTGAGGGCAGCA | 899 |
rs564803492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2431717 | GGGCAAAAAGGAAAC[A/C]AGGATGATATCATTA | 899 |
rs564810369 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458394 | GTAGCTGGGATTACA[A/G]GCACCCAACCACGCC | 899 |
rs564864621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434850 | GGATTTCACATGGAA[C/T]CATGCAACACGTGGT | 899 |
rs565045507 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CCNF | GRCh38.p7 | 16:2429998 | CACGAACTGTGGTTT[C/T]AGCTATTATCATAGT | 899 |
rs565092752 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445804 | GCGATCTTGGCTCAC[C/T]GCAACCTCTGCCTCC | 899 |
rs565131831 | snp | A/C | 0.000334348 | 0.0129252 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456697 | ACCCAGATCCCTGCA[A/C]CCCCTGGACCCAAAC | 899 |
rs565219861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450311 | CAAGACCAACCTGGT[C/T]AACGTGGCAAAACCC | 899 |
rs565257877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2450724 | GGCATCTGGCTGCTT[C/T]TGCGAATGGGGTTTT | 899 |
rs565356514 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | CCNF | GRCh38.p7 | 16:2438825 | AATGTGTTGAAACCA[A/C]GTCTTTACTAAAAAA | 899 |
rs565384799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447778 | AAGATTTTAAAGGCT[A/G]AGCTGCCCCCCACCT | 899 |
rs565449010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447180 | AAAAACGTTTCAGGG[A/C]GCTGAGTCCAATTTC | 899 |
rs565613662 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457251 | AAAGTTTAGCCTGGA[A/C]GCAGTTGGCCACACT | 899 |
rs565653302 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | CCNF | GRCh38.p7 | 16:2442759 | ATAATAATTATAATA[A/T]TATAATATATATCAT | 899 |
rs565690129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436463 | AGCTCTCAAAACAAG[C/T]AAACACTGGGATGTA | 899 |
rs565742076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452292 | TGCTCCAGCCACAGG[A/G]GACCTGGTGGCATCT | 899 |
rs565892735 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2455288 | GAACCTTTGGGAGCA[C/T]GTGGTGACAGGCTGG | 899 |
rs566018248 | snp | A/G | 5.25463e-05 | 0.00512546 | intron-variant | CCNF | GRCh38.p7 | 16:2439852 | GGGCTGGGATGACGT[A/G]GGGAGCTGGCCTTTC | 899 |
rs566019477 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2435020 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 899 |
rs566156853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446504 | AATGCTGGATCCCCT[A/G]GTTCCGCCTTTGGAA | 899 |
rs566180951 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2440347 | GTTAGGGCCAGGTGC[A/C/G]GTGGCTCACGCCTGA | 899 |
rs566236538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2435486 | GCTACTTGGGATGCC[A/G]GGGTGGGAGAATGGC | 899 |
rs566273888 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428601 | CGCGGCGAGCAGCTC[C/T]AGGTAGCAGCCGAGG | 899 |
rs566297845 | snp | C/T | 1.65353e-05 | 0.00287531 | synonymous-codon, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456846 | TACCTCAGTGCTGTC[C/T]CTGGACAGTGACTCG | 899 |
rs566508235 | snp | A/G/T | 8.31234e-05 | 0.0064463 | intron-variant | CCNF | GRCh38.p7 | 16:2453571 | TGGCTGCGCCATACA[A/G/T]TGCTGGCATCCTCGT | 899 |
rs566517527 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457954 | CTGAGGTGACCAAGA[A/G]GCAGAAGAGCAGAGC | 899 |
rs566575807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454788 | AGAGGGGCCGGGTGC[A/G]GTTGCTCATGCCTGT | 899 |
rs566746197 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432675 | TCTTTGGGGGTGATA[A/C]CTTTGCAGGGATGTT | 899 |
rs566884441 | snp | G/T | 1.65326e-05 | 0.00287507 | missense | CCNF | GRCh38.p7 | 16:2453477 | CCGACCCCCCGACTT[G/T]CCTCAGCACAGGGGA | 899 |
rs566913034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455682 | GATGTGCACAGAGTG[C/T]GGGGTGGGGCCAGCT | 899 |
rs567107345 | snp | A/G | 3.36395e-05 | 0.00410105 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443848 | GCGGCGCGGAAGCCA[A/G]CCTCCAGGGGAAGGG | 899 |
rs567312730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447322 | AGGCACGGTGGCTCA[C/G]GCCTGTAATCCCAGC | 899 |
rs567433126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445131 | TCCCGCTCCCTGCAC[G/T]CCCCGAGGGTCAGGG | 899 |
rs567445248 | in-del | -/CA | 0.364193 | 0.222396 | intron-variant | CCNF | GRCh38.p7 | 16:2442682 | TATTATATATAATAT[-/CA]TATTATTATATAATA | 899 |
rs567448300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2452185 | AGGGCCTCGCTGTCC[A/G]GCTTCCAGGATGAGA | 899 |
rs567516159 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2451565 | CTCAGCGGTGTGGGC[A/T]TTTTTTTCCTTTTTT | 899 |
rs567562890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446564 | TTTGCATTTCCTAAA[C/G]CAGCTGTCCCCAGCA | 899 |
rs567581765 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2448149 | CAGACTTTCCAACAA[C/T]CCTTGGGCCCTTTGC | 899 |
rs567594764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445872 | AGCTGGGACTGCAGG[C/T]GTGCGCCACCATGCC | 899 |
rs567617845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2449989 | AGGCGGGCAGATCAT[C/T]TGAGGTCAGGAGTTT | 899 |
rs567633537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2439614 | AGTCGGCTATTCTTG[G/T]TACCCCCAAAAATGA | 899 |
rs567654269 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2446144 | TCAGCGTGTGGGGGC[C/T]GCTGTGTGGGGTGCC | 899 |
rs567799677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434196 | TTGTAGTCCCAGCTA[C/T]TCTGGAGGCTGAAGC | 899 |
rs567887159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433618 | CTTGAGACGGAGTCT[C/T]GCTCTGTCACCAGGC | 899 |
rs567999121 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2436563 | CAGAATTGTGACTGA[A/C]AGGGACCATGAGCAA | 899 |
rs568010786 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CCNF | GRCh38.p7 | 16:2442933 | TATTAATATATATGA[A/T]TATTATATATTATTA | 899 |
rs568035415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437039 | CTATGGTGGGCTTCA[C/G]GCATTACACTTTCCA | 899 |
rs568038188 | in-del | -/CTTAA | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B, upstream-variant-2KB, nc-transcript-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458902 | CCTTGTCCAGGGGCT[-/CTTAA]CTTAATCCCAACTCT | 899 |
rs568039172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2430673 | TTTGGACTTGAAAAC[C/G]AGACTCTTCAAGCCC | 899 |
rs568096411 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2437327 | AGCTGCAGAGGGTGA[A/G]TCTGGGCGAGGGGCA | 899 |
rs568199493 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2429769 | ACGATCGGGTCCCGG[A/G]GCAGCGATCCGGCGA | 899 |
rs568403979 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428880 | CGTGCAAGCTGGGGG[G/T]GAGGGTCGCGGGCCC | 899 |
rs568425686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436066 | ATGATACTCTGACTT[C/T]GCAGGTTACGAAAGT | 899 |
rs568591972 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2435548 | TGTGATCGCACCACT[A/G]CACTCCAGCCTGGGC | 899 |
rs568662712 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457295 | CTCTCTGTCCCTTCC[A/G]TGTCTCACTGTCTCT | 899 |
rs568697259 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457767 | AGATGAAAACAAAAG[A/G]AAAACTTAAAACAGA | 899 |
rs568857990 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2455133 | GGACCAGATGGTTGG[C/T]CCACGCCCCACAGCT | 899 |
rs568870077 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458735 | TGGAACTGTAGACCC[A/G]TCCTGTCGACTGTGT | 899 |
rs568902785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453830 | AGCCTGGCTCTAGCC[C/T]TGCCCGTGCCTGTCA | 899 |
rs568904965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459127 | GGAGGGGCCCACCCG[A/G]AGCGCTGGGCCAGAG | 899 |
rs568963761 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458470 | GGCCAGGCTAGTCTC[A/G]AACTCATGACCTCAA | 899 |
rs568993817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432775 | ACCTCAGAGAAACTC[A/G]TTTCTGGGCTCTTTT | 899 |
rs569066021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455313 | GGCTGGGGCACGCGG[C/G]TGTTAGAGGCAGGTG | 899 |
rs569096312 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2448840 | CCACCCTGAGACCCC[C/T]TCTCGGCGTTGCAGG | 899 |
rs569102700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450459 | GAGGTTGCGGTGAGC[C/T]GAGATTGCGCCATTG | 899 |
rs569104530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455622 | AGGGTGGCTCTCACC[A/G]AGGGCCTCTGGGCAC | 899 |
rs569382499 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2456289 | TCCTGTCAGTTTCCC[A/G]GTTGCTTGCTTCTGC | 899 |
rs569460165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444390 | CTGCAAGCTCCACCT[C/T]CCGGGTTCACACCAT | 899 |
rs569481327 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444781 | GTTGTATTTTTAGTA[A/C/G]AGACAGGGTATCACT | 899 |
rs569518039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437678 | AGAATTGCTTGTGGC[C/T]AGGTGTTCGAGACCA | 899 |
rs569537585 | snp | A/G | 0.000428266 | 0.014627 | missense | CCNF | GRCh38.p7 | 16:2449893 | GACCTCATTCCCTGC[A/G]TCTTGAGCCTCCATA | 899 |
rs569659166 | snp | C/T | 6.63042e-05 | 0.0057574 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456798 | AAGTCCCACAAGCTC[C/T]GTGGACGGTGGCTTG | 899 |
rs569794958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2442143 | CCCAAGTAGCTGGGA[C/G]TACAGGCATTGCACC | 899 |
rs569871338 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427583 | CTACCCATAACGTTT[C/T]CAACCGACACCTCAT | 899 |
rs569911553 | snp | G/T | 0.314544 | 0.241524 | intron-variant | CCNF | GRCh38.p7 | 16:2435600 | AGAGAGAGAGAGATA[G/T]ATATATATATATGCA | 899 |
rs570032862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434980 | AAATGTTCGACCGAG[C/T]GTGGTGGCTCACGCT | 899 |
rs570078752 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2439778 | GCGATGCCTCCACAG[C/T]TTCCGAAAACTCAGG | 899 |
rs570132919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450873 | TTCCCTTGAGAGAAC[A/G]GCTTCTGCCCTGATG | 899 |
rs570142023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2445972 | TGATTTCAAATGATC[C/T]GCCCGCCTCAACCTC | 899 |
rs570238442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2440229 | CTGCTTCCTCTTCCT[C/G]TTAGCGCCTTGCTTG | 899 |
rs570327856 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434397 | AGGCGGGCGGATCAC[A/G]AGGTCAAGAGTTTGA | 899 |
rs570433535 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432075 | GACCTCGTGATCCGC[A/C]CGCCTCGGCCTCCCA | 899 |
rs570537403 | in-del | -/ACCCC | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2439121 | GGCCAACATGGTGAA[-/ACCCC]ACCCCGTCTCTACTA | 899 |
rs570587956 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459259 | ATCTTTAAACAGCAA[C/T]CCCAGGCTCTGTTTT | 899 |
rs570839573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436148 | GCCAGAGCCTCAGCA[C/T]GGGGGCTGTTTGGGC | 899 |
rs570856387 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457368 | CAGAGCCCCGTGCCG[A/G]GAGCTGACAGCTTTC | 899 |
rs570979566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2429575 | GGACGGTGGGTCCCG[C/G]GGGAGGGGAGGCCCT | 899 |
rs571101509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453637 | GAGGCCCCCAAGGCT[C/T]GTCAGGGGAGCAGCA | 899 |
rs571101799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448342 | CTAACAGCCTTGCTG[C/T]TTTCTGTCTGCCTTG | 899 |
rs571131773 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454797 | GGGTGCGGTTGCTCA[C/T]GCCTGTAATCCCAGC | 899 |
rs571190447 | snp | A/G | 9.28836e-05 | 0.00681419 | intron-variant | CCNF | GRCh38.p7 | 16:2455353 | TGGCCTCCCAGCGCC[A/G]CCGTCCATGACTGGG | 899 |
rs571305213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2453804 | AGATGGTTTCGAGCA[C/T]GCGGGAGCCTAGCCT | 899 |
rs571310681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2433508 | TGGTCCCAGGTACCC[A/G]CCGCCCTCAGAACAA | 899 |
rs571353473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2449972 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 899 |
rs571397820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2451396 | TGAGGGGGACAAGCA[C/T]GGGGCTGAATTTGTA | 899 |
rs571492464 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CCNF | GRCh38.p7 | 16:2455649 | GCACCCGGCCCTGTG[C/T]GAGCGCTGTGGGAGG | 899 |
rs571508293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446073 | AGTGTCCCACCTGGT[C/G]AGACATGGAGTGCCA | 899 |
rs571588465 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445032 | AGTAGGACTACAAGT[A/G]TCTCCACTCTATTCA | 899 |
rs571630614 | in-del | -/GCGATCCGGCGATCGGGTCCCGGGGCG | 0.0729998 | 0.176553 | intron-variant | CCNF | GRCh38.p7 | 16:2429773 | TCGGGTCCCGGGGCA[-/GCGATCCGGCGATCGGGTCCCGGGGCG]GCGATCGGGTCTCGG | 899 |
rs571706507 | snp | G/T | 8.91305e-05 | 0.00667513 | intron-variant | CCNF | GRCh38.p7 | 16:2432916 | AGGTGTGGGGCTTTT[G/T]GGTGGTGCCTCCATC | 899 |
rs571784381 | in-del | -/A/AA | | | intron-variant | CCNF | GRCh38.p7 | 16:2455057 | GAGCAAGAACACCTC[-/A/AA]AAAAAAAAAAAAAAA | 899 |
rs571862675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438281 | CCAGGGGACACATGT[C/G]GGCCTGGCCACGGGC | 899 |
rs571951905 | in-del | -/T | 0.307919 | 0.243198 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458254 | GTGTCCCCCAGATGC[-/T]TTTTTTTTTTTTTTT | 899 |
rs572023503 | in-del | -/TCC | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2448652 | CTCCTGGCTGAGCTG[-/TCC]TCCTGCCTGGGCCTC | 899 |
rs572047867 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2435229 | GCACTCCAGCCTGGG[C/T]AACAGAGCAGACTCC | 899 |
rs572221317 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456944 | AGAGCAGTGTTCCCC[A/G]GCAACAGGTGAAGCG | 899 |
rs572293250 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2434430 | CCAGCCTGAGCAACA[A/T]GGTGAAACCCTGTCT | 899 |
rs572330956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446269 | CCTGAGGGCAGCAGG[A/T]TGACTGATCAGGGAG | 899 |
rs572426834 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2433649 | TGGAGTGCAGTGGTG[C/T]AATCTCAGCTCACTG | 899 |
rs572461167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2434587 | CTGCACTCCAGCCTG[A/G]GCAACAGAGCGAGAC | 899 |
rs572551126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456401 | GAGGCATGTCACCCA[C/T]GCTTCTCACCACAGG | 899 |
rs572589334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2451676 | TTGTGTCAGCCTCCC[A/G]AGTAGCAGAAACCAC | 899 |
rs572600364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2451158 | TACCGTGGTCCAGGC[A/G]CTGGGGGAGAGGGCA | 899 |
rs572737768 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444065 | GCTGGGACTACAGGC[A/G]CCCACCACCATGCCC | 899 |
rs572852534 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458182 | GACCACAACACACCC[C/T]GCTGCCATCCACTTC | 899 |
rs572909112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2431475 | CCTGAGGTCAGGAGT[C/T]CCAGACCAGCCTGGC | 899 |
rs572984628 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2454431 | GGCTACTCCAGGAGG[A/G]GGCCTGGCCCTGGCC | 899 |
rs573143147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452929 | CACATGTGTTTATCC[A/G]TCCCGCAGCTGGTGG | 899 |
rs573240152 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2452567 | TTATTTAGAAACTAC[A/C]CTTCCTTTGATTGTG | 899 |
rs573416683 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441342 | TCAAAGCTGCAGAGA[G/T]CCGTGATCGCAACAT | 899 |
rs573446679 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2448463 | CCAGGTTGGAATGCA[G/T]TGGTGTAATCAAAGC | 899 |
rs573493084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436309 | AGCAGGTACAGGCAG[C/G]TTAGAACTGGCCTGG | 899 |
rs573552571 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | CCNF | GRCh38.p7 | 16:2442461 | AATATTATATAATAT[A/T]ATATTATTATATATA | 899 |
rs573572263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450593 | CAACCCAAGCTCATT[A/G]CACAGGCAGCAGAAC | 899 |
rs573590509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2443359 | GCGTATGGCCAGAGA[C/G]TTAACACAGCTTCCC | 899 |
rs573591758 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2449020 | TAATCTTCGTTGTCG[A/C]TGTGCTGGAGGGTGG | 899 |
rs573616639 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445718 | TCACTGGTTTGGTTT[G/T]GTTTTGTGTTGTTTT | 899 |
rs573826067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446134 | AGAACAGCCTTCAGC[A/G]TGTGGGGGCCGCTGT | 899 |
rs573912796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454937 | TGATGGCGGGCACCT[A/G]TAGTCCCAGCTACTC | 899 |
rs573934478 | in-del | -/A/AA | 0.495521 | 0.0471118 | intron-variant | CCNF | GRCh38.p7 | 16:2437903 | ACCCTGTTTCCCTTT[-/A/AA]AAAAAAAAAAAAAAA | 899 |
rs573956085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2439280 | TCCAACCTGGGCGAC[A/G]AGTGAAACTGTCTCA | 899 |
rs573965243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456434 | GGTAACACAGGGGAC[C/T]GTAGCAAGGTAGAAG | 899 |
rs573995838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433751 | CTACCACGCCCATCT[A/G]ATTTTTGTATTCTTA | 899 |
rs573998478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432501 | CTGCGTTGGCCCAGC[A/G]CTTAGGCTCCGGGTT | 899 |
rs574143678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436200 | GCACGCAGACCTGCC[C/T]GTGGATGCTGGCCCT | 899 |
rs574205402 | snp | A/T | 0.151334 | 0.229706 | intron-variant | CCNF | GRCh38.p7 | 16:2442434 | AATATAATATTATTA[A/T]ATATAATATATAATA | 899 |
rs574261584 | snp | A/G/T | 0.00100462 | 0.0223922 | intron-variant | CCNF | GRCh38.p7 | 16:2432942 | CCATCACCCAGCCCC[A/G/T]GCCCCCGTTGTTCTG | 899 |
rs574271713 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457580 | CGTCCCTGCACACTG[C/T]GAGGACTGCCTTGGC | 899 |
rs574309783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452991 | GAACATTCTAGTACA[G/T]GTTTCTGTGTGGACA | 899 |
rs574419474 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429189 | GCGGGGCGGCCACGC[A/G]GGTTCCACCAATCAG | 899 |
rs574448430 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2431553 | GGCGTGGTGTCTCAC[G/T]CCTGTAATCCCAGCT | 899 |
rs574631247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2429868 | TGCGGAGCGCGTGGG[A/G]GCGAAGCGATCCCGC | 899 |
rs574632819 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2451644 | CAGCCCTGACCTCCC[A/G]GGCTCAAGGGATTCT | 899 |
rs574725344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2441005 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACGAGGT | 899 |
rs574867216 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2455965 | TCACTTCAGGCTAGA[A/T]GTTCAAGACCAGCCT | 899 |
rs574904284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456435 | GTAACACAGGGGACC[A/G]TAGCAAGGTAGAAGA | 899 |
rs574970935 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2435079 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 899 |
rs574972537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446779 | AAGCAGAGGAGCCCC[A/C]TCTCCCATCTTAATC | 899 |
rs575031304 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2451831 | CACCCCAAGGGGCCC[C/T]GGAATTCTGGCTTTC | 899 |
rs575303360 | snp | C/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428104 | GAGAACATGGGACAT[C/T]TGGGGAGCAGGCCCC | 899 |
rs575327635 | in-del | -/AGCT | 0.00279273 | 0.0372635 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444510 | TTCATCGTATTAGCC[-/AGCT]AGGATGGTCTCAATC | 899 |
rs575344019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454490 | GCTTCTCAGAGGCCC[C/T]CCACAGCCCCATCAG | 899 |
rs575369544 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458742 | GTAGACCCGTCCTGT[C/G]GACTGTGTGCCCCTG | 899 |
rs575426572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445196 | TGACTTTTCACTTTG[C/T]GTCAGGTCGAGGTCT | 899 |
rs575482682 | in-del | -/CTG | | | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446860 | ACATTCACCTTTGCA[-/CTG]CTGAGCTTAGTCTTG | 899 |
rs575502206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450129 | GGAGAATCGCTTGAA[A/C]CCAGGAAGCAGAGGT | 899 |
rs575524437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2451199 | TTCAGAGGTCAGGTC[A/G]TGACGAGAGAAACAG | 899 |
rs575543113 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2448611 | AAGAGATAGGGTCTT[G/T]CTTTGTTGCCCAGGG | 899 |
rs575565260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2454825 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 899 |
rs575579611 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2449591 | GTGAGATACAGCACG[C/G]CTCCTACCTTCAGTG | 899 |
rs575582176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443429 | GTGGAAAGGCCACTG[A/G]CATTTCATTATATAT | 899 |
rs575865727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443904 | CCTGTGACAGGGCGG[C/T]ATAGAGTTCCCTTAT | 899 |
rs575885240 | snp | C/T | 3.34627e-05 | 0.00409026 | intron-variant | CCNF | GRCh38.p7 | 16:2435758 | TGTAGTAGTTCATAA[C/T]GTTTGTGGCATAAAA | 899 |
rs575954456 | in-del | -/CCTGGC | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2454434 | TACTCCAGGAGGGGG[-/CCTGGC]CCTGGCCCTGTGCTC | 899 |
rs575997317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446615 | AGTGCTTTCCAGACC[A/G]ACTCCTCTGTAGAGC | 899 |
rs576017988 | snp | A/G | 1.97221e-05 | 0.00314017 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437300 | TTCACGAGAGCCTCA[A/G]GGCAGAGTGCCAGCT | 899 |
rs576018409 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2436844 | TGGAGGGAGGGTGGG[A/T]CATGAAGCGTCGCGG | 899 |
rs576026186 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456906 | GAAGTCATGTTTACA[A/G]TGTCGTCCCCCAAGT | 899 |
rs576063020 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2432626 | ACAAAACACATTTCC[A/G]TCCTGCCTGCCCCCT | 899 |
rs576092734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446214 | CCAAAGTGTGGCCTC[A/G]CTCTGGCAGGCACAG | 899 |
rs576137094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433137 | TGCCAGTCTGTGTCT[A/C]ACGGCCTGATTCAGC | 899 |
rs576257930 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428029 | GGTAACAGTGACAAA[A/G]TAGGAAACAGTAACC | 899 |
rs576262298 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2450645 | TCTCCCTGACCCGTG[C/G]TAACTTGTGCGTGTT | 899 |
rs576382813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2430820 | CGGCAGCTTTTTCCC[C/T]TTCCTGCCTGTCATG | 899 |
rs576452427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438466 | CCAAAATGGTGAAAC[C/T]ACGTCTTTACTAAAA | 899 |
rs576466187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2439071 | GGGAGACTGAGGTGG[A/G]TGGATCACCTGAGGC | 899 |
rs576842522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436274 | TGCCCTGTAACACAG[A/G]GCCAGGCTTCTAAAC | 899 |
rs576843566 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454487 | CCCGCTTCTCAGAGG[C/T]CCCCCACAGCCCCAT | 899 |
rs576966803 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458502 | TGATCCGCCCACTTC[A/G]GTCTCCCAAAGTGCT | 899 |
rs577025745 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2458023 | CTGCTGTGGGGGCCC[A/G]TGGGAGGGAGGCAGA | 899 |
rs577343138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452472 | CCAACCCTGGCCACC[A/G]AAAGCTGTTTCTGGG | 899 |
rs577375583 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2433511 | TCCCAGGTACCCGCC[A/G]CCCTCAGAACAAACC | 899 |
rs577401176 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428955 | AGCGCCACGTCGAGG[A/C]TGTCCCAGGCTGGAT | 899 |
rs577406404 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CCNF | GRCh38.p7 | 16:2442450 | ATATAATATATAATA[A/T]TATATAATATAATAT | 899 |
rs577583989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447348 | CCAGCACTTTGGGAG[G/T]CTGATGTGGGCGGAT | 899 |
rs577619769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2447915 | CAGGTGTAGTCCCTG[C/T]GCCTCTTGTCCTCTT | 899 |
rs577655516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444416 | ACCATTCTCCTGCCT[C/T]AGCCTCCTCAGGAGC | 899 |
rs577687991 | snp | C/T | 6.18793e-05 | 0.005562 | intron-variant | CCNF | GRCh38.p7 | 16:2449140 | GCCACGGTTGCACCA[C/T]GTCGCCATCTGCGCT | 899 |
rs577808262 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2439158 | CAAAAATTAGCCGGG[A/C]ATGATGGTGGGCTCC | 899 |
rs577862334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438591 | AGGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC | 899 |
rs577942156 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | CCNF | GRCh38.p7 | 16:2441077 | CTTTACTAAAAATAC[-/A]AAAAAAATTAGCTGG | 899 |
rs577972552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445262 | TCGAAGGATGTGGGG[C/T]CTGCTTTGGGGCTGG | 899 |
rs577979025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450529 | AAAAAAAAAAAAGTT[A/C]CAGTAGTTTCTTATC | 899 |
rs578112211 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2438359 | GAGAACAGCAGAGCA[A/G]ATCTCAAGGAGGCAT | 899 |
rs578210266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432452 | TTGGTGCTTAAAGTG[A/T]TCACCTGTGCTCCAG | 899 |
rs578244042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2431763 | AAGACATTCTGATTA[C/T]AGAAATTCCTACTGC | 899 |
rs745443529 | snp | A/G | 1.72988e-05 | 0.00294093 | missense | CCNF | GRCh38.p7 | 16:2455547 | ACCAGGAGAGTGAGG[A/G]CGAGAAGGAGGGCGA | 899 |
rs745445848 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2448240 | TGATAGAGCTGTCAC[A/G]TGACAGGCAAATCTC | 899 |
rs745520562 | snp | A/G | 0.000115349 | 0.00759349 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443759 | GGCTGTCAGTAAACA[A/G]CAAGTCTTCTCCGTG | 899 |
rs745629009 | snp | A/G | 4.94507e-05 | 0.00497221 | intron-variant | CCNF | GRCh38.p7 | 16:2431105 | TTTTTCATCTTATCA[A/G]GGCTTCTGTCTTTTT | 899 |
rs745649290 | snp | C/T | 3.86458e-05 | 0.00439561 | intron-variant | CCNF | GRCh38.p7 | 16:2449167 | CGCTGGTGCGCTACG[C/T]GTGCAGCATCGGCGT | 899 |
rs745709422 | snp | A/G | 1.658e-05 | 0.00287919 | intron-variant | CCNF | GRCh38.p7 | 16:2453374 | CGGGCCTCACCCTCG[A/G]GGCCTCTGCACCCCC | 899 |
rs745717157 | snp | A/G | 1.75823e-05 | 0.00296493 | intron-variant | CCNF | GRCh38.p7 | 16:2437115 | CCTGGGCTCTGTCCT[A/G]TCTGTCCCCGCAGTG | 899 |
rs745725260 | snp | C/T | 2.07114e-05 | 0.00321796 | intron-variant | CCNF | GRCh38.p7 | 16:2449105 | CTGTCTCTGCTGTGC[C/T]CAAAGCCATGGAGCA | 899 |
rs745774088 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2455706 | GCCAGCTCCTGCCCC[A/G]CCGGGGAGTGTGTCC | 899 |
rs745778639 | snp | C/T | 1.70673e-05 | 0.00292119 | intron-variant | CCNF | GRCh38.p7 | 16:2430970 | CCTTTACATAATCTT[C/T]GTTTGGGACAAGAAG | 899 |
rs745821656 | snp | C/T | 1.64942e-05 | 0.00287173 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2438071 | TCCTTTTTTTAAAGA[C/T]TCACAAAGCATCCAT | 899 |
rs745832343 | snp | C/T | 1.6543e-05 | 0.00287597 | intron-variant | CCNF | GRCh38.p7 | 16:2453318 | GGAAGAGGTGCCTCC[C/T]TCCCGCCACCTGGGC | 899 |
rs745850082 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454985 | GACTCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 899 |
rs745887382 | snp | C/T | 1.67024e-05 | 0.0028898 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456730 | CTGGTCCGCACCAGC[C/T]GGGAGCCAGGGAAGG | 899 |
rs745923174 | snp | A/G | 2.24283e-05 | 0.00334868 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437319 | AGAGTGCCAGCTGCA[A/G]AGGGTGAGTCTGGGC | 899 |
rs745923617 | in-del | -/A | 1.66921e-05 | 0.00288891 | utr-variant-5-prime, frameshift-variant | CCNF | GRCh38.p7 | 16:2439773 | CTGGGCGATGCCTCC[-/A]ACAGCTTCCGAAAAC | 899 |
rs745932967 | snp | C/T | 0.000231222 | 0.0107498 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445555 | GTGGACCGGTACCTG[C/T]GGAGGAGGCTGGTGC | 899 |
rs745988003 | in-del | -/AG | 1.69622e-05 | 0.00291219 | intron-variant | CCNF | GRCh38.p7 | 16:2431009 | CATCTTTTGTGGCAC[-/AG]GGAATAGTAACCATT | 899 |
rs745989180 | snp | A/T | 1.65732e-05 | 0.00287859 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445504 | GCCACCATGAAGGAC[A/T]TCACAAGCCTGTGCC | 899 |
rs746002124 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2432875 | ACAGGAGACCCTACA[C/T]CTGCCTCTCGTCCTC | 899 |
rs746127170 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452368 | GTGCCCGGACCCTGT[A/G]CCTTCTGGGCAAGGA | 899 |
rs746151719 | snp | C/T | 3.30918e-05 | 0.00406753 | intron-variant | CCNF | GRCh38.p7 | 16:2433107 | TCAGTCTTCTCCTGC[C/T]TTGGCCTCCCTATGT | 899 |
rs746181188 | snp | A/G | 6.67557e-05 | 0.00577697 | intron-variant | CCNF | GRCh38.p7 | 16:2453587 | TGCTGGCATCCTCGT[A/G]CCGGCCCAGTTCCCT | 899 |
rs746205147 | snp | G/T | 6.31599e-05 | 0.00561925 | intron-variant | CCNF | GRCh38.p7 | 16:2432957 | GGCCCCCGTTGTTCT[G/T]CAGGTACACTCCCAG | 899 |
rs746303419 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2439197 | CAGCTACTCAGGAGG[C/G]TGAGGCAGGAGAATT | 899 |
rs746327360 | snp | G/T | 2.19701e-05 | 0.00331429 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457021 | CTTGTGAGGCTGTAA[G/T]TGTGTCAGCACATTT | 899 |
rs746327714 | snp | G/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428067 | ACAAAAGTGAGATAA[G/T]GGGATAATAAATCTG | 899 |
rs746336128 | snp | C/T | 1.6764e-05 | 0.00289512 | utr-variant-5-prime, stop-gained | CCNF | GRCh38.p7 | 16:2439764 | GTGTCAGATCCTGGG[C/T]GATGCCTCCACAGCT | 899 |
rs746374120 | snp | A/G | 1.65059e-05 | 0.00287275 | intron-variant | CCNF | GRCh38.p7 | 16:2448983 | GGAAGATTCGAGTAA[A/G]CAGCGGTTCCATTTT | 899 |
rs746379136 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2440538 | GCTTGAACCCGGGAG[G/T]CAGAGGTTGCAGTAC | 899 |
rs746391273 | snp | A/G | 0.000210674 | 0.0102612 | intron-variant | CCNF | GRCh38.p7 | 16:2439501 | GAGTTATGCTGGACA[A/G]AGGCGTAGTTGATGC | 899 |
rs746435562 | snp | A/C | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444391 | TGCAAGCTCCACCTC[A/C]CGGGTTCACACCATT | 899 |
rs746526519 | snp | C/G | 1.64838e-05 | 0.00287083 | missense | CCNF | GRCh38.p7 | 16:2448886 | ATCCTGACCATCCGG[C/G]AGGCCGTATGGCTCA | 899 |
rs746621546 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2448038 | GGGCCGCTGGAGCAG[C/T]GTGTTCCCTGATAGT | 899 |
rs746644206 | snp | C/G | 1.71852e-05 | 0.00293127 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437138 | CCGCAGTGTCTGTGT[C/G]TGATGAGGCCCGCGC | 899 |
rs746698931 | snp | C/G | 2.00178e-05 | 0.00316362 | intron-variant | CCNF | GRCh38.p7 | 16:2455616 | ACACAGAGGGTGGCT[C/G]TCACCGAGGGCCTCT | 899 |
rs746724487 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2432409 | ATGGACCCCAGGGGG[A/T]GCTGAATTTCCAATG | 899 |
rs746915605 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454148 | AAGGGCAGGCACTGG[A/G]TGGCTGGGTCTTTCC | 899 |
rs746961242 | snp | C/T | 3.29451e-05 | 0.00405851 | intron-variant | CCNF | GRCh38.p7 | 16:2435902 | CCACCTGCATGTTGG[C/T]GCTTCAGATAAGTGT | 899 |
rs746963376 | snp | C/T | 1.88535e-05 | 0.00307024 | intron-variant | CCNF | GRCh38.p7 | 16:2449174 | GCGCTACGCGTGCAG[C/T]ATCGGCGTGAACATC | 899 |
rs746984895 | snp | C/G | 1.65312e-05 | 0.00287495 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453469 | AGACAGCCCCGACCC[C/G]CCGACTTTCCTCAGC | 899 |
rs747010806 | snp | C/G/T | 4.9442e-05 | 0.00497182 | intron-variant | CCNF | GRCh38.p7 | 16:2431113 | CTTATCAAGGCTTCT[C/G/T]TCTTTTTTTCCTTCA | 899 |
rs747014776 | snp | A/C | 1.65649e-05 | 0.00287788 | intron-variant | CCNF | GRCh38.p7 | 16:2453391 | GCCTCTGCACCCCCT[A/C]ACTCTAGCTTCCCCT | 899 |
rs747048126 | snp | A/G | 0.000115598 | 0.0076017 | synonymous-codon, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456894 | CCATCAGGCCAGGAA[A/G]TCATGTTTACAGTGT | 899 |
rs747062018 | snp | C/T | 5.09714e-05 | 0.00504808 | intron-variant | CCNF | GRCh38.p7 | 16:2431000 | GCATAGTTCCATCTT[C/T]TGTGGCACAGGGAAT | 899 |
rs747066355 | snp | C/T | 6.23811e-05 | 0.0055845 | intron-variant | CCNF | GRCh38.p7 | 16:2439325 | AAAAGAATAAGGGAA[C/T]AATGAACTCTGCTGG | 899 |
rs747120382 | snp | G/T | 0.000166118 | 0.00911217 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456813 | CGTGGACGGTGGCTT[G/T]GGGGCCCTGCCCCAA | 899 |
rs747143311 | in-del | -/CCCTCCATT | 1.65877e-05 | 0.00287986 | intron-variant | CCNF | GRCh38.p7 | 16:2449787 | TCCATCCCCTCCGTC[-/CCCTCCATT]CCCTCCATCCCCTCC | 899 |
rs747155122 | snp | G/T | 1.80455e-05 | 0.00300373 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445652 | TGGCCCAGCTGGCAG[G/T]GACGTGCTGGCCTTT | 899 |
rs747158415 | snp | G/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445127 | CTTCTCCCGCTCCCT[G/T]CACGCCCCGAGGGTC | 899 |
rs747162065 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2430052 | AGGAATATTTTATGG[A/T]GAGGTCTATAGAATC | 899 |
rs747219952 | snp | A/G | 1.66779e-05 | 0.00288768 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456748 | GAGCCAGGGAAGGAC[A/G]TCACGACCTCAGGGT | 899 |
rs747247974 | snp | C/G | 8.24124e-05 | 0.00641868 | intron-variant | CCNF | GRCh38.p7 | 16:2431107 | TTTCATCTTATCAAG[C/G]CTTCTGTCTTTTTTT | 899 |
rs747267245 | snp | A/T | 1.65274e-05 | 0.00287462 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445561 | CGGTACCTGCGGAGG[A/T]GGCTGGTGCCGCGGT | 899 |
rs747267442 | in-del | -/TCCCCTCCG | | | intron-variant | CCNF | GRCh38.p7 | 16:2449776 | CCTCCGTCCCCTCCA[-/TCCCCTCCG]TCCCCTCCGTCCCCT | 899 |
rs747387799 | in-del | -/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2452804 | ATCGGACAAGTGGCC[-/T]TCTGTGTCTAGGTGA | 899 |
rs747471774 | snp | A/G | 3.32116e-05 | 0.00407488 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443607 | ATGGAAAACTGCAAC[A/G]TGGCTGCTGTCTCAC | 899 |
rs747480031 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2438236 | CAAAACAAAAGGCAA[C/G]CCTTGCCCAGAAAGG | 899 |
rs747519392 | in-del | -/C | 1.64987e-05 | 0.00287212 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443636 | CGCTCATGTTTGTCT[-/C]TTTCTTCCTCAGCTG | 899 |
rs747523513 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2453040 | GGGTCTTTACCTAGA[C/G]AGGAATTGCTAGGTC | 899 |
rs747545982 | snp | C/T | 6.28042e-05 | 0.00560341 | intron-variant | CCNF | GRCh38.p7 | 16:2455344 | TGGAGGGCCTGGCCT[C/T]CCAGCGCCGCCGTCC | 899 |
rs747600227 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2448455 | TCTGTCACCCAGGTT[A/G]GAATGCAGTGGTGTA | 899 |
rs747640945 | snp | C/T | 1.94071e-05 | 0.00311499 | intron-variant | CCNF | GRCh38.p7 | 16:2449070 | CTGCTGTGGGAGGGC[C/T]TCATGGACTCAGAGA | 899 |
rs747677407 | snp | A/C | 1.66799e-05 | 0.00288785 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439775 | TGGGCGATGCCTCCA[A/C]AGCTTCCGAAAACTC | 899 |
rs747695958 | snp | A/G | 1.65228e-05 | 0.00287422 | missense | CCNF | GRCh38.p7 | 16:2453269 | CCGCCGTGAAGCAGC[A/G]GTTTGAGGACAAGCG | 899 |
rs747820370 | snp | A/G | 3.31603e-05 | 0.00407174 | intron-variant | CCNF | GRCh38.p7 | 16:2453194 | ACATGTCCACTCCAC[A/G]TGACTCTGTTTCCAG | 899 |
rs747829079 | snp | A/G | 1.72299e-05 | 0.00293508 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456620 | GCTGCCAGGAATCCA[A/G]TGATGAGGAGGCTTG | 899 |
rs747867431 | snp | A/G | 6.59141e-05 | 0.00574045 | intron-variant | CCNF | GRCh38.p7 | 16:2449929 | TGGTGAGTTTTGGCC[A/G]GGCGCAGAGGCTCAT | 899 |
rs747998802 | in-del | -/ATTT | 0.00013599 | 0.00824478 | intron-variant | CCNF | GRCh38.p7 | 16:2439342 | ATGAACTCTGCTGGG[-/ATTT]ATTCTAGGATGAGGA | 899 |
rs748010047 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2446570 | TTTCCTAAACCAGCT[A/G]TCCCCAGCATGGTCT | 899 |
rs748030793 | snp | A/G | 2.44597e-05 | 0.00349704 | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456516 | GCTTGGGTGTGACAT[A/G]ACTTCCCTCCCCACC | 899 |
rs748056817 | snp | A/G | 3.54912e-05 | 0.0042124 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445407 | TGAAATCGCAGACAG[A/G]GACACATGGAGAACG | 899 |
rs748099932 | snp | C/T | | | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447801 | CCCCACCTCTGCTCT[C/T]AGAGGTGCCCTGCCC | 899 |
rs748118739 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433139 | CCAGTCTGTGTCTCA[C/T]GGCCTGATTCAGCAA | 899 |
rs748129007 | snp | A/G | 3.334e-05 | 0.00408276 | missense | CCNF | GRCh38.p7 | 16:2449282 | GTCCCGGCTGTCTAG[A/G]TCCCCACTGTGGTGG | 899 |
rs748191075 | snp | A/C | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431226 | TGAGTCTCCCCGAAG[A/C]TGTGCTCTTTCACAT | 899 |
rs748224007 | snp | A/G | 3.30704e-05 | 0.00406622 | missense | CCNF | GRCh38.p7 | 16:2453473 | AGCCCCGACCCCCCG[A/G]CTTTCCTCAGCACAG | 899 |
rs748232057 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441126 | AGAGTCCCAGCTACG[C/T]GGGAGGCTGAGGCAG | 899 |
rs748255635 | snp | C/G | 1.65594e-05 | 0.0028774 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453532 | CTCGGGGCGGAGAAC[C/G]AAACGGTTAGTTACC | 899 |
rs748281612 | snp | C/G | 5.71772e-05 | 0.00534652 | intron-variant | CCNF | GRCh38.p7 | 16:2439482 | GCCTGCTCTGGGTCG[C/G]GGGGAGTTATGCTGG | 899 |
rs748315822 | snp | C/G | 1.64751e-05 | 0.00287007 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431132 | TTTTTTCCTTCAGTG[C/G]TCCACTGTAGGTGTG | 899 |
rs748334670 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448855 | TTCTCGGCGTTGCAG[A/G]TTTATCAGTAAAGAG | 899 |
rs748356160 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2430003 | ACTGTGGTTTCAGCT[A/G]TTATCATAGTATCTG | 899 |
rs748419408 | snp | C/T | 2.58068e-05 | 0.00359204 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2439379 | GCAGCAGCAGGCCCA[C/T]GACCTGTTTGAGGAG | 899 |
rs748498211 | snp | C/T | 3.30753e-05 | 0.00406652 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445565 | ACCTGCGGAGGAGGC[C/T]GGTGCCGCGGTACAG | 899 |
rs748529790 | snp | C/T | 3.7748e-05 | 0.00434426 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445667 | GGACGTGCTGGCCTT[C/T]CCCGGGTTCAGGGTC | 899 |
rs748608463 | in-del | -/C | 1.65427e-05 | 0.00287595 | frameshift-variant | CCNF | GRCh38.p7 | 16:2453465 | ACAAGACAGCCCCGA[-/C]CCCCCCGACTTTCCT | 899 |
rs748610423 | snp | C/T | 1.65277e-05 | 0.00287464 | intron-variant | CCNF | GRCh38.p7 | 16:2435891 | AAGTCCTCACCCCAC[C/T]TGCATGTTGGCGCTT | 899 |
rs748633093 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2450904 | CAGCTGCTGGGATAG[A/G]GCTATCCTCTGTCTC | 899 |
rs748678831 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2433124 | TGGCCTCCCTATGTG[A/C]CAGTCTGTGTCTCAC | 899 |
rs748686645 | snp | A/C/G | 5.17856e-05 | 0.00508828 | synonymous-codon, missense | CCNF | GRCh38.p7 | 16:2455539 | TGAAGGCGACCAGGA[A/C/G]AGTGAGGGCGAGAAG | 899 |
rs748692628 | in-del | -/TTGT | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445727 | TGGTTTTGTTTTGTG[-/TTGT]TTTTTTTTTTTTCCC | 899 |
rs748739816 | snp | C/T | 1.81674e-05 | 0.00301387 | missense | CCNF | GRCh38.p7 | 16:2455451 | TTACCACCCCCACTG[C/T]GGAGCTGTCCAGCCA | 899 |
rs748823835 | snp | A/G | 1.65493e-05 | 0.00287652 | intron-variant | CCNF | GRCh38.p7 | 16:2435799 | CTTTATGTTCTTAAT[A/G]TTTCAGGGCTGCTGA | 899 |
rs748848689 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2455328 | GTGTTAGAGGCAGGT[G/T]TGGAGGGCCTGGCCT | 899 |
rs748853125 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2436237 | GGCCATCCTCTTAGA[A/T]CTCTCGAGACAGAGT | 899 |
rs748870932 | snp | C/T | 0.00123089 | 0.0247776 | intron-variant | CCNF | GRCh38.p7 | 16:2449160 | CCATCTGCGCTGGTG[C/T]GCTACGCGTGCAGCA | 899 |
rs748912237 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2450670 | CGTGTTGTCAAGTTG[C/T]CATCTAGCTCAGGCA | 899 |
rs748943310 | snp | C/T | | | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437249 | TCTTCATCCGCCCTC[C/T]GTGGTCGGTGAGCGG | 899 |
rs748970301 | snp | A/G | 1.65241e-05 | 0.00287433 | missense | CCNF | GRCh38.p7 | 16:2453290 | AGGACAAGCGCTATG[A/G]AGAAATCAGCCAGGA | 899 |
rs748971721 | in-del | -/CTC | | | intron-variant | CCNF | GRCh38.p7 | 16:2454034 | CACCCGCCTGGAGAA[-/CTC]CTACTGATTCCACAA | 899 |
rs749000412 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2448747 | TCACCAAAGCCCAAC[A/G]CCATGGCTCCCTCCC | 899 |
rs749005310 | snp | A/C | 8.85897e-05 | 0.00665485 | intron-variant | CCNF | GRCh38.p7 | 16:2429536 | GGTTTCTGCCCCACA[A/C]CCCTTCTGCCTGCCC | 899 |
rs749156038 | snp | C/T | 3.30961e-05 | 0.0040678 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453222 | CAGCTTCCATGATGA[C/T]GCCCCCAAGGACTAC | 899 |
rs749212697 | snp | C/T | 1.9197e-05 | 0.00309808 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437295 | CGTGGTTCACGAGAG[C/T]CTCAGGGCAGAGTGC | 899 |
rs749225418 | snp | C/T | | | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2431254 | CATCCTGAAATGGCT[C/T]TCTGTAGAGGACATC | 899 |
rs749253539 | snp | A/G | 1.6557e-05 | 0.00287719 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437218 | CTGAATGTGGGTGCC[A/G]CACCTTTCATCTGGC | 899 |
rs749255027 | in-del | -/TT | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445725 | TTGGTTTTGTTTTGT[-/TT]GTTGTTTTTTTTTTT | 899 |
rs749255669 | snp | A/G | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445136 | CTCCCTGCACGCCCC[A/G]AGGGTCAGGGTTCAT | 899 |
rs749265969 | snp | G/T | 1.65485e-05 | 0.00287645 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445496 | TGGAAGTTGCCACCA[G/T]GAAGGACTTCACAAG | 899 |
rs749266540 | snp | A/C/T | 1.65348e-05 | 0.00287526 | missense | CCNF | GRCh38.p7 | 16:2453467 | CAAGACAGCCCCGAC[A/C/T]CCCCGACTTTCCTCA | 899 |
rs749295733 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459190 | TTTGTGCCCTCCTTC[C/T]CCTCTGCGATGGCAC | 899 |
rs749297488 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438189 | GCCGAGATCCTGGAA[C/T]TGAAAAGCAGCAGAA | 899 |
rs749366538 | snp | A/C/T | 6.7731e-05 | 0.00581907 | missense | CCNF | GRCh38.p7 | 16:2449385 | AGCTCTCCCTGCTGC[A/C/T]CACCAGCCTGTCCGC | 899 |
rs749429314 | snp | C/T | 2.35502e-05 | 0.00343141 | intron-variant | CCNF | GRCh38.p7 | 16:2432948 | CCCAGCCCCGGCCCC[C/T]GTTGTTCTGCAGGTA | 899 |
rs749502766 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2439673 | AAGTTAGCGTAGTGT[C/T]GGCCCTTCTGGGTCT | 899 |
rs749504073 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441074 | CCGTCTTTACTAAAA[A/T]TACAAAAAAATTAGC | 899 |
rs749525736 | snp | A/G | 1.71499e-05 | 0.00292825 | intron-variant | CCNF | GRCh38.p7 | 16:2439741 | GCTCGGTGATCTCCC[A/G]TTGACAGGTGTCAGA | 899 |
rs749536864 | snp | C/T | 1.64735e-05 | 0.00286993 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431241 | ATGTGCTCTTTCACA[C/T]CCTGAAATGGCTTTC | 899 |
rs749544406 | snp | A/T | 1.65693e-05 | 0.00287826 | intron-variant | CCNF | GRCh38.p7 | 16:2453541 | GAGAACCAAACGGTT[A/T]GTTACCCTGCGTTCT | 899 |
rs749553041 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454095 | CTGCTGGCCCTGCGC[C/T]GTGACCCCTCAGCAC | 899 |
rs749597738 | snp | A/C | 3.30606e-05 | 0.00406561 | missense | CCNF | GRCh38.p7 | 16:2453478 | CGACCCCCCGACTTT[A/C]CTCAGCACAGGGGAG | 899 |
rs749608336 | snp | A/G | 2.10042e-05 | 0.00324063 | missense, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457013 | ACCTGGGCCTTGTGA[A/G]GCTGTAAGTGTGTCA | 899 |
rs749710568 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448873 | TATCAGTAAAGAGAT[C/T]CTGACCATCCGGGAG | 899 |
rs749711716 | in-del | -/G | 2.80249e-05 | 0.00374322 | intron-variant | CCNF | GRCh38.p7 | 16:2455366 | CCGCCGTCCATGACT[-/G]GGTCTCCTGGGCTCT | 899 |
rs749735279 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428173 | CCGCTTCCTGATTCC[A/G]GGACAGGGAATATTC | 899 |
rs749778424 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B, splice-donor-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458809 | GGGCAATGATACCTA[C/G]CTCACAGGGGTGTTG | 899 |
rs749786542 | snp | A/C/G | 3.29545e-05 | 0.00405911 | synonymous-codon, missense | CCNF | GRCh38.p7 | 16:2449913 | GAGCCTCCATAAGAA[A/C/G]TGGTGAGTTTTGGCC | 899 |
rs749872028 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440153 | TGTCCCATAGGTAGA[A/G]CTGATCTTGACAACA | 899 |
rs749877657 | snp | A/G | 5.60973e-05 | 0.0052958 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445374 | CCAGCTTATTTGGTC[A/G]GGCCCAACAGGTGGG | 899 |
rs749899048 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2431432 | GCCTTAATCCTAGCA[C/T]TTTGGGAGGCCGAAG | 899 |
rs749925611 | in-del | -/AGG | 3.29462e-05 | 0.00405857 | cds-indel | CCNF | GRCh38.p7 | 16:2431183 | ACAAAGCGAAGAATA[-/AGG]AGGAGGCCCCGAAAC | 899 |
rs749968577 | in-del | -/TATATATATATATATATATA | | | intron-variant | CCNF | GRCh38.p7 | 16:2441938 | ATGATATTAGCAAAT[-/TATATATATATATATATATA]TATATATATATATAT | 899 |
rs749992896 | snp | C/T | 8.36603e-05 | 0.00646708 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443837 | TTCTAATCAGAGCGG[C/T]GCGGAAGCCAGCCTC | 899 |
rs750046213 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2450451 | GGGAGGCAGAGGTTG[C/T]GGTGAGCCGAGATTG | 899 |
rs750109390 | snp | C/T | 1.65416e-05 | 0.00287586 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453511 | CCACGCCTTCCTCAG[C/T]TCTCCCTCGGGGCGG | 899 |
rs750205581 | in-del | -/AG | | | intron-variant | CCNF | GRCh38.p7 | 16:2451178 | GGGAGAGGGCAGGAC[-/AG]AGAGTTCAGAGGTCA | 899 |
rs750242321 | snp | C/G/T | 4.9608e-05 | 0.00498015 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453463 | GACACAAGACAGCCC[C/G/T]GACCCCCCGACTTTC | 899 |
rs750242322 | snp | A/G | 1.73108e-05 | 0.00294195 | synonymous-codon, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456969 | GAAGCGGATAAACCT[A/G]TGCATACACAGTGAG | 899 |
rs750278031 | snp | A/C | 1.64836e-05 | 0.0028708 | intron-variant | CCNF | GRCh38.p7 | 16:2438170 | TGTGTTCGATACATC[A/C]CTAGCCGAGATCCTG | 899 |
rs750311164 | snp | C/T | 1.65477e-05 | 0.00287638 | intron-variant | CCNF | GRCh38.p7 | 16:2448839 | TCCACCCTGAGACCC[C/T]TTCTCGGCGTTGCAG | 899 |
rs750328927 | snp | A/C | 0.000395335 | 0.0140539 | missense | CCNF | GRCh38.p7 | 16:2449877 | CGGATTCTCCTATGA[A/C]GACCTCATTCCCTGC | 899 |
rs750334630 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438460 | GCCTGGCCAAAATGG[C/T]GAAACCACGTCTTTA | 899 |
rs750364006 | snp | A/G | 1.70664e-05 | 0.00292112 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445622 | TGGTCATCTGCACCC[A/G]GTGAGAAGCCCCCTT | 899 |
rs750425630 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2439230 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 899 |
rs750552435 | snp | C/G | 6.961e-05 | 0.00589917 | missense | CCNF | GRCh38.p7 | 16:2455500 | CAGCTTCCTCGACTG[C/G]AGCCTGGACTGCTGC | 899 |
rs750558888 | snp | A/G/T | 3.54687e-05 | 0.0042111 | intron-variant | CCNF | GRCh38.p7 | 16:2437105 | AAGAGACATCCCTGG[A/G/T]CTCTGTCCTGTCTGT | 899 |
rs750578920 | snp | A/G | | | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447624 | GACGTGGTAGTGGGC[A/G]CCTGTAGTCCCATCT | 899 |
rs750598096 | in-del | -/A | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428748 | CGGGGGAGACTTCCC[-/A]GCGTCAGCTCCGACC | 899 |
rs750622990 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2448657 | GGCTGAGCTGTCCTC[C/G]TGCCTGGGCCTCCCC | 899 |
rs750636970 | snp | C/T | 1.88859e-05 | 0.00307288 | missense | CCNF | GRCh38.p7 | 16:2455412 | AGCGGGAGAACAGCC[C/T]CCAGGAAGACAGAGG | 899 |
rs750670416 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433805 | TGGCCAGGATGGTCT[C/T]GATCTCCTGACCTCC | 899 |
rs750731943 | snp | A/G | 2.05929e-05 | 0.00320874 | intron-variant | CCNF | GRCh38.p7 | 16:2449141 | CCACGGTTGCACCAC[A/G]TCGCCATCTGCGCTG | 899 |
rs750793798 | snp | C/G | 1.78522e-05 | 0.0029876 | intron-variant | CCNF | GRCh38.p7 | 16:2439863 | ACGTGGGGAGCTGGC[C/G]TTTCTCCCTCCAGCC | 899 |
rs750901362 | snp | A/G | 1.88827e-05 | 0.00307262 | intron-variant | CCNF | GRCh38.p7 | 16:2449063 | AGCTTTCCTGCTGTG[A/G]GAGGGCCTCATGGAC | 899 |
rs750937982 | snp | A/C | 3.30486e-05 | 0.00406487 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453258 | AGTCTCTCTGACCGC[A/C]GTGAAGCAGCGGTTT | 899 |
rs750992715 | snp | A/G | 3.34902e-05 | 0.00409194 | intron-variant | CCNF | GRCh38.p7 | 16:2437351 | AGGGGCAGCACCTGC[A/G]AGGCCACCTGCAGGG | 899 |
rs750999801 | snp | C/T | 1.73954e-05 | 0.00294913 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437271 | GGTGAGCGGAAGCTG[C/T]TGCAAGGCCGTGGTT | 899 |
rs751022251 | snp | A/C | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427688 | GGAAACGGGCCCACA[A/C]CCTGGAGGAGCCACT | 899 |
rs751060943 | snp | G/T | 1.67192e-05 | 0.00289125 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456689 | CGCTGGACACCCAGA[G/T]CCCTGCAACCCCTGG | 899 |
rs751114062 | snp | C/T | 1.75959e-05 | 0.00296608 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456606 | CCCAGAACAGCATTG[C/T]TGCCAGGAATCCAGT | 899 |
rs751157426 | snp | C/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428881 | GTGCAAGCTGGGGGT[C/G]AGGGTCGCGGGCCCA | 899 |
rs751203430 | snp | A/G | 1.65463e-05 | 0.00287626 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445480 | CTGATCGACTGGCTG[A/G]TGGAAGTTGCCACCA | 899 |
rs751204175 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458665 | GTCTTTTTGCTACTA[C/T]AAGGGAATTCTGGCC | 899 |
rs751260563 | snp | A/G | 1.67458e-05 | 0.00289355 | missense | CCNF | GRCh38.p7 | 16:2449355 | GAACCCAGCACCTGT[A/G]CAGCTTCCTCTGCGA | 899 |
rs751330256 | snp | A/G | 2.83676e-05 | 0.00376603 | intron-variant | CCNF | GRCh38.p7 | 16:2432929 | TTGGGTGGTGCCTCC[A/G]TCACCCAGCCCCGGC | 899 |
rs751348046 | snp | A/G | 8.27438e-05 | 0.00643157 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453520 | CCTCAGCTCTCCCTC[A/G]GGGCGGAGAACCAAA | 899 |
rs751434920 | snp | G/T | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431214 | ACCTGACCATCTTGA[G/T]TCTCCCCGAAGATGT | 899 |
rs751453171 | snp | A/G | 1.78112e-05 | 0.00298417 | intron-variant | CCNF | GRCh38.p7 | 16:2439724 | GACACAGTTGTACAA[A/G]GGCTCGGTGATCTCC | 899 |
rs751512549 | in-del | -/CTC | 2.85955e-05 | 0.00378113 | intron-variant | CCNF | GRCh38.p7 | 16:2433100 | GAATGGCTCAGTCTT[-/CTC]CTGCCTTGGCCTCCC | 899 |
rs751561244 | snp | A/G | 2.40619e-05 | 0.00346848 | intron-variant | CCNF | GRCh38.p7 | 16:2439464 | AGGACAGATGTGAGT[A/G]GTGCCTGCTCTGGGT | 899 |
rs751633956 | snp | C/T | 1.65288e-05 | 0.00287474 | intron-variant | CCNF | GRCh38.p7 | 16:2448847 | GAGACCCCTTCTCGG[C/T]GTTGCAGGTTTATCA | 899 |
rs751657739 | in-del | -/GTGCTGGGGTGT | 1.65674e-05 | 0.00287809 | intron-variant | CCNF | GRCh38.p7 | 16:2453344 | TGGGCGTCTCATGGG[-/GTGCTGGGGTGT]GGGCGGGCCTCACCC | 899 |
rs751730272 | snp | A/G | 8.0402e-05 | 0.00633992 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456549 | CCTTCCTGCAGTGAC[A/G]GCTCCCAGCGGCATC | 899 |
rs751747031 | snp | C/T | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457412 | GTGTGACCTGGGTAG[C/T]CAGACACCACTTGAG | 899 |
rs751799917 | snp | C/G | 1.76403e-05 | 0.00296982 | intron-variant | CCNF | GRCh38.p7 | 16:2437112 | ATCCCTGGGCTCTGT[C/G]CTGTCTGTCCCCGCA | 899 |
rs751843617 | snp | C/G | 1.82537e-05 | 0.00302101 | intron-variant | CCNF | GRCh38.p7 | 16:2455588 | GGGGCCAGGGTGCAC[C/G]AGAAGGGACATCACA | 899 |
rs751851010 | snp | A/C/T | 4.97173e-05 | 0.00498564 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443816 | GTGAGGCATTCAGGC[A/C/T]GGGGCTTCTAATCAG | 899 |
rs752022632 | snp | C/T | 1.74836e-05 | 0.0029566 | intron-variant | CCNF | GRCh38.p7 | 16:2449197 | TGAACATCATCCGGG[C/T]CAGACCCTGCGCTGG | 899 |
rs752068020 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2453848 | CCCGTGCCTGTCATG[C/G]GCGTCCTGGACTTCT | 899 |
rs752075387 | snp | C/T | 1.65441e-05 | 0.00287607 | stop-gained | CCNF | GRCh38.p7 | 16:2453425 | GTGCTGAGCTACAGC[C/T]AGTTGTGTGCTGCAT | 899 |
rs752173112 | snp | A/T | 1.64972e-05 | 0.00287199 | intron-variant | CCNF | GRCh38.p7 | 16:2431081 | TTCAAGGGTGTGTAT[A/T]TAGAATAATTTTTCA | 899 |
rs752189863 | snp | A/G | 3.31494e-05 | 0.00407107 | intron-variant | CCNF | GRCh38.p7 | 16:2453356 | GGGGTGCTGGGGTGT[A/G]GGCGGGCCTCACCCT | 899 |
rs752251200 | snp | A/C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442643 | AATATTATATAATAT[A/C/T]ATATTATTATATATA | 899 |
rs752351900 | snp | C/G | 1.66535e-05 | 0.00288556 | intron-variant | CCNF | GRCh38.p7 | 16:2437373 | CCTGCAGGGTCCCAG[C/G]ACACAGGAAGACCCC | 899 |
rs752358934 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440151 | GTTGTCCCATAGGTA[A/G]AACTGATCTTGACAA | 899 |
rs752414566 | snp | C/T | 1.67133e-05 | 0.00289074 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456700 | CAGATCCCTGCAACC[C/T]CTGGACCCAAACCCC | 899 |
rs752461904 | in-del | -/TG | 1.84599e-05 | 0.00303803 | intron-variant | CCNF | GRCh38.p7 | 16:2449491 | CTTCCCAGGGATGCC[-/TG]TGTCGGGGAAGGTGC | 899 |
rs752507974 | snp | A/C | 0.00013748 | 0.00828982 | intron-variant, missense | CCNF | GRCh38.p7 | 16:2433050 | GCCGTCTCCAGGGAA[A/C]CTGAAGCTCTTTGAA | 899 |
rs752524830 | snp | C/G | 1.70667e-05 | 0.00292114 | missense | CCNF | GRCh38.p7 | 16:2449417 | TACGCCCCAGCCCGC[C/G]TGGCTGCCGCAGCCC | 899 |
rs752529980 | snp | G/T | 1.6552e-05 | 0.00287676 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445486 | GACTGGCTGGTGGAA[G/T]TTGCCACCATGAAGG | 899 |
rs752539641 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427619 | CAGGAATTTCCCTGA[A/G]CTCCTAACAGTTTAG | 899 |
rs752595287 | snp | A/G | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457658 | CAGAGGCGTTCGTAT[A/G]TGACCCACAGATGGC | 899 |
rs752599744 | snp | A/G | 1.66391e-05 | 0.00288431 | intron-variant | CCNF | GRCh38.p7 | 16:2453576 | GCGCCATACAATGCT[A/G]GCATCCTCGTGCCGG | 899 |
rs752630210 | snp | A/G | 3.29685e-05 | 0.00405995 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448903 | GGCCGTATGGCTCAC[A/G]GACAACACTTACAAG | 899 |
rs752644988 | snp | A/G | 3.42783e-05 | 0.0041398 | intron-variant | CCNF | GRCh38.p7 | 16:2439837 | CGCAGGTGAGGTGCG[A/G]GGCTGGGATGACGTG | 899 |
rs752656253 | in-del | -/TCCACCCT | 9.89903e-05 | 0.00703458 | intron-variant | CCNF | GRCh38.p7 | 16:2449807 | CATCCCCTCCACCCC[-/TCCACCCT]TGGCCTGCTTTCCTC | 899 |
rs752685266 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458575 | CTTGAACCGGAAACC[C/T]AGGGATGGGAGATGC | 899 |
rs752802686 | snp | C/T | 1.76303e-05 | 0.00296898 | intron-variant | CCNF | GRCh38.p7 | 16:2439729 | AGTTGTACAAAGGCT[C/T]GGTGATCTCCCATTG | 899 |
rs752803519 | snp | C/T | 3.33795e-05 | 0.00408517 | intron-variant | CCNF | GRCh38.p7 | 16:2449018 | ATTAATCTTCGTTGT[C/T]GCTGTGCTGGAGGGT | 899 |
rs752823768 | snp | C/T | 7.43895e-05 | 0.0060983 | missense, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456995 | GTGAGGAGGAGGACA[C/T]GAACCTGGGCCTTGT | 899 |
rs752843283 | snp | A/G | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445805 | CGATCTTGGCTCACC[A/G]CAACCTCTGCCTCCC | 899 |
rs752872993 | in-del | -/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2452578 | CTACACTTCCTTTGA[-/T]TGTGTGATTTAACGG | 899 |
rs752932301 | snp | A/C/T | 3.29822e-05 | 0.00406082 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448951 | AATGATGGGCGAGAT[A/C/T]GTCTCCGCCTTGGAA | 899 |
rs752981606 | snp | A/C | 1.6486e-05 | 0.00287102 | intron-variant | CCNF | GRCh38.p7 | 16:2449961 | CCTGTAACCCCAGCA[A/C]TTTGGGAGGCCGAGG | 899 |
rs753000700 | snp | A/G | 1.87711e-05 | 0.00306352 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456568 | CCCAGCGGCATCCTC[A/G]ATGTCACCGTGGTCT | 899 |
rs753110068 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449892 | AGACCTCATTCCCTG[C/T]GTCTTGAGCCTCCAT | 899 |
rs753156594 | snp | C/G | 1.74802e-05 | 0.00295632 | intron-variant | CCNF | GRCh38.p7 | 16:2437122 | TCTGTCCTGTCTGTC[C/G]CCGCAGTGTCTGTGT | 899 |
rs753161623 | snp | A/T | 1.84783e-05 | 0.00303954 | intron-variant | CCNF | GRCh38.p7 | 16:2455598 | TGCACCAGAAGGGAC[A/T]TCACACAGAGGGTGG | 899 |
rs753177031 | in-del | -/TT | | | intron-variant | CCNF | GRCh38.p7 | 16:2431370 | CTGTCAGAACAAAAC[-/TT]TGGCTAAAAAAGAGG | 899 |
rs753206686 | in-del | -/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454429 | ACGGCTACTCCAGGA[-/G]GGGGCCTGGCCCTGG | 899 |
rs753207960 | snp | A/G | 1.6577e-05 | 0.00287893 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443819 | AGGCATTCAGGCCGG[A/G]GCTTCTAATCAGAGC | 899 |
rs753329779 | snp | A/G | 1.65444e-05 | 0.00287609 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453430 | GAGCTACAGCCAGTT[A/G]TGTGCTGCATTAGGA | 899 |
rs753372697 | snp | A/G | 6.66659e-05 | 0.00577309 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439443 | CTCCTCTGGGAAAGC[A/G]ACAGGAGGACAGATG | 899 |
rs753420694 | snp | C/T | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431192 | AGAATAAGGAGGAGG[C/T]CCCGAAACCTGACCA | 899 |
rs753439320 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452546 | AAACAAGATAAATTA[A/G]AAACGTTATTTAGAA | 899 |
rs753451182 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2432260 | GACTCTAGGAGTTAT[A/T]TTCTAGATATTGGAA | 899 |
rs753473829 | snp | A/G | 1.64955e-05 | 0.00287184 | intron-variant | CCNF | GRCh38.p7 | 16:2431096 | ATAGAATAATTTTTC[A/G]TCTTATCAAGGCTTC | 899 |
rs753555251 | snp | C/T | 9.9425e-05 | 0.00705001 | intron-variant | CCNF | GRCh38.p7 | 16:2438027 | GTGGCCCCCGGGCAG[C/T]TCTCTGTGCTGGAAA | 899 |
rs753565485 | snp | A/G | 1.65291e-05 | 0.00287476 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456856 | CTGTCCCTGGACAGT[A/G]ACTCGCACACACAGC | 899 |
rs753618927 | snp | C/T | 1.65872e-05 | 0.00287981 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456789 | CAGCACCGCAAGTCC[C/T]ACAAGCTCCGTGGAC | 899 |
rs753669716 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438580 | CTGGGAAGCGGAGGT[C/T]GCAGTGAGCCGAGAT | 899 |
rs753728750 | in-del | -/G | 1.66863e-05 | 0.0028884 | intron-variant | CCNF | GRCh38.p7 | 16:2453162 | ACTGAAGCTAAAAAT[-/G]GGGGTGGGGGTGCCT | 899 |
rs753737392 | snp | G/T | 3.64279e-05 | 0.00426762 | intron-variant | CCNF | GRCh38.p7 | 16:2449484 | AGTGGCCCTTCCCAG[G/T]GATGCCTGTGTCGGG | 899 |
rs753738860 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427404 | CAGTCCTCGTTTCAG[A/G]TGACTGCTCCCTGTG | 899 |
rs753785529 | snp | A/T | 1.65127e-05 | 0.00287334 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2435838 | ATTTCGAAGCTGCTG[A/T]GAAGCTGGGCATAGC | 899 |
rs753790420 | snp | C/T | 1.75545e-05 | 0.00296259 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455491 | GCTGCTGGGCAGCTT[C/T]CTCGACTGGAGCCTG | 899 |
rs753790591 | snp | A/G | 6.84943e-05 | 0.00585171 | missense | CCNF | GRCh38.p7 | 16:2449426 | GCCCGCCTGGCTGCC[A/G]CAGCCCTGCTCCTGG | 899 |
rs753802130 | snp | C/T | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457527 | TGCATGGGGCACCCA[C/T]TTCCTTCTGGGTGGG | 899 |
rs753913259 | snp | A/G | 1.6486e-05 | 0.00287102 | missense | CCNF | GRCh38.p7 | 16:2455406 | GCAGGAAGCGGGAGA[A/G]CAGCCTCCAGGAAGA | 899 |
rs753932077 | snp | A/T | 2.23396e-05 | 0.00334205 | intron-variant | CCNF | GRCh38.p7 | 16:2433073 | TCTTTGAAAGGTATC[A/T]CTGCACCCTGAGAAT | 899 |
rs753937291 | snp | A/C | 0.000115316 | 0.00759243 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443683 | GTGCAAATGCAAACC[A/C]GCTTGGACTGGAGGT | 899 |
rs753956210 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2436941 | ATGACCCACCTGTTC[C/T]AGACATTAATGAAGT | 899 |
rs754007181 | in-del | -/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452212 | AGATCAGAACTCCCT[-/G]GGGGGTCTCGATGCC | 899 |
rs754177356 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2447852 | CACGCTGGGCTCTCA[C/T]TGGCCACTGACATCT | 899 |
rs754199256 | snp | A/T | 0.000100363 | 0.00708318 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456682 | GCACTGGCGCTGGAC[A/T]CCCAGATCCCTGCAA | 899 |
rs754219533 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2441824 | ACCTGGCCAAAAAAA[A/G]TTAATAATAAATAAA | 899 |
rs754242856 | snp | A/G | 3.29875e-05 | 0.00406112 | missense | CCNF | GRCh38.p7 | 16:2448958 | GGCGAGATCGTCTCC[A/G]CCTTGGAAGGGAAGA | 899 |
rs754274230 | snp | A/G | 1.64893e-05 | 0.0028713 | intron-variant | CCNF | GRCh38.p7 | 16:2449967 | ACCCCAGCACTTTGG[A/G]AGGCCGAGGCGGGCA | 899 |
rs754284159 | snp | A/G | 5.07859e-05 | 0.00503889 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437256 | CCGCCCTCCGTGGTC[A/G]GTGAGCGGAAGCTGC | 899 |
rs754303582 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434238 | TTAAACCCAGCAGGT[A/G]GAGGTTGCAGTGAGC | 899 |
rs754353054 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2430709 | TCTTTATTGAACATT[A/G]TGCACCTTGGTCACG | 899 |
rs754383219 | snp | A/C | 3.4753e-05 | 0.00416837 | intron-variant | CCNF | GRCh38.p7 | 16:2437355 | GCAGCACCTGCGAGG[A/C]CACCTGCAGGGTCCC | 899 |
rs754435611 | snp | C/G | 1.65512e-05 | 0.00287669 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445473 | GTACATTCTGATCGA[C/G]TGGCTGGTGGAAGTT | 899 |
rs754443604 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2451832 | ACCCCAAGGGGCCCC[A/G]GAATTCTGGCTTTCT | 899 |
rs754484514 | snp | C/T | 1.65902e-05 | 0.00288008 | intron-variant | CCNF | GRCh38.p7 | 16:2453190 | CCTCACATGTCCACT[C/T]CACGTGACTCTGTTT | 899 |
rs754607732 | snp | G/T | 5.19827e-05 | 0.00509791 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456616 | CATTGCTGCCAGGAA[G/T]CCAGTGATGAGGAGG | 899 |
rs754634598 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452621 | ACAGTTGTGCTTGTC[A/G]TCACAACAATCAAAT | 899 |
rs754701735 | in-del | -/C | 3.36428e-05 | 0.00410125 | intron-variant | CCNF | GRCh38.p7 | 16:2435921 | TCAGATAAGTGTGAG[-/C]CTTTGGCCCTATGAA | 899 |
rs754757995 | snp | A/G | 0.000162791 | 0.00902049 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445399 | GGTGGGGTTGAAATC[A/G]CAGACAGGGACACAT | 899 |
rs754760067 | snp | A/C/G | 6.70404e-05 | 0.00578935 | missense | CCNF | GRCh38.p7 | 16:2449358 | CCCAGCACCTGTGCA[A/C/G]CTTCCTCTGCGAGCT | 899 |
rs754766175 | snp | A/G | 1.66095e-05 | 0.00288175 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456781 | TCCTCCGTCAGCACC[A/G]CAAGTCCCACAAGCT | 899 |
rs754803917 | snp | C/T | 1.64838e-05 | 0.00287083 | intron-variant | CCNF | GRCh38.p7 | 16:2432938 | GCCTCCATCACCCAG[C/T]CCCGGCCCCCGTTGT | 899 |
rs754833495 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2455180 | GCTTCACACCCAGAC[C/G]TGGGGCCTGAGTTTG | 899 |
rs754886746 | snp | A/G | 1.66879e-05 | 0.00288855 | intron-variant | CCNF | GRCh38.p7 | 16:2449272 | CCCACACCCCGTCCC[A/G]GCTGTCTAGGTCCCC | 899 |
rs754886949 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458346 | ACTCACTGTAACCTC[C/T]GCCTCCCGGATACTC | 899 |
rs754920554 | snp | A/C/T | 3.31061e-05 | 0.00406844 | synonymous-codon, missense | CCNF | GRCh38.p7 | 16:2453524 | AGCTCTCCCTCGGGG[A/C/T]GGAGAACCAAACGGT | 899 |
rs754969037 | snp | C/T | 4.95929e-05 | 0.00497936 | missense | CCNF | GRCh38.p7 | 16:2453471 | ACAGCCCCGACCCCC[C/T]GACTTTCCTCAGCAC | 899 |
rs754982220 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2446499 | TAACTAATGCTGGAT[C/T]CCCTAGTTCCGCCTT | 899 |
rs755002224 | snp | A/G | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457650 | CTCTGTCCCAGAGGC[A/G]TTCGTATGTGACCCA | 899 |
rs755029983 | snp | A/G | 8.26057e-05 | 0.0064262 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456905 | GGAAGTCATGTTTAC[A/G]GTGTCGTCCCCCAAG | 899 |
rs755047457 | snp | A/G/T | 3.58585e-05 | 0.00423417 | missense, stop-gained, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456985 | TGCATACACAGTGAG[A/G/T]AGGAGGACATGAACC | 899 |
rs755065212 | in-del | -/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2452456 | GGGAGCACAGATCGT[-/C]CCAACCCTGGCCACC | 899 |
rs755122360 | snp | C/T | 6.59e-05 | 0.00573983 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449889 | TGAAGACCTCATTCC[C/T]TGCGTCTTGAGCCTC | 899 |
rs755137166 | in-del | -/C | 1.65836e-05 | 0.0028795 | intron-variant | CCNF | GRCh38.p7 | 16:2453385 | CTCGGGGCCTCTGCA[-/C]CCCCTAACTCTAGCT | 899 |
rs755211187 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2441851 | TAAATAAACTCAAGT[C/G]GTTAGAAATTGGAAT | 899 |
rs755228491 | snp | C/G | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444454 | ACAGGTGCCTGCCAC[C/G]ACGCCCAGCTAATTT | 899 |
rs755299106 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2429838 | ACACCAGCGCCTCCT[C/G]GTCGGGGAAAGGGCT | 899 |
rs755321258 | snp | A/G | 1.94558e-05 | 0.0031189 | intron-variant | CCNF | GRCh38.p7 | 16:2449514 | GGAAGGTGCTGACAT[A/G]GGAGGAGGCTGTGGG | 899 |
rs755345423 | snp | A/G | 1.82844e-05 | 0.00302355 | intron-variant | CCNF | GRCh38.p7 | 16:2455591 | GCCAGGGTGCACCAG[A/G]AGGGACATCACACAG | 899 |
rs755360751 | snp | A/C | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429128 | CCACAAACCCCTGCC[A/C]GCCGGCCGGGAAGCG | 899 |
rs755361178 | snp | C/T | 4.95708e-05 | 0.00497825 | intron-variant | CCNF | GRCh38.p7 | 16:2435883 | AAGGCCGTAAGTCCT[C/T]ACCCCACCTGCATGT | 899 |
rs755459282 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2430801 | GGAAAACCGTCCTCA[C/G]CTTCGGCAGCTTTTT | 899 |
rs755574725 | snp | A/G | 8.00432e-05 | 0.00632576 | intron-variant | CCNF | GRCh38.p7 | 16:2449156 | GTCGCCATCTGCGCT[A/G]GTGCGCTACGCGTGC | 899 |
rs755577885 | snp | C/T | 0.000346098 | 0.0131503 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448900 | GGAGGCCGTATGGCT[C/T]ACGGACAACACTTAC | 899 |
rs755625264 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2430574 | ACAATAGAGGGCACA[C/T]TGAGACTCTGCAGAG | 899 |
rs755638356 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458718 | GGTGAGAACCCAAGC[A/G]TTGGAACTGTAGACC | 899 |
rs755661506 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433545 | GAACCACAGCTCAGG[C/T]GGGGATTTTTCTTTT | 899 |
rs755670344 | snp | A/G | 3.2994e-05 | 0.00406152 | intron-variant | CCNF | GRCh38.p7 | 16:2431088 | GTGTGTATATAGAAT[A/G]ATTTTTCATCTTATC | 899 |
rs755721747 | snp | A/C | 9.98004e-05 | 0.0070633 | utr-variant-5-prime, synonymous-codon, intron-variant | CCNF | GRCh38.p7 | 16:2429496 | GATGGGGAGCGGCGG[A/C]GGTGAGTGCGGGGCG | 899 |
rs755746805 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2451412 | GGGGCTGAATTTGTA[C/G]CCGGCCAGCCATCTC | 899 |
rs755777856 | snp | C/T | 9.96396e-05 | 0.00705761 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456780 | CTCCTCCGTCAGCAC[C/T]GCAAGTCCCACAAGC | 899 |
rs755825085 | snp | C/T | 1.67175e-05 | 0.0028911 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456706 | CCTGCAACCCCTGGA[C/T]CCAAACCCCTGGTCC | 899 |
rs755865006 | snp | C/T | 3.32287e-05 | 0.00407593 | intron-variant | CCNF | GRCh38.p7 | 16:2438020 | GGGAGTGGTGGCCCC[C/T]GGGCAGTTCTCTGTG | 899 |
rs755943561 | in-del | -/ACATATATATATATATAT | | | intron-variant | CCNF | GRCh38.p7 | 16:2435664 | TATATGCACACACAC[-/ACATATATATATATATAT]ACATATATATATATA | 899 |
rs755954398 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458542 | GGCATGAGCCACGGC[A/G]CCTGGCCCCCAAATG | 899 |
rs756007066 | snp | G/T | 1.65526e-05 | 0.00287681 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445487 | ACTGGCTGGTGGAAG[G/T]TGCCACCATGAAGGA | 899 |
rs756058100 | snp | A/G | 1.67998e-05 | 0.00289821 | missense | CCNF | GRCh38.p7 | 16:2449369 | TGCAGCTTCCTCTGC[A/G]AGCTCTCCCTGCTGC | 899 |
rs756078572 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2434008 | TCACACAATTCATCC[A/T]TTTAAAGTGTATAAC | 899 |
rs756107653 | snp | C/G | 3.94485e-05 | 0.00444102 | intron-variant, missense | CCNF | GRCh38.p7 | 16:2433051 | CCGTCTCCAGGGAAC[C/G]TGAAGCTCTTTGAAA | 899 |
rs756147458 | snp | C/T | 0.000316363 | 0.0125731 | intron-variant | CCNF | GRCh38.p7 | 16:2453578 | GCCATACAATGCTGG[C/T]ATCCTCGTGCCGGCC | 899 |
rs756177719 | snp | A/C | 0.000100271 | 0.00707992 | intron-variant | CCNF | GRCh38.p7 | 16:2449262 | GCGCTGAGAGCCCAC[A/C]CCCCGTCCCGGCTGT | 899 |
rs756190522 | snp | A/G | 1.65608e-05 | 0.00287752 | missense | CCNF | GRCh38.p7 | 16:2453533 | TCGGGGCGGAGAACC[A/G]AACGGTTAGTTACCC | 899 |
rs756199019 | snp | A/G | 3.05824e-05 | 0.00391028 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457060 | GGATGTGTACTGAGG[A/G]GGCTGGAGGCGAAGG | 899 |
rs756208265 | snp | A/G | 3.51253e-05 | 0.00419063 | intron-variant | CCNF | GRCh38.p7 | 16:2439730 | GTTGTACAAAGGCTC[A/G]GTGATCTCCCATTGA | 899 |
rs756315442 | snp | C/T | 1.90308e-05 | 0.00308464 | synonymous-codon, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456999 | GGAGGAGGACATGAA[C/T]CTGGGCCTTGTGAGG | 899 |
rs756330740 | snp | A/G | 2.96055e-05 | 0.00384732 | intron-variant | CCNF | GRCh38.p7 | 16:2439486 | GCTCTGGGTCGGGGG[A/G]AGTTATGCTGGACAA | 899 |
rs756448731 | snp | A/G | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445910 | TTTTTTTGTATTTTT[A/G]GTAGAGACGGGGTTT | 899 |
rs756499606 | snp | G/T | 1.64855e-05 | 0.00287097 | intron-variant | CCNF | GRCh38.p7 | 16:2449962 | CTGTAACCCCAGCAC[G/T]TTGGGAGGCCGAGGC | 899 |
rs756501762 | snp | A/G | 1.64868e-05 | 0.00287109 | missense | CCNF | GRCh38.p7 | 16:2448865 | TGCAGGTTTATCAGT[A/G]AAGAGATCCTGACCA | 899 |
rs756505843 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2440763 | GGTGTCATAGCACAT[G/T]GTGGTGTTCACGTCC | 899 |
rs756519948 | snp | A/G | 8.27972e-05 | 0.00643364 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437180 | GCCTGAAGGCCTCTC[A/G]CTTCTTCAGTCTCGC | 899 |
rs756568009 | snp | C/T | 1.88745e-05 | 0.00307195 | intron-variant | CCNF | GRCh38.p7 | 16:2455604 | AGAAGGGACATCACA[C/T]AGAGGGTGGCTCTCA | 899 |
rs756652350 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2431411 | AGGCCAGGCACGGTG[G/T]CTCATGCCTTAATCC | 899 |
rs756713242 | in-del | -/CAG | 1.65319e-05 | 0.00287501 | cds-indel | CCNF | GRCh38.p7 | 16:2453481 | CCCCCCGACTTTCCT[-/CAG]CACAGGGGAGATCCA | 899 |
rs756734231 | snp | G/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427959 | AGTTGATTAATCCCT[G/T]CAAGATGCTATGGAA | 899 |
rs756743855 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2429831 | GAGCCAAACACCAGC[G/T]CCTCCTGGTCGGGGA | 899 |
rs756771599 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441404 | CTATCTCAACAAAAA[C/T]ATTGTTTACAAGAAA | 899 |
rs756837670 | snp | C/T | 1.94964e-05 | 0.00312215 | intron-variant | CCNF | GRCh38.p7 | 16:2449165 | TGCGCTGGTGCGCTA[C/T]GCGTGCAGCATCGGC | 899 |
rs756862863 | snp | C/T | 5.10208e-05 | 0.00505053 | intron-variant | CCNF | GRCh38.p7 | 16:2449218 | CCTGCGCTGGGCCTG[C/T]ATGCGGCACTGCACC | 899 |
rs756880726 | snp | C/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428929 | CGGGCAGGGCACGGC[C/T]TCGTCTTAGAAGCGC | 899 |
rs756897881 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2450677 | TCAAGTTGTCATCTA[G/T]CTCAGGCACTGGCAC | 899 |
rs756901012 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458688 | TTCTGGCCACCCTGG[A/G]TGGGGTGTGGTCGGG | 899 |
rs756914411 | snp | C/T | 1.65389e-05 | 0.00287562 | missense | CCNF | GRCh38.p7 | 16:2453450 | CTGCATTAGGAGTGA[C/T]ACAAGACAGCCCCGA | 899 |
rs757001849 | in-del | -/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2435262 | CTCAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAA | 899 |
rs757002386 | snp | A/T | 3.2987e-05 | 0.00406108 | intron-variant | CCNF | GRCh38.p7 | 16:2431102 | TAATTTTTCATCTTA[A/T]CAAGGCTTCTGTCTT | 899 |
rs757014272 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2450435 | AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG | 899 |
rs757049637 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435983 | TGTCCTTGCTCTATC[C/T]GATGGCCTGCCTCCC | 899 |
rs757060245 | snp | A/G | 3.33528e-05 | 0.00408354 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445600 | CAGCTGCTGGGCATC[A/G]CCTGCATGGTCATCT | 899 |
rs757135222 | snp | G/T | 1.65542e-05 | 0.00287695 | intron-variant | CCNF | GRCh38.p7 | 16:2438034 | CCGGGCAGTTCTCTG[G/T]GCTGGAAATCACACT | 899 |
rs757188816 | snp | A/G | 4.95291e-05 | 0.00497615 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445547 | TGGAGTGTGTGGACC[A/G]GTACCTGCGGAGGAG | 899 |
rs757219651 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2446347 | GCCAGAGTTTCCTAC[A/G]CTCTTGGAGTTAGAG | 899 |
rs757281805 | snp | C/T | 3.42548e-05 | 0.00413838 | missense | CCNF | GRCh38.p7 | 16:2449427 | CCCGCCTGGCTGCCG[C/T]AGCCCTGCTCCTGGC | 899 |
rs757283933 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2437032 | CTTTGCACTATGGTG[A/G]GCTTCAGGCATTACA | 899 |
rs757336351 | snp | A/G | 1.91166e-05 | 0.00309159 | missense | CCNF | GRCh38.p7 | 16:2455408 | AGGAAGCGGGAGAAC[A/G]GCCTCCAGGAAGACA | 899 |
rs757482931 | in-del | -/G | 5.59965e-05 | 0.00529104 | intron-variant | CCNF | GRCh38.p7 | 16:2439480 | TGCCTGCTCTGGGTC[-/G]GGGGGGAGTTATGCT | 899 |
rs757493735 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2432676 | CTTTGGGGGTGATAC[C/T]TTTGCAGGGATGTTG | 899 |
rs757581748 | snp | A/G | 1.67801e-05 | 0.00289651 | intron-variant | CCNF | GRCh38.p7 | 16:2449027 | CGTTGTCGCTGTGCT[A/G]GAGGGTGGGGGTGGG | 899 |
rs757639588 | snp | A/G | 1.69712e-05 | 0.00291295 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439749 | ATCTCCCATTGACAG[A/G]TGTCAGATCCTGGGC | 899 |
rs757660294 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2453080 | CTGAGTTTAACCATT[C/T]GGGGAACTGCCAGGT | 899 |
rs757704196 | snp | A/G/T | 3.30514e-05 | 0.00406507 | missense | CCNF | GRCh38.p7 | 16:2453256 | CAAGTCTCTCTGACC[A/G/T]CCGTGAAGCAGCGGT | 899 |
rs757764626 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448961 | GAGATCGTCTCCGCC[C/T]TGGAAGGGAAGATTC | 899 |
rs757836181 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440449 | CATGGTGAAACCATC[A/G]CTACTAAAAATACAA | 899 |
rs757857382 | snp | A/G | 3.30666e-05 | 0.00406598 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437194 | CGCTTCTTCAGTCTC[A/G]CTGAGCGGCTGAATG | 899 |
rs757858857 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2431862 | TTGAGACAGAGTCTC[A/G]CTCTGCCACCCAGGC | 899 |
rs757868114 | snp | G/T | 1.83195e-05 | 0.00302646 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456580 | CTCGATGTCACCGTG[G/T]TCTACCTGAACCCAG | 899 |
rs757883816 | in-del | -/CCC | 2.53174e-05 | 0.00355782 | intron-variant | CCNF | GRCh38.p7 | 16:2432943 | ATCACCCAGCCCCGG[-/CCC]CCCCCGTTGTTCTGC | 899 |
rs757891079 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2453890 | TGCTGCTGTCACTCC[C/T]GGCACTCGAGCTGTG | 899 |
rs757921005 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434256 | GGTTGCAGTGAGCCA[A/G]GATTGCGCCATTGCA | 899 |
rs757943199 | snp | A/G | 1.89824e-05 | 0.00308072 | intron-variant | CCNF | GRCh38.p7 | 16:2455608 | GGGACATCACACAGA[A/G]GGTGGCTCTCACCGA | 899 |
rs757982310 | snp | C/T | 1.85903e-05 | 0.00304874 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445379 | TTATTTGGTCGGGCC[C/T]AACAGGTGGGGTTGA | 899 |
rs758017598 | snp | C/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427651 | CTTTTCCAACAAGGT[C/G]TCACCTTCCTGAAGC | 899 |
rs758077102 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454717 | AAGGCCAGGCCATTC[C/T]ATGCAATCTGCCTGG | 899 |
rs758116753 | snp | A/G | 3.29457e-05 | 0.00405854 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431198 | AGGAGGAGGCCCCGA[A/G]ACCTGACCATCTTGA | 899 |
rs758172510 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458594 | GATGGGAGATGCTCA[C/G]TGAGCTGCTGCTTTT | 899 |
rs758226199 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2447994 | GCCAAGGGACTTGGC[C/G]TCAGTCCAAGGGGAA | 899 |
rs758304617 | snp | A/G | 1.65734e-05 | 0.00287862 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456801 | TCCCACAAGCTCCGT[A/G]GACGGTGGCTTGGGG | 899 |
rs758338026 | snp | C/T | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456871 | GACTCGCACACACAG[C/T]CCTGCCACCATCAGG | 899 |
rs758358995 | snp | C/T | 3.30819e-05 | 0.00406692 | intron-variant | CCNF | GRCh38.p7 | 16:2448844 | CCTGAGACCCCTTCT[C/T]GGCGTTGCAGGTTTA | 899 |
rs758360948 | snp | A/G | 1.66576e-05 | 0.00288592 | intron-variant | CCNF | GRCh38.p7 | 16:2439309 | CAAAAAATAAAAATG[A/G]AAAAGAATAAGGGAA | 899 |
rs758414416 | snp | C/T | 1.76468e-05 | 0.00297037 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445641 | AGAAGCCCCCTTGGC[C/T]CAGCTGGCAGGGACG | 899 |
rs758432533 | in-del | -/TCCCCTCCA | 0.000179179 | 0.00946349 | intron-variant | CCNF | GRCh38.p7 | 16:2449786 | CCTCCATCCCCTCCG[-/TCCCCTCCA]TCCCCTCCACCCCTG | 899 |
rs758432974 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2455654 | CGGCCCTGTGCGAGC[A/G]CTGTGGGAGGAAGAT | 899 |
rs758523853 | snp | A/G | 1.73902e-05 | 0.0029487 | missense | CCNF | GRCh38.p7 | 16:2455502 | GCTTCCTCGACTGGA[A/G]CCTGGACTGCTGCTC | 899 |
rs758532080 | in-del | -/GG | 1.66888e-05 | 0.00288862 | intron-variant | CCNF | GRCh38.p7 | 16:2453167 | AGCTAAAAATGGGGT[-/GG]GGGGGTGCCTCACAT | 899 |
rs758615701 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2446227 | TCGCTCTGGCAGGCA[C/T]AGGCTGGACTGCCCT | 899 |
rs758671258 | snp | C/G | | | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456355 | TCTCCACATTTGTTG[C/G]AGTCATGGCGGGCAG | 899 |
rs758720929 | snp | C/G | 1.64743e-05 | 0.00287 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443710 | AGGTGAGAGCTTCCA[C/G]TGAGATCGTCTGCCA | 899 |
rs758745555 | snp | C/T | 3.76818e-05 | 0.00434045 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455413 | GCGGGAGAACAGCCT[C/T]CAGGAAGACAGAGGC | 899 |
rs758746222 | snp | C/T | 1.81817e-05 | 0.00301504 | intron-variant | CCNF | GRCh38.p7 | 16:2439870 | GAGCTGGCCTTTCTC[C/T]CTCCAGCCTTGGGGC | 899 |
rs758779951 | snp | C/T | 1.65581e-05 | 0.00287728 | intron-variant | CCNF | GRCh38.p7 | 16:2433113 | TTCTCCTGCCTTGGC[C/T]TCCCTATGTGCCAGT | 899 |
rs758799525 | snp | A/G | 1.8897e-05 | 0.00307378 | intron-variant | CCNF | GRCh38.p7 | 16:2449064 | GCTTTCCTGCTGTGG[A/G]AGGGCCTCATGGACT | 899 |
rs758870842 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2452187 | GGCCTCGCTGTCCGG[C/T]TTCCAGGATGAGATC | 899 |
rs758932928 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2452693 | CAGCTGTCACCCTCC[C/T]GTTCCCCCCAACTTC | 899 |
rs758999973 | snp | A/G | 1.66499e-05 | 0.00288525 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456764 | TCACGACCTCAGGGT[A/G]CTCCTCCGTCAGCAC | 899 |
rs759029593 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2433422 | TGAATTCTATCCTAT[A/G]GCGTTTCACTCACTG | 899 |
rs759052794 | snp | A/G | 1.65556e-05 | 0.00287707 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445574 | GGAGGCTGGTGCCGC[A/G]GTACAGGCTCCAGCT | 899 |
rs759091896 | in-del | -/CCCTCCA | 1.76791e-05 | 0.00297308 | intron-variant | CCNF | GRCh38.p7 | 16:2449804 | CTCCATCCCCTCCAC[-/CCCTCCA]CCCTGGCCTGCTTTC | 899 |
rs759163200 | snp | A/G | 1.65042e-05 | 0.0028726 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445531 | TGCCTGCACCTGACC[A/G]TGGAGTGTGTGGACC | 899 |
rs759191535 | snp | A/T | 4.95618e-05 | 0.00497779 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2435814 | GTTTCAGGGCTGCTG[A/T]AAAGGGGAATTTCGA | 899 |
rs759232116 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2434736 | CCCCAAGAAGAAAGC[C/T]TGTCCCCATCAGCAG | 899 |
rs759310695 | snp | A/G | 3.7553e-05 | 0.00433303 | intron-variant, synonymous-codon | CCNF | GRCh38.p7 | 16:2433038 | CCAGGAGCTGTGGCC[A/G]TCTCCAGGGAACCTG | 899 |
rs759316148 | snp | C/T | 0.000160884 | 0.0089675 | intron-variant | CCNF | GRCh38.p7 | 16:2455370 | CGTCCATGACTGGGT[C/T]TCCTGGGCTCTCTCC | 899 |
rs759371495 | snp | A/G | 8.04689e-05 | 0.00634255 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457046 | ACATTTGCCGCAGTG[A/G]ATGTGTACTGAGGGG | 899 |
rs759451741 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428532 | TGGCTGACTCCTGAA[A/G]GACAGCTCAGATGGG | 899 |
rs759457752 | in-del | -/CAT | 3.61945e-05 | 0.00425393 | intron-variant | CCNF | GRCh38.p7 | 16:2449186 | CAGCATCGGCGTGAA[-/CAT]CATCCGGGCCAGACC | 899 |
rs759504925 | snp | C/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427539 | GGCTCCCAAGCTACT[C/T]CACTTTCCCTTCTCT | 899 |
rs759632058 | snp | G/T | 6.61419e-05 | 0.00575036 | missense | CCNF | GRCh38.p7 | 16:2453239 | CCCCCAAGGACTACA[G/T]GCAAGTCTCTCTGAC | 899 |
rs759799328 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433533 | GAACAAACCAAGGAA[C/T]CACAGCTCAGGCGGG | 899 |
rs759830444 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2456228 | CTGCCCTGTGCAAAC[C/T]CCAGGCAGACTGCGG | 899 |
rs759831838 | snp | C/T | 1.88784e-05 | 0.00307227 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445347 | AGGGTAAACCCATGA[C/T]TCCAGAGCTAGCCAG | 899 |
rs759832040 | snp | G/T | 1.66682e-05 | 0.00288684 | missense | CCNF | GRCh38.p7 | 16:2449310 | TGGATTACAAGGAGG[G/T]CCTGCTGACGCTAGT | 899 |
rs759921834 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454215 | CGTTGTGTCGGGAGT[A/G]GGCTCCTGGCAGGAG | 899 |
rs759952513 | snp | A/C | 3.35655e-05 | 0.00409654 | intron-variant | CCNF | GRCh38.p7 | 16:2449246 | ACCAAGGAGCCCCCG[A/C]GCGCTGAGAGCCCAC | 899 |
rs760005983 | snp | C/T | 1.72421e-05 | 0.00293611 | intron-variant | CCNF | GRCh38.p7 | 16:2449204 | CATCCGGGCCAGACC[C/T]TGCGCTGGGCCTGCA | 899 |
rs760054447 | snp | A/C | 1.65438e-05 | 0.00287605 | missense | CCNF | GRCh38.p7 | 16:2453426 | TGCTGAGCTACAGCC[A/C]GTTGTGTGCTGCATT | 899 |
rs760058825 | snp | G/T | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457163 | GGCCACCAAGTTTCT[G/T]TCTCCGCGGGAGTCC | 899 |
rs760059278 | snp | A/C | 1.6534e-05 | 0.00287519 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453496 | CAGCACAGGGGAGAT[A/C]CACGCCTTCCTCAGC | 899 |
rs760061418 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2432398 | CGACACACTTTATGG[A/T]CCCCAGGGGGTGCTG | 899 |
rs760072087 | snp | A/T | 1.64762e-05 | 0.00287016 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431262 | AATGGCTTTCTGTAG[A/T]GGACATCCTGGCCGT | 899 |
rs760107270 | snp | A/G | 0.000314057 | 0.0125272 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456850 | TCAGTGCTGTCCCTG[A/G]ACAGTGACTCGCACA | 899 |
rs760154270 | snp | C/T | 1.6693e-05 | 0.00288898 | intron-variant | CCNF | GRCh38.p7 | 16:2448826 | CCAGGAAGTGGGCTC[C/T]ACCCTGAGACCCCTT | 899 |
rs760181877 | snp | C/T | 1.66785e-05 | 0.00288773 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456941 | CGGAGAGCAGTGTTC[C/T]CCAGCAACAGGTGAA | 899 |
rs760251490 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2440773 | CACATTGTGGTGTTC[A/T]CGTCCAAAAAGCCAG | 899 |
rs760258166 | snp | A/C | 4.27177e-05 | 0.00462137 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2439430 | GACCAGCTCCTACCT[A/C]CTCTGGGAAAGCGAC | 899 |
rs760280974 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | CCNF | GRCh38.p7 | 16:2449861 | AGCTGTGGGACCTCA[C/T]CGGATTCTCCTATGA | 899 |
rs760281253 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2438946 | GAGGTTTTAGTTAGC[C/G]AAGATCGTGCCACTA | 899 |
rs760378621 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433302 | CCACTGACACGGGCC[C/T]GTGGTGCCTCCAGAG | 899 |
rs760391942 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452505 | GCGTTTATTCTCTTC[C/G]TCCTGAAGAAGTTAA | 899 |
rs760406917 | snp | C/T | 1.65828e-05 | 0.00287943 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445583 | TGCCGCGGTACAGGC[C/T]CCAGCTGCTGGGCAT | 899 |
rs760430087 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2432221 | CTTGAGGACAAATTC[C/T]ATGTAACATTTAACA | 899 |
rs760436368 | snp | A/G | 1.65121e-05 | 0.00287329 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2435834 | GGGAATTTCGAAGCT[A/G]CTGTGAAGCTGGGCA | 899 |
rs760457965 | in-del | -/CCACCCC | 3.31159e-05 | 0.00406901 | intron-variant | CCNF | GRCh38.p7 | 16:2449808 | ATCCCCTCCACCCCT[-/CCACCCC]GGCCTGCTTTCCTCC | 899 |
rs760464210 | snp | C/T | 1.80046e-05 | 0.00300033 | intron-variant | CCNF | GRCh38.p7 | 16:2449476 | GAGTAAGGAGTGGCC[C/T]TTCCCAGGGATGCCT | 899 |
rs760504975 | snp | A/G | 1.78787e-05 | 0.00298982 | intron-variant | CCNF | GRCh38.p7 | 16:2437079 | TGGAGAGCTTTCCAC[A/G]TTCCGTCCCTAAGAG | 899 |
rs760522485 | in-del | -/GAG | 1.77442e-05 | 0.00297855 | cds-indel, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456982 | CTATGCATACACAGT[-/GAG]GAGGAGGACATGAAC | 899 |
rs760533163 | snp | G/T | 1.77562e-05 | 0.00297956 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455479 | CCAGGAGGAGACGCT[G/T]CTGGGCAGCTTCCTC | 899 |
rs760551079 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438541 | AGCTACTCAGGAGGC[C/T]GAGGCAGGGAGAATT | 899 |
rs760553008 | snp | C/T | 1.64987e-05 | 0.00287212 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443636 | ACGCTCATGTTTGTC[C/T]TTTCTTCCTCAGCTG | 899 |
rs760556321 | snp | A/G | 3.29717e-05 | 0.00406015 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443772 | CAACAAGTCTTCTCC[A/G]TGCAGAAGGGACTCA | 899 |
rs760586153 | snp | A/G | 0.000102399 | 0.00715466 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455395 | CTCTCCACCTTGCAG[A/G]AAGCGGGAGAACAGC | 899 |
rs760625838 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2439890 | AGCCTTGGGGCAGGA[C/G]TATCTGGGCTCCCAC | 899 |
rs760743199 | snp | A/G | 3.47856e-05 | 0.00417032 | intron-variant | CCNF | GRCh38.p7 | 16:2439847 | GTGCGGGGCTGGGAT[A/G]ACGTGGGGAGCTGGC | 899 |
rs760771429 | snp | C/G | 2.08205e-05 | 0.00322643 | intron-variant | CCNF | GRCh38.p7 | 16:2449116 | GTGCCCAAAGCCATG[C/G]AGCAGGAGGCCACGG | 899 |
rs760830377 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2449055 | GGGCATTCAGCTTTC[C/T]TGCTGTGGGAGGGCC | 899 |
rs760896088 | snp | A/G | 1.6703e-05 | 0.00288985 | intron-variant | CCNF | GRCh38.p7 | 16:2449019 | TTAATCTTCGTTGTC[A/G]CTGTGCTGGAGGGTG | 899 |
rs760898059 | snp | C/T | 1.65548e-05 | 0.002877 | intron-variant | CCNF | GRCh38.p7 | 16:2453328 | CCTCCCTCCCGCCAC[C/T]TGGGCGTCTCATGGG | 899 |
rs760899204 | snp | A/G | 2.61633e-05 | 0.00361676 | intron-variant | CCNF | GRCh38.p7 | 16:2437333 | AGAGGGTGAGTCTGG[A/G]CGAGGGGCAGCACCT | 899 |
rs760953006 | snp | C/T | 3.30633e-05 | 0.00406578 | missense | CCNF | GRCh38.p7 | 16:2453247 | GACTACAGGCAAGTC[C/T]CTCTGACCGCCGTGA | 899 |
rs761023491 | snp | A/G | 4.99563e-05 | 0.00499756 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437239 | TTCATCTGGCTCTTC[A/G]TCCGCCCTCCGTGGT | 899 |
rs761074909 | snp | C/T | 1.65751e-05 | 0.00287876 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445459 | TTCTCTTTCCGCAGG[C/T]ACATTCTGATCGACT | 899 |
rs761107954 | snp | A/G | 1.86423e-05 | 0.003053 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456571 | AGCGGCATCCTCGAT[A/G]TCACCGTGGTCTACC | 899 |
rs761227016 | snp | A/G | 1.6534e-05 | 0.00287519 | intron-variant | CCNF | GRCh38.p7 | 16:2431308 | CTGCATGAAAACACT[A/G]TGAGCCCTAGCATTG | 899 |
rs761300716 | snp | A/G | 3.30699e-05 | 0.00406618 | missense | CCNF | GRCh38.p7 | 16:2453500 | ACAGGGGAGATCCAC[A/G]CCTTCCTCAGCTCTC | 899 |
rs761332818 | snp | C/T | 3.31752e-05 | 0.00407265 | intron-variant | CCNF | GRCh38.p7 | 16:2453551 | CGGTTAGTTACCCTG[C/T]GTTCTGGCTGCGCCA | 899 |
rs761337879 | snp | A/G | | | synonymous-codon | CCNF | GRCh38.p7 | 16:2455416 | GGAGAACAGCCTCCA[A/G]GAAGACAGAGGCAGC | 899 |
rs761385812 | in-del | -/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2454444 | GGGGCCTGGCCCTGG[-/C]CCCTGTGCTCAGCCT | 899 |
rs761471485 | snp | C/T | 2.40157e-05 | 0.00346515 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457032 | GTAAGTGTGTCAGCA[C/T]ATTTGCCGCAGTGGA | 899 |
rs761501929 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444625 | TTTTGAGACAGGGTC[-/T]TGGCTCTGTCACCCA | 899 |
rs761506948 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441104 | CTGGGCCTGGTGGCA[C/T]GTGCCTAGAGTCCCA | 899 |
rs761528479 | snp | A/C/G | 4.96498e-05 | 0.00498225 | intron-variant | CCNF | GRCh38.p7 | 16:2448838 | CTCCACCCTGAGACC[A/C/G]CTTCTCGGCGTTGCA | 899 |
rs761549429 | snp | A/T | 2.21816e-05 | 0.00333021 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439444 | TCCTCTGGGAAAGCG[A/T]CAGGAGGACAGATGT | 899 |
rs761552584 | in-del | -/T | 1.6495e-05 | 0.0028718 | intron-variant | CCNF | GRCh38.p7 | 16:2431098 | GAATAATTTTTCATC[-/T]TTATCAAGGCTTCTG | 899 |
rs761570242 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2431444 | GCACTTTGGGAGGCC[A/G]AAGGGGGGTGGATCA | 899 |
rs761621306 | snp | C/T | 0.000228968 | 0.0106973 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455563 | CGAGAAGGAGGGCGA[C/T]GGTGAGTGTGGGGCC | 899 |
rs761625786 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2437552 | TACACGTGCTGACAG[C/G]TGGAAACATGGGGCT | 899 |
rs761710479 | snp | C/T | 1.83105e-05 | 0.00302571 | intron-variant | CCNF | GRCh38.p7 | 16:2449487 | GGCCCTTCCCAGGGA[C/T]GCCTGTGTCGGGGAA | 899 |
rs761803003 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452419 | GTTCGCATGGGTCTC[A/G]TCCCACCCACCTTTG | 899 |
rs761837003 | snp | C/T | 1.75231e-05 | 0.00295994 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455494 | GCTGGGCAGCTTCCT[C/T]GACTGGAGCCTGGAC | 899 |
rs761900195 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2430525 | TTGGGACCTGAGCAA[C/T]AACCTTACTGCGTAG | 899 |
rs761909168 | snp | C/G | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457486 | ACAGCTGTGAGCACA[C/G]CACTGTCCCCTCATC | 899 |
rs761932467 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2448554 | TGAGACTATAGGCAC[A/G]TGCCACCATGCTCTG | 899 |
rs761971205 | snp | C/T | 0.00150887 | 0.0274255 | intron-variant | CCNF | GRCh38.p7 | 16:2449138 | AGGCCACGGTTGCAC[C/T]ACGTCGCCATCTGCG | 899 |
rs761997311 | snp | C/T | 7.37545e-05 | 0.00607222 | intron-variant | CCNF | GRCh38.p7 | 16:2449180 | CGCGTGCAGCATCGG[C/T]GTGAACATCATCCGG | 899 |
rs762016200 | snp | G/T | | | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456809 | GCTCCGTGGACGGTG[G/T]CTTGGGGGCCCTGCC | 899 |
rs762030951 | snp | A/G | 1.64741e-05 | 0.00286998 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443690 | TGCAAACCAGCTTGG[A/G]CTGGAGGTGAGAGCT | 899 |
rs762039769 | snp | A/G | 1.6757e-05 | 0.00289452 | intron-variant | CCNF | GRCh38.p7 | 16:2431043 | ATCATCTTCAGATGT[A/G]ACTTTTATCCTTTTT | 899 |
rs762067213 | snp | A/C | 6.59207e-05 | 0.00574073 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2438120 | AGTGCTGAGTCTGTT[A/C]GAGGTGAGTCAAGTT | 899 |
rs762107509 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435025 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCATGAGA | 899 |
rs762123353 | snp | G/T | 1.65509e-05 | 0.00287666 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453412 | AGCTTCCCCTCAGGT[G/T]CTGAGCTACAGCCAG | 899 |
rs762274702 | snp | A/C | 3.11522e-05 | 0.00394653 | intron-variant | CCNF | GRCh38.p7 | 16:2437346 | GGGCGAGGGGCAGCA[A/C]CTGCGAGGCCACCTG | 899 |
rs762281333 | snp | C/T | 1.67248e-05 | 0.00289173 | stop-gained, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456685 | CTGGCGCTGGACACC[C/T]AGATCCCTGCAACCC | 899 |
rs762316937 | in-del | -/T | 1.66092e-05 | 0.00288172 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443825 | TCAGGCCGGGGCTTC[-/T]AATCAGAGCGGCGCG | 899 |
rs762393594 | in-del | -/AG | 1.98948e-05 | 0.00315388 | intron-variant | CCNF | GRCh38.p7 | 16:2449081 | GGGCCTCATGGACTC[-/AG]AGAGCAGCTGTCTCT | 899 |
rs762401295 | snp | C/T | 1.65045e-05 | 0.00287263 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445519 | TTCACAAGCCTGTGC[C/T]TGCACCTGACCGTGG | 899 |
rs762408878 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454499 | AGGCCCCCCACAGCC[C/T]CATCAGTCTTCTGAG | 899 |
rs762467934 | snp | C/T | 1.79528e-05 | 0.00299601 | intron-variant, missense | CCNF | GRCh38.p7 | 16:2433012 | GCCAGTGTGTGGGCA[C/T]GTGCCAGCTTCCAGG | 899 |
rs762468749 | in-del | -/GCTGGCAGGGACGT | 1.76883e-05 | 0.00297386 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445643 | AGCCCCCTTGGCCCA[-/GCTGGCAGGGACGT]GCTGGCAGGGACGTG | 899 |
rs762484860 | snp | A/G | 1.70101e-05 | 0.00291629 | missense | CCNF | GRCh38.p7 | 16:2449405 | AGCCTGTCCGCCTAC[A/G]CCCCAGCCCGCCTGG | 899 |
rs762508687 | in-del | -/CTCCATCCT | 0.000511978 | 0.0159915 | intron-variant | CCNF | GRCh38.p7 | 16:2449798 | CGTCCCCTCCATCCC[-/CTCCATCCT]CTCCACCCCTGGCCT | 899 |
rs762603366 | snp | A/G | 1.6766e-05 | 0.00289529 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439813 | ACGCTGCCAAAGGCT[A/G]CTGGGAAGCGCAGGT | 899 |
rs762663630 | snp | C/T | 0.000122163 | 0.00781451 | missense, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456974 | GGATAAACCTATGCA[C/T]ACACAGTGAGGAGGA | 899 |
rs762693375 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454361 | TGTCACTCCACACAC[A/G]CACCGACTCCCTGGG | 899 |
rs762716472 | snp | C/G | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443513 | AGCCATCCTTGTTCC[C/G]GAAGCTTGTGAAGGT | 899 |
rs762782804 | snp | C/T | 3.29707e-05 | 0.00406008 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448921 | CAACACTTACAAGTA[C/T]GAGGACCTGGTGAGA | 899 |
rs762797149 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428652 | TCTGGCCAAAGTGAT[A/G]GGGAGGGCTTGCCCC | 899 |
rs762829557 | snp | A/G | 1.64803e-05 | 0.00287052 | intron-variant | CCNF | GRCh38.p7 | 16:2449938 | TTGGCCGGGCGCAGA[A/G]GCTCATGCCTGTAAC | 899 |
rs762977300 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2430883 | AAGTTACATGACATG[A/C]GCTATTTGCCATAAA | 899 |
rs763031135 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438430 | TGGGCCTCTCCTGCT[C/T]GTGTGGACCTCTCTG | 899 |
rs763031251 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | CCNF | GRCh38.p7 | 16:2449879 | GATTCTCCTATGAAG[A/G]CCTCATTCCCTGCGT | 899 |
rs763103851 | snp | C/T | 4.95356e-05 | 0.00497648 | missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443797 | GACTCAATGACACAA[C/T]GAGGTGAGGCATTCA | 899 |
rs763145280 | snp | C/T | 1.68417e-05 | 0.00290182 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443852 | CGCGGAAGCCAGCCT[C/T]CAGGGGAAGGGAGCC | 899 |
rs763157555 | snp | G/T | 7.16102e-05 | 0.00598331 | intron-variant | CCNF | GRCh38.p7 | 16:2455576 | GACGGTGAGTGTGGG[G/T]CCAGGGTGCACCAGA | 899 |
rs763246948 | snp | C/T | | | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447067 | GACGACTGAGGAGGT[C/T]GGGCGGCCGCCTCCC | 899 |
rs763286892 | snp | C/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428858 | AGCAGGCGGCGGAAG[C/G]GAAGGCCGTGCAAGC | 899 |
rs763419880 | snp | A/G | 9.92539e-05 | 0.00704394 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456837 | GCCCCAACCTACCTC[A/G]GTGCTGTCCCTGGAC | 899 |
rs763420643 | snp | G/T | 1.67379e-05 | 0.00289287 | intron-variant | CCNF | GRCh38.p7 | 16:2431048 | CTTCAGATGTAACTT[G/T]TATCCTTTTTTTTTC | 899 |
rs763454851 | snp | C/G | 2.22864e-05 | 0.00333807 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439404 | GAGGAGGCTGCTCAT[C/G]AGGGATGTCTGACCA | 899 |
rs763485117 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2448353 | GCTGCTTTCTGTCTG[C/T]CTTGTGGCTCTCATC | 899 |
rs763547394 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2433636 | TCTGTCACCAGGCTG[A/G]AGTGCAGTGGTGCAA | 899 |
rs763581056 | snp | C/G | 1.64808e-05 | 0.00287057 | intron-variant | CCNF | GRCh38.p7 | 16:2438136 | GAGGTGAGTCAAGTT[C/G]TTCTCTGCACTGGGA | 899 |
rs763592119 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440842 | GCCTGCAATCCCAGC[A/G]CTGTAGGAGGTTGAG | 899 |
rs763656931 | snp | C/G | 1.64732e-05 | 0.0028699 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431185 | AAAGCGAAGAATAAG[C/G]AGGAGGCCCCGAAAC | 899 |
rs763665994 | snp | G/T | 4.30478e-05 | 0.00463919 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439436 | CTCCTACCTCCTCTG[G/T]GAAAGCGACAGGAGG | 899 |
rs763679290 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454415 | CCATGCAGATACGCA[C/T]GGCTACTCCAGGAGG | 899 |
rs763692643 | snp | A/G | 1.65427e-05 | 0.00287595 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453427 | GCTGAGCTACAGCCA[A/G]TTGTGTGCTGCATTA | 899 |
rs763694348 | snp | C/T | 1.66244e-05 | 0.00288304 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445591 | TACAGGCTCCAGCTG[C/T]TGGGCATCGCCTGCA | 899 |
rs763732427 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2453835 | GGCTCTAGCCCTGCC[C/T]GTGCCTGTCATGCGC | 899 |
rs763743574 | snp | A/G | 3.30606e-05 | 0.00406561 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456853 | GTGCTGTCCCTGGAC[A/G]GTGACTCGCACACAC | 899 |
rs763798501 | in-del | -/GTG | 1.64768e-05 | 0.00287021 | cds-indel | CCNF | GRCh38.p7 | 16:2449913 | GAGCCTCCATAAGAA[-/GTG]GTGAGTTTTGGCCGG | 899 |
rs763809619 | snp | A/C | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428842 | AAGGGTCTCCACCTG[A/C]AGCAGGCGGCGGAAG | 899 |
rs763834608 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2439004 | CTCTGCCTCAACAAC[A/G]ACAAAAAAACCAGCC | 899 |
rs764007699 | in-del | -/TGGGCTGGG | | | intron-variant | CCNF | GRCh38.p7 | 16:2440949 | TTAAAATTAGCTGGA[-/TGGGCTGGG]TGCAAGTGGCTCATG | 899 |
rs764030107 | snp | A/T | 2.19841e-05 | 0.00331535 | intron-variant | CCNF | GRCh38.p7 | 16:2433071 | GCTCTTTGAAAGGTA[A/T]CTCTGCACCCTGAGA | 899 |
rs764061587 | snp | C/T | 1.65116e-05 | 0.00287324 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2435835 | GGAATTTCGAAGCTG[C/T]TGTGAAGCTGGGCAT | 899 |
rs764083211 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438443 | CTCGTGTGGACCTCT[C/T]TGCCTGGCCAAAATG | 899 |
rs764089161 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444301 | GCTTTCTTCAGTTAC[-/T]TTTTTTTTTTTTTTT | 899 |
rs764146512 | in-del | -/GGTGGCTTGGGGGCCCTGCCCC | 1.80873e-05 | 0.00300721 | frameshift-variant, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456988 | TACACAGTGAGGAGG[-/GGTGGCTTGGGGGCCCTGCCCC]AGGACATGAACCTGG | 899 |
rs764189073 | in-del | -/C | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429326 | CGGGGCCGGCGGCGG[-/C]CCCCCCCGGGCAGGC | 899 |
rs764227871 | snp | A/C | 1.64749e-05 | 0.00287005 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443681 | CTGTGCAAATGCAAA[A/C]CAGCTTGGACTGGAG | 899 |
rs764280724 | snp | C/T | 2.0864e-05 | 0.00322979 | intron-variant | CCNF | GRCh38.p7 | 16:2449129 | TGGAGCAGGAGGCCA[C/T]GGTTGCACCACGTCG | 899 |
rs764282881 | snp | C/T | 1.74427e-05 | 0.00295314 | intron-variant | CCNF | GRCh38.p7 | 16:2439849 | GCGGGGCTGGGATGA[C/T]GTGGGGAGCTGGCCT | 899 |
rs764342076 | snp | C/G | | | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447794 | AGCTGCCCCCCACCT[C/G]TGCTCTCAGAGGTGC | 899 |
rs764358145 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2446296 | GGAGGGTGGCAGTTG[A/G]CTGCCCTTCTCTGAA | 899 |
rs764394555 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2433642 | ACCAGGCTGGAGTGC[A/G]GTGGTGCAATCTCAG | 899 |
rs764400572 | snp | A/T | 3.29712e-05 | 0.00406011 | intron-variant | CCNF | GRCh38.p7 | 16:2449964 | GTAACCCCAGCACTT[A/T]GGGAGGCCGAGGCGG | 899 |
rs764409306 | snp | G/T | 3.34096e-05 | 0.00408702 | intron-variant | CCNF | GRCh38.p7 | 16:2449021 | AATCTTCGTTGTCGC[G/T]GTGCTGGAGGGTGGG | 899 |
rs764445847 | snp | C/T | 1.66824e-05 | 0.00288806 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437242 | ATCTGGCTCTTCATC[C/T]GCCCTCCGTGGTCGG | 899 |
rs764448065 | snp | C/G | | | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447198 | TGAGTCCAATTTCTT[C/G]CCCAACCACAAGACC | 899 |
rs764545606 | snp | A/G | 1.66763e-05 | 0.00288753 | missense | CCNF | GRCh38.p7 | 16:2449324 | GTCCTGCTGACGCTA[A/G]TCCCTGTGGAGCTGA | 899 |
rs764553387 | snp | C/G | 1.67298e-05 | 0.00289217 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456681 | GGCACTGGCGCTGGA[C/G]ACCCAGATCCCTGCA | 899 |
rs764562957 | in-del | -/C | 1.66513e-05 | 0.00288537 | intron-variant | CCNF | GRCh38.p7 | 16:2431062 | TTATCCTTTTTTTTT[-/C]CCCTTCAAGGGTGTG | 899 |
rs764819593 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2433475 | CCCCGCACCCTGGCC[A/C]CTGTTCACATGTGCT | 899 |
rs764827616 | snp | C/G/T | 8.35086e-05 | 0.00646128 | intron-variant | CCNF | GRCh38.p7 | 16:2449266 | TGAGAGCCCACACCC[C/G/T]GTCCCGGCTGTCTAG | 899 |
rs764833744 | in-del | -/TCCCTAAGAGACA | | | intron-variant | CCNF | GRCh38.p7 | 16:2437085 | GCTTTCCACATTCCG[-/TCCCTAAGAGACA]TCCCTGGGCTCTGTC | 899 |
rs764855503 | in-del | -/T | 1.64822e-05 | 0.00287068 | intron-variant | CCNF | GRCh38.p7 | 16:2431116 | ATCAAGGCTTCTGTC[-/T]TTTTTTCCTTCAGTG | 899 |
rs764857901 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2453599 | CGTGCCGGCCCAGTT[A/C]CCTCAGCGCTTCCTC | 899 |
rs764862418 | snp | C/T | 6.63306e-05 | 0.00575855 | intron-variant | CCNF | GRCh38.p7 | 16:2431329 | CCTAGCATTGTTGAT[C/T]ATACCATCAGGCCTT | 899 |
rs764898739 | snp | A/G | 2.25497e-05 | 0.00335773 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439450 | GGGAAAGCGACAGGA[A/G]GACAGATGTGAGTGG | 899 |
rs764919488 | snp | A/C | 1.81817e-05 | 0.00301504 | intron-variant | CCNF | GRCh38.p7 | 16:2439708 | TCTGAGTTCCTCCCA[A/C]GACACAGTTGTACAA | 899 |
rs764920424 | snp | A/C | 1.65359e-05 | 0.00287536 | missense | CCNF | GRCh38.p7 | 16:2453501 | CAGGGGAGATCCACG[A/C]CTTCCTCAGCTCTCC | 899 |
rs764967061 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427579 | CTCACTACCCATAAC[A/G]TTTTCAACCGACACC | 899 |
rs765023445 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2440124 | CTGTCAAAATTTGTG[C/T]CATTCTTGAAAGTTG | 899 |
rs765036806 | snp | C/T | 3.44804e-05 | 0.00415199 | synonymous-codon, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456966 | GGTGAAGCGGATAAA[C/T]CTATGCATACACAGT | 899 |
rs765072519 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441214 | ACTCCAGCCTGGCAA[C/T]AGAGCGATACTCCAT | 899 |
rs765151794 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | CCNF | GRCh38.p7 | 16:2449875 | ACCGGATTCTCCTAT[A/G]AAGACCTCATTCCCT | 899 |
rs765152283 | snp | A/G | 1.67318e-05 | 0.00289234 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445606 | CTGGGCATCGCCTGC[A/G]TGGTCATCTGCACCC | 899 |
rs765205100 | snp | A/G/T | 3.67865e-05 | 0.00428861 | intron-variant | CCNF | GRCh38.p7 | 16:2449488 | GCCCTTCCCAGGGAT[A/G/T]CCTGTGTCGGGGAAG | 899 |
rs765208647 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458568 | AAATGCTCTTGAACC[A/G]GAAACCCAGGGATGG | 899 |
rs765240595 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2451035 | GGCCCCTCCGCCCTT[A/C]TCTCTGGTGAGCCTG | 899 |
rs765259053 | snp | A/G | 1.74805e-05 | 0.00295634 | missense | CCNF | GRCh38.p7 | 16:2455495 | CTGGGCAGCTTCCTC[A/G]ACTGGAGCCTGGACT | 899 |
rs765356040 | snp | A/C | 1.77944e-05 | 0.00298276 | intron-variant | CCNF | GRCh38.p7 | 16:2437100 | TCCCTAAGAGACATC[A/C]CTGGGCTCTGTCCTG | 899 |
rs765422854 | snp | C/T | 1.65154e-05 | 0.00287358 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2435863 | CATAGCCTACCTCTA[C/T]AATGAAGGCCGTAAG | 899 |
rs765541767 | snp | A/G | 0.000906792 | 0.0212738 | intron-variant | CCNF | GRCh38.p7 | 16:2449029 | TTGTCGCTGTGCTGG[A/G]GGGTGGGGGTGGGCA | 899 |
rs765542237 | snp | C/G | 1.64738e-05 | 0.00286995 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443701 | TTGGACTGGAGGTGA[C/G]AGCTTCCAGTGAGAT | 899 |
rs765574299 | snp | C/G/T | 0.000133976 | 0.00818372 | intron-variant | CCNF | GRCh38.p7 | 16:2431045 | CATCTTCAGATGTAA[C/G/T]TTTTATCCTTTTTTT | 899 |
rs765620854 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2456236 | TGCAAACCCCAGGCA[C/G]ACTGCGGGGTCCTTG | 899 |
rs765654180 | snp | C/G | 1.65674e-05 | 0.00287809 | intron-variant | CCNF | GRCh38.p7 | 16:2453342 | CCTGGGCGTCTCATG[C/G]GGTGCTGGGGTGTGG | 899 |
rs765788059 | snp | A/G | 1.67184e-05 | 0.00289118 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456688 | GCGCTGGACACCCAG[A/G]TCCCTGCAACCCCTG | 899 |
rs765812496 | in-del | -/G | 1.64838e-05 | 0.00287083 | frameshift-variant | CCNF | GRCh38.p7 | 16:2448887 | CCTGACCATCCGGGA[-/G]GGCCGTATGGCTCAC | 899 |
rs765916287 | snp | G/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445364 | CCAGAGCTAGCCAGC[G/T]TATTTGGTCGGGCCC | 899 |
rs765980912 | snp | A/G | 1.8282e-05 | 0.00302336 | intron-variant, missense | CCNF | GRCh38.p7 | 16:2433027 | TGTGCCAGCTTCCAG[A/G]AGCTGTGGCCGTCTC | 899 |
rs765990336 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2430650 | CTCTCCAGGGCCGAC[C/G]CTTCTAATTTGGACT | 899 |
rs766000646 | snp | A/G | 1.70171e-05 | 0.00291689 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449410 | GTCCGCCTACGCCCC[A/G]GCCCGCCTGGCTGCC | 899 |
rs766071562 | snp | A/G | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457974 | AAGAGCAGAGCAGTC[A/G]GGGGCCGTGTCCTGG | 899 |
rs766112444 | in-del | -/TGCCGGGG | | | intron-variant | CCNF | GRCh38.p7 | 16:2435482 | CCTAGCTACTTGGGA[-/TGCCGGGG]TGGGAGAATGGCTTA | 899 |
rs766120944 | snp | A/G | 5.13848e-05 | 0.00506851 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457042 | CAGCACATTTGCCGC[A/G]GTGGATGTGTACTGA | 899 |
rs766126024 | snp | C/T | 3.36638e-05 | 0.00410253 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439822 | AAGGCTGCTGGGAAG[C/T]GCAGGTGAGGTGCGG | 899 |
rs766126161 | snp | A/G | 5.85206e-05 | 0.00540896 | intron-variant | CCNF | GRCh38.p7 | 16:2432921 | TGGGGCTTTTGGGTG[A/G]TGCCTCCATCACCCA | 899 |
rs766136327 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2438552 | AGGCTGAGGCAGGGA[A/G]AATTGCTTGAACCTG | 899 |
rs766162997 | snp | A/T | 1.80166e-05 | 0.00300133 | intron-variant | CCNF | GRCh38.p7 | 16:2439717 | CTCCCAAGACACAGT[A/T]GTACAAAGGCTCGGT | 899 |
rs766171799 | snp | C/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445284 | TGGGGCTGGGACCCA[C/T]GGAGCCTCCCGGGCT | 899 |
rs766192108 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452541 | TTTCCAAACAAGATA[A/G]ATTAGAAACGTTATT | 899 |
rs766285320 | snp | A/G | 1.75758e-05 | 0.00296438 | missense, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456977 | TAAACCTATGCATAC[A/G]CAGTGAGGAGGAGGA | 899 |
rs766287976 | snp | A/G | 0.000117067 | 0.00764983 | intron-variant | CCNF | GRCh38.p7 | 16:2439460 | CAGGAGGACAGATGT[A/G]AGTGGTGCCTGCTCT | 899 |
rs766293412 | in-del | -/T | 2.0479e-05 | 0.00319986 | intron-variant, frameshift-variant | CCNF | GRCh38.p7 | 16:2433060 | GGGAACCTGAAGCTC[-/T]TTGAAAGGTATCTCT | 899 |
rs766324204 | snp | A/G/T | 3.29762e-05 | 0.00406045 | missense | CCNF | GRCh38.p7 | 16:2448940 | GACCTGGTGAGAATG[A/G/T]TGGGCGAGATCGTCT | 899 |
rs766340988 | snp | A/G | 1.65362e-05 | 0.00287538 | intron-variant | CCNF | GRCh38.p7 | 16:2448845 | CTGAGACCCCTTCTC[A/G]GCGTTGCAGGTTTAT | 899 |
rs766378210 | snp | A/C | 0.000133527 | 0.0081698 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437166 | CGCAGAAGTGAATGG[A/C]CTGAAGGCCTCTCGC | 899 |
rs766390922 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449880 | ATTCTCCTATGAAGA[C/T]CTCATTCCCTGCGTC | 899 |
rs766499506 | snp | A/G | 1.88813e-05 | 0.0030725 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445343 | TTCCAGGGTAAACCC[A/G]TGATTCCAGAGCTAG | 899 |
rs766547417 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449862 | GCTGTGGGACCTCAC[C/T]GGATTCTCCTATGAA | 899 |
rs766694135 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2436937 | CACAATGACCCACCT[A/G]TTCTAGACATTAATG | 899 |
rs766705424 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454096 | TGCTGGCCCTGCGCC[A/G]TGACCCCTCAGCACC | 899 |
rs766763090 | snp | C/T | 1.66613e-05 | 0.00288623 | intron-variant | CCNF | GRCh38.p7 | 16:2431059 | ACTTTTATCCTTTTT[C/T]TTTCCCTTCAAGGGT | 899 |
rs766844201 | snp | C/T | 1.65416e-05 | 0.00287586 | synonymous-codon, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456841 | CAACCTACCTCAGTG[C/T]TGTCCCTGGACAGTG | 899 |
rs766865135 | snp | A/G | 2.01623e-05 | 0.00317502 | intron-variant | CCNF | GRCh38.p7 | 16:2449153 | CACGTCGCCATCTGC[A/G]CTGGTGCGCTACGCG | 899 |
rs766866763 | snp | A/G | 1.65471e-05 | 0.00287633 | missense | CCNF | GRCh38.p7 | 16:2453420 | CTCAGGTGCTGAGCT[A/G]CAGCCAGTTGTGTGC | 899 |
rs766966078 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2456177 | AGGTGTGCCCACGTG[A/G]TATACGTGACACTCC | 899 |
rs766999013 | snp | A/G | 6.11303e-05 | 0.00552824 | utr-variant-5-prime, intron-variant | CCNF | GRCh38.p7 | 16:2429470 | TCCGGCGGCAGCGAC[A/G]CGAGCGCGGCGATGG | 899 |
rs767098403 | snp | C/T | 1.64811e-05 | 0.00287059 | intron-variant | CCNF | GRCh38.p7 | 16:2438141 | GAGTCAAGTTGTTCT[C/T]TGCACTGGGACTTTG | 899 |
rs767126159 | snp | A/G | 5.11889e-05 | 0.00505883 | missense | CCNF | GRCh38.p7 | 16:2449415 | CCTACGCCCCAGCCC[A/G]CCTGGCTGCCGCAGC | 899 |
rs767153384 | snp | C/G | 3.71243e-05 | 0.00430822 | intron-variant | CCNF | GRCh38.p7 | 16:2437361 | CCTGCGAGGCCACCT[C/G]CAGGGTCCCAGGACA | 899 |
rs767165875 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441581 | CTCTGTTGCCCAGGC[G/T]AGAGCACAGTGGTGC | 899 |
rs767206901 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2438855 | ACACAAAAATTAGCC[A/G]GGCATGGTGGTGGGC | 899 |
rs767248552 | snp | C/T | 4.84943e-05 | 0.0049239 | intron-variant | CCNF | GRCh38.p7 | 16:2455378 | ACTGGGTCTCCTGGG[C/T]TCTCTCCACCTTGCA | 899 |
rs767259178 | snp | A/C | 3.30256e-05 | 0.00406346 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2435829 | AAAAGGGGAATTTCG[A/C]AGCTGCTGTGAAGCT | 899 |
rs767276351 | snp | A/G | 1.65048e-05 | 0.00287265 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445533 | CCTGCACCTGACCGT[A/G]GAGTGTGTGGACCGG | 899 |
rs767404667 | in-del | -/CCTCCACT | 1.64977e-05 | 0.00287203 | intron-variant | CCNF | GRCh38.p7 | 16:2449805 | TCCATCCCCTCCACC[-/CCTCCACT]CCTGGCCTGCTTTCC | 899 |
rs767409966 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2452467 | TCGTCCCAACCCTGG[C/T]CACCAAAAGCTGTTT | 899 |
rs767479332 | snp | A/G | 3.42091e-05 | 0.00413562 | intron-variant | CCNF | GRCh38.p7 | 16:2439836 | GCGCAGGTGAGGTGC[A/G]GGGCTGGGATGACGT | 899 |
rs767494706 | in-del | -/AC | 1.69335e-05 | 0.00290972 | frameshift-variant | CCNF | GRCh38.p7 | 16:2449385 | GCTCTCCCTGCTGCA[-/AC]CACCAGCCTGTCCGC | 899 |
rs767502488 | snp | A/G | 2.70838e-05 | 0.00367983 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457049 | TTTGCCGCAGTGGAT[A/G]TGTACTGAGGGGGCT | 899 |
rs767534481 | snp | C/T | 1.66435e-05 | 0.0028847 | intron-variant | CCNF | GRCh38.p7 | 16:2449015 | CTTATTAATCTTCGT[C/T]GTCGCTGTGCTGGAG | 899 |
rs767612557 | snp | C/T | 1.65803e-05 | 0.00287922 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437226 | GGGTGCCGCACCTTT[C/T]ATCTGGCTCTTCATC | 899 |
rs767670799 | snp | A/C | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458484 | CGAACTCATGACCTC[A/C]AGTGATCCGCCCACT | 899 |
rs767687539 | in-del | -/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2430842 | CTGTCATGTGGGCTC[-/T]TGGATCAGAAAGTTT | 899 |
rs767697648 | snp | A/G | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445694 | GGTCACCTGCCCTTC[A/G]TGTGCTCCTCACTGG | 899 |
rs767728162 | snp | A/C | 0.000531429 | 0.0162921 | missense | CCNF | GRCh38.p7 | 16:2453241 | CCCAAGGACTACAGG[A/C]AAGTCTCTCTGACCG | 899 |
rs767832305 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2433657 | AGTGGTGCAATCTCA[A/G]CTCACTGCAACCACC | 899 |
rs767883143 | snp | C/G | 1.88838e-05 | 0.00307271 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445349 | GGTAAACCCATGATT[C/G]CAGAGCTAGCCAGCT | 899 |
rs767884579 | snp | A/T | 1.66189e-05 | 0.00288256 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437171 | AAGTGAATGGCCTGA[A/T]GGCCTCTCGCTTCTT | 899 |
rs767910393 | snp | C/T | 9.43405e-05 | 0.00686741 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456567 | TCCCAGCGGCATCCT[C/T]GATGTCACCGTGGTC | 899 |
rs767962309 | snp | C/T | 3.30682e-05 | 0.00406608 | missense | CCNF | GRCh38.p7 | 16:2453497 | AGCACAGGGGAGATC[C/T]ACGCCTTCCTCAGCT | 899 |
rs768027950 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2446521 | TTCCGCCTTTGGAAA[C/T]AACGTGGAAATGATT | 899 |
rs768061407 | snp | C/T | 5.15779e-05 | 0.00507802 | intron-variant | CCNF | GRCh38.p7 | 16:2449207 | CCGGGCCAGACCCTG[C/T]GCTGGGCCTGCATGC | 899 |
rs768076060 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454515 | CATCAGTCTTCTGAG[A/G]CAGACCCCCACGGGT | 899 |
rs768080881 | snp | A/G | 1.69942e-05 | 0.00291493 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456956 | CCCAGCAACAGGTGA[A/G]GCGGATAAACCTATG | 899 |
rs768114267 | snp | C/T | 0.00013653 | 0.00826115 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437262 | TCCGTGGTCGGTGAG[C/T]GGAAGCTGCTGCAAG | 899 |
rs768162382 | snp | A/C | 3.3018e-05 | 0.00406299 | intron-variant | CCNF | GRCh38.p7 | 16:2448987 | GATTCGAGTAAGCAG[A/C]GGTTCCATTTTCCTT | 899 |
rs768281680 | snp | C/G/T | 3.29572e-05 | 0.00405928 | intron-variant | CCNF | GRCh38.p7 | 16:2449928 | GTGGTGAGTTTTGGC[C/G/T]GGGCGCAGAGGCTCA | 899 |
rs768333118 | snp | C/T | 1.67612e-05 | 0.00289488 | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456495 | TGGCAGGGGGTCTCC[C/T]CTGATGCTTGGGTGT | 899 |
rs768438236 | snp | C/T | 1.70464e-05 | 0.0029194 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437147 | CTGTGTCTGATGAGG[C/T]CCGCGCAGAAGTGAA | 899 |
rs768465824 | snp | C/T | 5.26219e-05 | 0.00512915 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455560 | GGGCGAGAAGGAGGG[C/T]GACGGTGAGTGTGGG | 899 |
rs768492901 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2455282 | GTAGCAGAACCTTTG[A/G]GAGCACGTGGTGACA | 899 |
rs768511877 | snp | A/G | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443514 | GCCATCCTTGTTCCC[A/G]AAGCTTGTGAAGGTT | 899 |
rs768513550 | in-del | -/TT | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445728 | GTTTTGTTTTGTGTT[-/TT]GTTTTTTTTTTTTTC | 899 |
rs768516256 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2431296 | AGCTGTAAGTCCCTG[C/T]ATGAAAACACTATGA | 899 |
rs768572360 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2455995 | TGGGTGACACAGCAA[G/T]ACAAAAAATTTAAAA | 899 |
rs768639357 | snp | C/T | 5.03749e-05 | 0.00501846 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443839 | CTAATCAGAGCGGCG[C/T]GGAAGCCAGCCTCCA | 899 |
rs768688650 | snp | C/G | 1.69072e-05 | 0.00290746 | intron-variant | CCNF | GRCh38.p7 | 16:2449227 | GGCCTGCATGCGGCA[C/G]TGCACCAAGGAGCCC | 899 |
rs768732648 | snp | A/G | 7.30367e-05 | 0.0060426 | intron-variant | CCNF | GRCh38.p7 | 16:2439698 | GGGTCTTGGTTCTGA[A/G]TTCCTCCCAAGACAC | 899 |
rs768793571 | snp | A/G | 1.68903e-05 | 0.00290601 | intron-variant | CCNF | GRCh38.p7 | 16:2431019 | GGCACAGGGAATAGT[A/G]ACCATTAGATCATCT | 899 |
rs768796512 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2441082 | ACTAAAAATACAAAA[A/G]AATTAGCTGGGCCTG | 899 |
rs768832394 | snp | C/T | 1.64838e-05 | 0.00287083 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2438086 | CTCACAAAGCATCCA[C/T]ATTGCACTGCTTGGG | 899 |
rs768849807 | snp | C/G | 1.65323e-05 | 0.00287505 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445562 | GGTACCTGCGGAGGA[C/G]GCTGGTGCCGCGGTA | 899 |
rs768922579 | snp | G/T | 1.65614e-05 | 0.00287757 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456815 | TGGACGGTGGCTTGG[G/T]GGCCCTGCCCCAACC | 899 |
rs768968149 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2436737 | TGTGCAGCCATTGCC[A/G]CTGTCTAATTTTAGA | 899 |
rs769039044 | snp | A/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459157 | GCTGCCTGGGTCCCA[A/G]CCTCCCTGACAACTC | 899 |
rs769069786 | snp | C/T | 1.65061e-05 | 0.00287277 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445512 | GAAGGACTTCACAAG[C/T]CTGTGCCTGCACCTG | 899 |
rs769097211 | in-del | -/GACAGG | | | intron-variant | CCNF | GRCh38.p7 | 16:2435105 | AAATAGAAAAAATTA[-/GACAGG]CGTGGTGGCGGGCAC | 899 |
rs769146199 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2434755 | CCCCATCAGCAGTCA[C/T]TTCCCATTTTCCCCA | 899 |
rs769214656 | snp | A/C/G/T | 0.000194058 | 0.00984854 | intron-variant | CCNF | GRCh38.p7 | 16:2449194 | GCGTGAACATCATCC[A/C/G/T]GGCCAGACCCTGCGC | 899 |
rs769252336 | snp | A/G | 1.66571e-05 | 0.00288587 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439783 | GCCTCCACAGCTTCC[A/G]AAAACTCAGGGACTA | 899 |
rs769263218 | in-del | -/TCCA | 1.65438e-05 | 0.00287605 | intron-variant | CCNF | GRCh38.p7 | 16:2449790 | ATCCCCTCCGTCCCC[-/TCCA]TCCATCCCCTCCACC | 899 |
rs769269374 | snp | C/T | 3.64272e-05 | 0.00426758 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455443 | CAGCTTCGTTACCAC[C/T]CCCACTGCGGAGCTG | 899 |
rs769286504 | snp | C/T | 8.3013e-05 | 0.00644202 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443608 | TGGAAAACTGCAACA[C/T]GGCTGCTGTCTCACG | 899 |
rs769324348 | snp | A/G | 4.97014e-05 | 0.0049848 | intron-variant | CCNF | GRCh38.p7 | 16:2455350 | GCCTGGCCTCCCAGC[A/G]CCGCCGTCCATGACT | 899 |
rs769349067 | in-del | -/TTC | 1.64974e-05 | 0.00287201 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443638 | GCTCATGTTTGTCTT[-/TTC]TTCCTCAGCTGTCTT | 899 |
rs769388208 | in-del | -/TC | | | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446793 | CATCTCCCATCTTAA[-/TC]TCTGCCACCAACTAG | 899 |
rs769410689 | snp | A/G | 1.65138e-05 | 0.00287343 | intron-variant | CCNF | GRCh38.p7 | 16:2448994 | GTAAGCAGCGGTTCC[A/G]TTTTCCTTATTAATC | 899 |
rs769456035 | in-del | -/GCG | 1.6675e-05 | 0.00288743 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443833 | GGGCTTCTAATCAGA[-/GCG]GCGCGGAAGCCAGCC | 899 |
rs769508433 | snp | A/C | 2.39943e-05 | 0.00346361 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457033 | TAAGTGTGTCAGCAC[A/C]TTTGCCGCAGTGGAT | 899 |
rs769537532 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | CCNF | GRCh38.p7 | 16:2448902 | AGGCCGTATGGCTCA[C/T]GGACAACACTTACAA | 899 |
rs769537549 | snp | C/T | 1.65751e-05 | 0.00287876 | intron-variant | CCNF | GRCh38.p7 | 16:2453195 | CATGTCCACTCCACG[C/T]GACTCTGTTTCCAGC | 899 |
rs769587346 | snp | C/T | 9.88696e-05 | 0.00703029 | intron-variant | CCNF | GRCh38.p7 | 16:2449932 | TGAGTTTTGGCCGGG[C/T]GCAGAGGCTCATGCC | 899 |
rs769600079 | snp | C/T | 0.000174847 | 0.00934841 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445414 | GCAGACAGGGACACA[C/T]GGAGAACGCCCCCAC | 899 |
rs769612325 | snp | C/T | 4.28156e-05 | 0.00462666 | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456537 | CCTCCCCACCAACCT[C/T]CCTGCAGTGACAGCT | 899 |
rs769636029 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454305 | CAAGAAGCGTGACAG[C/T]ACTTTCCATTGTGTG | 899 |
rs769642353 | snp | A/G | 1.71349e-05 | 0.00292697 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456625 | CAGGAATCCAGTGAT[A/G]AGGAGGCTTGTCCAG | 899 |
rs769707922 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2430054 | GAATATTTTATGGAG[A/C]GGTCTATAGAATCTT | 899 |
rs769712586 | snp | A/G | 1.66654e-05 | 0.00288659 | missense | CCNF | GRCh38.p7 | 16:2449288 | GCTGTCTAGGTCCCC[A/G]CTGTGGTGGATTACA | 899 |
rs769783592 | snp | C/G | 1.65397e-05 | 0.00287569 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437211 | TGAGCGGCTGAATGT[C/G]GGTGCCGCACCTTTC | 899 |
rs769821601 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2453949 | CGCCACCCGTGTGGA[C/T]CTGTTTACCCGCCTC | 899 |
rs769872165 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452377 | CCCTGTGCCTTCTGG[A/G]CAAGGAACGAGGCTG | 899 |
rs769881023 | snp | C/G | 1.64743e-05 | 0.00287 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431137 | TCCTTCAGTGGTCCA[C/G]TGTAGGTGTGCCAAG | 899 |
rs769943231 | snp | C/G/T | 6.72851e-05 | 0.0057999 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443850 | GGCGCGGAAGCCAGC[C/G/T]TCCAGGGGAAGGGAG | 899 |
rs769952836 | snp | C/T | | | missense | CCNF | GRCh38.p7 | 16:2453227 | TCCATGATGACGCCC[C/T]CAAGGACTACAGGCA | 899 |
rs769973967 | in-del | -/GAGGGCACACT | | | intron-variant | CCNF | GRCh38.p7 | 16:2430565 | CCGCATTCTACAATA[-/GAGGGCACACT]GAGACTCTGCAGAGC | 899 |
rs769980414 | snp | A/T | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431227 | GAGTCTCCCCGAAGA[A/T]GTGCTCTTTCACATC | 899 |
rs770009969 | snp | A/T | 2.46972e-05 | 0.00351397 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439386 | CAGGCCCATGACCTG[A/T]TTGAGGAGGCTGCTC | 899 |
rs770069823 | in-del | -/CCCCTCCATCCCCTCCAC | 1.66838e-05 | 0.00288818 | intron-variant | CCNF | GRCh38.p7 | 16:2449795 | CTCCGTCCCCTCCAT[-/CCCCTCCATCCCCTCCAC]CCCCTCCACCCCTGG | 899 |
rs770169292 | snp | C/G/T | 3.30881e-05 | 0.00406733 | stop-gained, missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456836 | TGCCCCAACCTACCT[C/G/T]AGTGCTGTCCCTGGA | 899 |
rs770256445 | snp | A/G | 1.64811e-05 | 0.00287059 | intron-variant | CCNF | GRCh38.p7 | 16:2438133 | TTCGAGGTGAGTCAA[A/G]TTGTTCTCTGCACTG | 899 |
rs770289699 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2440052 | ATCTCTGCCTATCCA[C/T]TCTTGCCTCTCAGCC | 899 |
rs770353839 | snp | C/T | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457096 | AGCATAGCATAGGAA[C/T]GCTGCATAGACCATG | 899 |
rs770372021 | snp | C/T | 1.65356e-05 | 0.00287533 | intron-variant | CCNF | GRCh38.p7 | 16:2435894 | TCCTCACCCCACCTG[C/T]ATGTTGGCGCTTCAG | 899 |
rs770399989 | snp | C/T | 3.30994e-05 | 0.004068 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445571 | GGAGGAGGCTGGTGC[C/T]GCGGTACAGGCTCCA | 899 |
rs770412291 | snp | A/C | 1.64931e-05 | 0.00287163 | intron-variant | CCNF | GRCh38.p7 | 16:2449815 | TCCACCCCTGGCCTG[A/C]TTTCCTCCCCAGCAC | 899 |
rs770482472 | snp | A/G | 1.65323e-05 | 0.00287505 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2435806 | TTCTTAATGTTTCAG[A/G]GCTGCTGAAAAGGGG | 899 |
rs770498667 | snp | C/T | 1.64754e-05 | 0.00287009 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443740 | AGCTATTTCAGGCTT[C/T]CCAGGCTGTCAGTAA | 899 |
rs770543533 | in-del | -/AGG | 1.79574e-05 | 0.00299639 | cds-indel | CCNF | GRCh38.p7 | 16:2455466 | CGGAGCTGTCCAGCC[-/AGG]AGGAGACGCTGCTGG | 899 |
rs770551533 | snp | C/T | 1.65696e-05 | 0.00287828 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443619 | AACATGGCTGCTGTC[C/T]CACGCTCATGTTTGT | 899 |
rs770610264 | snp | C/T | 0.000242292 | 0.011004 | intron-variant | CCNF | GRCh38.p7 | 16:2455355 | GCCTCCCAGCGCCGC[C/T]GTCCATGACTGGGTC | 899 |
rs770688819 | snp | A/G | 1.66499e-05 | 0.00288525 | intron-variant | CCNF | GRCh38.p7 | 16:2453579 | CCATACAATGCTGGC[A/G]TCCTCGTGCCGGCCC | 899 |
rs770698408 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434586 | ACTGCACTCCAGCCT[A/G]AGCAACAGAGCGAGA | 899 |
rs770722561 | snp | A/G | 2.04849e-05 | 0.00320032 | intron-variant | CCNF | GRCh38.p7 | 16:2449089 | TGGACTCAGAGAGCA[A/G]CTGTCTCTGCTGTGC | 899 |
rs770751518 | snp | A/C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2433314 | GCCCGTGGTGCCTCC[A/C/G]GAGGGCTGTGATCCA | 899 |
rs770775588 | snp | A/T | 1.65258e-05 | 0.00287448 | missense | CCNF | GRCh38.p7 | 16:2453293 | ACAAGCGCTATGGAG[A/T]AATCAGCCAGGAAGA | 899 |
rs770868945 | snp | A/C | 6.62186e-05 | 0.00575369 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445502 | TTGCCACCATGAAGG[A/C]CTTCACAAGCCTGTG | 899 |
rs770988688 | snp | A/G | 1.67211e-05 | 0.00289142 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456722 | CCAAACCCCTGGTCC[A/G]CACCAGCCGGGAGCC | 899 |
rs770996337 | snp | C/T | 1.65597e-05 | 0.00287743 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437219 | TGAATGTGGGTGCCG[C/T]ACCTTTCATCTGGCT | 899 |
rs771041686 | snp | A/G | 1.68618e-05 | 0.00290356 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456647 | CTTGTCCAGAGGACA[A/G]GGGACCCCAGGACCC | 899 |
rs771130093 | snp | A/G | 6.66422e-05 | 0.00577206 | missense | CCNF | GRCh38.p7 | 16:2449306 | GTGGTGGATTACAAG[A/G]AGGTCCTGCTGACGC | 899 |
rs771132756 | snp | G/T | 1.64749e-05 | 0.00287005 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431255 | ATCCTGAAATGGCTT[G/T]CTGTAGAGGACATCC | 899 |
rs771185292 | snp | C/G | 1.65729e-05 | 0.00287857 | intron-variant | CCNF | GRCh38.p7 | 16:2453542 | AGAACCAAACGGTTA[C/G]TTACCCTGCGTTCTG | 899 |
rs771206972 | snp | A/G | 0.000183802 | 0.00958475 | intron-variant | CCNF | GRCh38.p7 | 16:2432949 | CCAGCCCCGGCCCCC[A/G]TTGTTCTGCAGGTAC | 899 |
rs771290658 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438299 | CCTGGCCACGGGCTC[C/T]GATCCTGGCTCCATG | 899 |
rs771307969 | snp | A/G | 3.30628e-05 | 0.00406575 | missense | CCNF | GRCh38.p7 | 16:2453482 | CCCCCGACTTTCCTC[A/G]GCACAGGGGAGATCC | 899 |
rs771392264 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2439155 | ATACAAAAATTAGCC[A/G]GGCATGATGGTGGGC | 899 |
rs771457669 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2456069 | AGGAGGCTGAGGTGG[A/G]AGGATCTCTTGAGCA | 899 |
rs771491431 | snp | C/G | 3.17425e-05 | 0.00398375 | intron-variant | CCNF | GRCh38.p7 | 16:2439493 | GTCGGGGGGAGTTAT[C/G]CTGGACAAAGGCGTA | 899 |
rs771496661 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | CCNF | GRCh38.p7 | 16:2449840 | CAGCACAGCCCTGGA[C/T]CACTCAGCTGTGGGA | 899 |
rs771512791 | in-del | -/ATATATATATATATATAT | | | intron-variant | CCNF | GRCh38.p7 | 16:2435667 | TATGCACACACACAC[-/ATATATATATATATATAT]ATATATATATATATA | 899 |
rs771544471 | snp | C/T | 6.46517e-05 | 0.00568521 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439414 | CTCATCAGGGATGTC[C/T]GACCAGCTCCTACCT | 899 |
rs771586274 | in-del | -/GT | 1.76899e-05 | 0.00297399 | intron-variant | CCNF | GRCh38.p7 | 16:2455569 | GGAGGGCGACGGTGA[-/GT]GTGGGGCCAGGGTGC | 899 |
rs771621178 | snp | A/G | | | missense | CCNF | GRCh38.p7 | 16:2455549 | CAGGAGAGTGAGGGC[A/G]AGAAGGAGGGCGACG | 899 |
rs771669249 | snp | A/G | 1.6717e-05 | 0.00289106 | intron-variant | CCNF | GRCh38.p7 | 16:2448820 | CCTGCCCCAGGAAGT[A/G]GGCTCCACCCTGAGA | 899 |
rs771737804 | in-del | -/ACCC | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428042 | AAGTAGGAAACAGTA[-/ACCC]AGGAGGACAAAAGTG | 899 |
rs771852887 | snp | C/G | 1.64795e-05 | 0.00287045 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443760 | GCTGTCAGTAAACAA[C/G]AAGTCTTCTCCGTGC | 899 |
rs771891105 | snp | C/G | 2.07751e-05 | 0.00322291 | intron-variant | CCNF | GRCh38.p7 | 16:2449106 | TGTCTCTGCTGTGCC[C/G]AAAGCCATGGAGCAG | 899 |
rs771908083 | snp | A/G | 3.84342e-05 | 0.00438356 | intron-variant | CCNF | GRCh38.p7 | 16:2449168 | GCTGGTGCGCTACGC[A/G]TGCAGCATCGGCGTG | 899 |
rs771912720 | snp | G/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445271 | GTGGGGCCTGCTTTG[G/T]GGCTGGGACCCACGG | 899 |
rs772045018 | in-del | -/T | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457545 | CCTTCTGGGTGGGGC[-/T]TCCATGGTAAGGGGG | 899 |
rs772064770 | in-del | -/TG | 4.98931e-05 | 0.00499441 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443601 | TCAGAAATGGAAAAC[-/TG]CAACATGGCTGCTGT | 899 |
rs772080724 | snp | A/C | 3.29804e-05 | 0.00406068 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2438075 | TTTTTTAAAGACTCA[A/C]AAAGCATCCATATTG | 899 |
rs772127041 | snp | C/G | 1.6574e-05 | 0.00287867 | intron-variant | CCNF | GRCh38.p7 | 16:2453380 | TCACCCTCGGGGCCT[C/G]TGCACCCCCTAACTC | 899 |
rs772147128 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428357 | TATGGGGACCCGGAA[A/G]GATGGAAGGGTGCAG | 899 |
rs772150233 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441177 | AGGAGGAAGTTGCAG[C/T]GAGCCGAGATTGTGC | 899 |
rs772180279 | snp | C/T | 1.65446e-05 | 0.00287612 | intron-variant | CCNF | GRCh38.p7 | 16:2453320 | AAGAGGTGCCTCCCT[C/T]CCGCCACCTGGGCGT | 899 |
rs772182362 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2434345 | TATGGCTGGGCACAG[G/T]GGCTCACGCCTGTAA | 899 |
rs772205153 | snp | A/G | 6.60917e-05 | 0.00574817 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445556 | TGGACCGGTACCTGC[A/G]GAGGAGGCTGGTGCC | 899 |
rs772207315 | snp | A/G | 0.000268702 | 0.0115879 | intron-variant | CCNF | GRCh38.p7 | 16:2437325 | CCAGCTGCAGAGGGT[A/G]AGTCTGGGCGAGGGG | 899 |
rs772229861 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2436317 | CAGGCAGGTTAGAAC[C/T]GGCCTGGTGCCTGGA | 899 |
rs772260732 | snp | C/T | 3.31554e-05 | 0.00407144 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445505 | CCACCATGAAGGACT[C/T]CACAAGCCTGTGCCT | 899 |
rs772287531 | snp | A/G | 1.6912e-05 | 0.00290787 | missense | CCNF | GRCh38.p7 | 16:2449391 | CCCTGCTGCACACCA[A/G]CCTGTCCGCCTACGC | 899 |
rs772326715 | snp | A/G | 6.70387e-05 | 0.0057892 | intron-variant | CCNF | GRCh38.p7 | 16:2449249 | AAGGAGCCCCCGAGC[A/G]CTGAGAGCCCACACC | 899 |
rs772355945 | snp | C/G | 1.67452e-05 | 0.0028935 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456670 | CAGGACCCACAGGCA[C/G]TGGCGCTGGACACCC | 899 |
rs772431415 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2450908 | TGCTGGGATAGAGCT[A/G]TCCTCTGTCTCACTG | 899 |
rs772442115 | snp | C/T | 6.67011e-05 | 0.00577461 | missense | CCNF | GRCh38.p7 | 16:2449319 | AGGAGGTCCTGCTGA[C/T]GCTAGTCCCTGTGGA | 899 |
rs772479219 | snp | A/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459338 | GTTAACACCAACTAC[A/G]TGGGGCCCTGCTGCC | 899 |
rs772604305 | in-del | -/TT | 0.000169466 | 0.00920348 | intron-variant | CCNF | GRCh38.p7 | 16:2431010 | TCTTTTGTGGCACAG[-/TT]GGAATAGTAACCATT | 899 |
rs772632798 | snp | A/C | 1.97381e-05 | 0.00314144 | intron-variant, missense | CCNF | GRCh38.p7 | 16:2432966 | TGTTCTGCAGGTACA[A/C]TCCCAGCTGAAGGAC | 899 |
rs772751358 | snp | C/T | 2.2965e-05 | 0.00338851 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457027 | AGGCTGTAAGTGTGT[C/T]AGCACATTTGCCGCA | 899 |
rs772753529 | snp | C/T | 3.33695e-05 | 0.00408456 | missense | CCNF | GRCh38.p7 | 16:2449328 | TGCTGACGCTAGTCC[C/T]TGTGGAGCTGAGAAC | 899 |
rs772769046 | in-del | -/CTGCGG | 1.65113e-05 | 0.00287322 | cds-indel, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445552 | TGTGTGGACCGGTAC[-/CTGCGG]AGGAGGCTGGTGCCG | 899 |
rs772780796 | snp | C/T | 3.33784e-05 | 0.0040851 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2439799 | AAAACTCAGGGACTA[C/T]GCTGCCAAAGGCTGC | 899 |
rs772817268 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2456109 | GGAGCTGCAGTGAGC[C/T]GTGATCATGCCACTG | 899 |
rs772822770 | snp | C/T | 9.27543e-05 | 0.00680945 | intron-variant | CCNF | GRCh38.p7 | 16:2455352 | CTGGCCTCCCAGCGC[C/T]GCCGTCCATGACTGG | 899 |
rs772850532 | snp | A/G | 1.65633e-05 | 0.00287774 | intron-variant | CCNF | GRCh38.p7 | 16:2453202 | ACTCCACGTGACTCT[A/G]TTTCCAGCTTCCATG | 899 |
rs772856097 | in-del | -/CCCTCCATT | 3.30644e-05 | 0.00406585 | intron-variant | CCNF | GRCh38.p7 | 16:2449796 | TCCGTCCCCTCCATC[-/CCCTCCATT]CCCTCCACCCCTGGC | 899 |
rs772904662 | snp | C/T | 1.65315e-05 | 0.00287498 | intron-variant | CCNF | GRCh38.p7 | 16:2449004 | GTTCCATTTTCCTTA[C/T]TAATCTTCGTTGTCG | 899 |
rs772905902 | snp | C/G/T | 5.43093e-05 | 0.00521078 | intron-variant | CCNF | GRCh38.p7 | 16:2439713 | GTTCCTCCCAAGACA[C/G/T]AGTTGTACAAAGGCT | 899 |
rs772955914 | snp | C/G/T | 3.3193e-05 | 0.00407377 | intron-variant | CCNF | GRCh38.p7 | 16:2453555 | TAGTTACCCTGCGTT[C/G/T]TGGCTGCGCCATACA | 899 |
rs773048566 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2432826 | ACTTTCACACAGAGA[C/T]TGGGGACCTCAACTA | 899 |
rs773143511 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2452491 | GCTGTTTCTGGGCTG[C/T]GTTTATTCTCTTCCT | 899 |
rs773151435 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | CCNF | GRCh38.p7 | 16:2449933 | GAGTTTTGGCCGGGC[A/G]CAGAGGCTCATGCCT | 899 |
rs773191475 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428396 | AAGCGTGAGGGAGGG[A/G]TGGGCAGCCTTGGCC | 899 |
rs773248714 | snp | A/C/T | 0.00031966 | 0.0126391 | intron-variant | CCNF | GRCh38.p7 | 16:2449241 | ACTGCACCAAGGAGC[A/C/T]CCCGAGCGCTGAGAG | 899 |
rs773313297 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2430019 | TTATCATAGTATCTG[C/T]CCTGGAGCCGGAGAA | 899 |
rs773318963 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2451211 | GTCGTGACGAGAGAA[A/G]CAGCAGGCAGGCGCG | 899 |
rs773326682 | snp | A/G | 1.69006e-05 | 0.00290689 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437152 | TCTGATGAGGCCCGC[A/G]CAGAAGTGAATGGCC | 899 |
rs773421567 | snp | A/G | 1.65048e-05 | 0.00287265 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443791 | AGAAGGGACTCAATG[A/G]CACAATGAGGTGAGG | 899 |
rs773496722 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2450909 | GCTGGGATAGAGCTA[C/T]CCTCTGTCTCACTGA | 899 |
rs773521452 | snp | A/C/G | 6.58917e-05 | 0.00573952 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431151 | ACTGTAGGTGTGCCA[A/C/G]GTGTTTCTGTTATCC | 899 |
rs773540858 | snp | A/G | 1.65493e-05 | 0.00287652 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453415 | TTCCCCTCAGGTGCT[A/G]AGCTACAGCCAGTTG | 899 |
rs773548489 | snp | A/C | 1.80748e-05 | 0.00300618 | intron-variant | CCNF | GRCh38.p7 | 16:2449186 | CAGCATCGGCGTGAA[A/C]ATCATCCGGGCCAGA | 899 |
rs773672931 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2436865 | AGCGTCGCGGGGTCT[C/T]CTTCCCCTGACCTTC | 899 |
rs773853996 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440054 | CTCTGCCTATCCACT[C/G]TTGCCTCTCAGCCAG | 899 |
rs773872217 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2438516 | CGTGGTGGCGGGTGC[C/G]CATAATCCCAGCTAC | 899 |
rs773879045 | snp | A/G | 9.04227e-05 | 0.00672333 | intron-variant | CCNF | GRCh38.p7 | 16:2455356 | CCTCCCAGCGCCGCC[A/G]TCCATGACTGGGTCT | 899 |
rs773925421 | snp | A/G | 4.96611e-05 | 0.00498278 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445572 | GAGGAGGCTGGTGCC[A/G]CGGTACAGGCTCCAG | 899 |
rs773933025 | snp | C/G | 1.65312e-05 | 0.00287495 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2435808 | CTTAATGTTTCAGGG[C/G]TGCTGAAAAGGGGAA | 899 |
rs774028397 | in-del | -/GAGAGTGAGGGC | 1.72397e-05 | 0.00293591 | cds-indel | CCNF | GRCh38.p7 | 16:2455537 | TATGAAGGCGACCAG[-/GAGAGTGAGGGC]GAGAAGGAGGGCGAC | 899 |
rs774051087 | snp | C/T | 1.6566e-05 | 0.00287797 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443620 | ACATGGCTGCTGTCT[C/T]ACGCTCATGTTTGTC | 899 |
rs774053229 | snp | G/T | 1.84613e-05 | 0.00303814 | intron-variant, synonymous-codon | CCNF | GRCh38.p7 | 16:2433032 | CAGCTTCCAGGAGCT[G/T]TGGCCGTCTCCAGGG | 899 |
rs774062677 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2430372 | GGGGTTGCTGGAGTA[A/G]GAGTTGGAAAATCCG | 899 |
rs774096632 | snp | G/T | 6.81118e-05 | 0.00583534 | missense | CCNF | GRCh38.p7 | 16:2449411 | TCCGCCTACGCCCCA[G/T]CCCGCCTGGCTGCCG | 899 |
rs774144745 | snp | A/T | | | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447296 | TTTTTTTTTTTTTAA[A/T]TCCGGGGACCAGGCA | 899 |
rs774245832 | snp | A/G | | | missense | CCNF | GRCh38.p7 | 16:2448859 | CGGCGTTGCAGGTTT[A/G]TCAGTAAAGAGATCC | 899 |
rs774298900 | snp | C/T | 3.32535e-05 | 0.00407746 | intron-variant | CCNF | GRCh38.p7 | 16:2449012 | TTCCTTATTAATCTT[C/T]GTTGTCGCTGTGCTG | 899 |
rs774328320 | snp | A/C | 4.96923e-05 | 0.00498434 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437220 | GAATGTGGGTGCCGC[A/C]CCTTTCATCTGGCTC | 899 |
rs774336176 | snp | C/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445226 | TCAAAGCGCTTGTGT[C/T]TGGGAGCACCAGGAA | 899 |
rs774339016 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2439727 | ACAGTTGTACAAAGG[C/G]TCGGTGATCTCCCAT | 899 |
rs774397102 | snp | C/G | 4.1165e-05 | 0.00453661 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437307 | GAGCCTCAGGGCAGA[C/G]TGCCAGCTGCAGAGG | 899 |
rs774453479 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2430927 | TTTGAAAATGAATGA[C/T]CTCTTCTGTAATTTG | 899 |
rs774480830 | in-del | -/TTTG | 6.82652e-05 | 0.00584191 | intron-variant | CCNF | GRCh38.p7 | 16:2430968 | CTCCTTTACATAATC[-/TTTG]TTTGGGACAAGAAGC | 899 |
rs774560881 | snp | A/G | 3.37046e-05 | 0.00410502 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456648 | TTGTCCAGAGGACAA[A/G]GGACCCCAGGACCCA | 899 |
rs774562546 | snp | A/G | 1.7159e-05 | 0.00292903 | intron-variant | CCNF | GRCh38.p7 | 16:2449208 | CGGGCCAGACCCTGC[A/G]CTGGGCCTGCATGCG | 899 |
rs774622969 | snp | A/G | 1.66668e-05 | 0.00288672 | missense | CCNF | GRCh38.p7 | 16:2449309 | GTGGATTACAAGGAG[A/G]TCCTGCTGACGCTAG | 899 |
rs774705289 | snp | C/T | 1.65611e-05 | 0.00287755 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445344 | TCCAGGGTAAACCCA[C/T]GATTCCAGAGCTAGC | 899 |
rs774732292 | snp | A/C | 1.66682e-05 | 0.00288684 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456940 | CCGGAGAGCAGTGTT[A/C]CCCAGCAACAGGTGA | 899 |
rs774772235 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2436643 | TCAAAGAGCAGTTCC[C/G]AGACATAAAATTCAC | 899 |
rs774802568 | snp | G/T | 4.9597e-05 | 0.00497956 | missense | CCNF | GRCh38.p7 | 16:2453489 | CTTTCCTCAGCACAG[G/T]GGAGATCCACGCCTT | 899 |
rs774815615 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2448484 | TAATCAAAGCTCACT[A/G]CAGCCTCAACTTCCT | 899 |
rs774887919 | snp | C/T | 1.64754e-05 | 0.00287009 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2431257 | CCTGAAATGGCTTTC[C/T]GTAGAGGACATCCTG | 899 |
rs774939405 | snp | A/G | 3.29462e-05 | 0.00405857 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2431170 | TTTCTGTTATCCTAC[A/G]AAGCGAAGAATAAGG | 899 |
rs774965525 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454317 | CAGCACTTTCCATTG[A/T]GTGGAAGGCAGGAGA | 899 |
rs775034470 | snp | G/T | 3.29484e-05 | 0.00405871 | intron-variant | CCNF | GRCh38.p7 | 16:2448822 | TGCCCCAGGAAGTGG[G/T]CTCCACCCTGAGACC | 899 |
rs775054989 | snp | A/G | 1.67033e-05 | 0.00288987 | intron-variant | CCNF | GRCh38.p7 | 16:2435903 | CACCTGCATGTTGGC[A/G]CTTCAGATAAGTGTG | 899 |
rs775057877 | snp | C/T | 2.14562e-05 | 0.00327531 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439422 | GGATGTCTGACCAGC[C/T]CCTACCTCCTCTGGG | 899 |
rs775130027 | snp | A/C/G | 3.4895e-05 | 0.0041769 | missense | CCNF | GRCh38.p7 | 16:2455556 | GTGAGGGCGAGAAGG[A/C/G]GGGCGACGGTGAGTG | 899 |
rs775163061 | snp | C/T | 4.94238e-05 | 0.00497086 | missense | CCNF | GRCh38.p7 | 16:2449857 | ACTCAGCTGTGGGAC[C/T]TCACCGGATTCTCCT | 899 |
rs775376235 | snp | A/T | 1.65121e-05 | 0.00287329 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2435833 | GGGGAATTTCGAAGC[A/T]GCTGTGAAGCTGGGC | 899 |
rs775408780 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2455222 | CTCCAGGTTGGCCCT[G/T]CCTGAAGGGCTTATA | 899 |
rs775427467 | in-del | -/GAG | 1.71543e-05 | 0.00292862 | cds-indel, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456625 | CAGGAATCCAGTGAT[-/GAG]GAGGCTTGTCCAGAG | 899 |
rs775441275 | snp | A/C | 4.95692e-05 | 0.00497816 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443627 | TGCTGTCTCACGCTC[A/C]TGTTTGTCTTTTCTT | 899 |
rs775549664 | snp | A/T | 1.70041e-05 | 0.00291577 | intron-variant | CCNF | GRCh38.p7 | 16:2430995 | AAGAAGCATAGTTCC[A/T]TCTTTTGTGGCACAG | 899 |
rs775567104 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2450877 | CTTGAGAGAACAGCT[G/T]CTGCCCTGATGCAGC | 899 |
rs775622915 | snp | C/T | 2.47724e-05 | 0.00351932 | intron-variant | CCNF | GRCh38.p7 | 16:2437329 | CTGCAGAGGGTGAGT[C/T]TGGGCGAGGGGCAGC | 899 |
rs775623319 | snp | A/G | 1.65255e-05 | 0.00287445 | missense | CCNF | GRCh38.p7 | 16:2453284 | GGTTTGAGGACAAGC[A/G]CTATGGAGAAATCAG | 899 |
rs775693958 | snp | C/T | 3.31022e-05 | 0.00406817 | intron-variant | CCNF | GRCh38.p7 | 16:2453322 | GAGGTGCCTCCCTCC[C/T]GCCACCTGGGCGTCT | 899 |
rs775700771 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2436549 | ACCTGGCCGGCTGGC[A/G]GAATTGTGACTGACA | 899 |
rs775708444 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2438384 | AGGCATCGAACCTCG[A/C]TGCTCACTCGTCTGC | 899 |
rs775745699 | snp | A/C | 1.65712e-05 | 0.00287843 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445506 | CACCATGAAGGACTT[A/C]ACAAGCCTGTGCCTG | 899 |
rs775747522 | snp | C/G | 3.32646e-05 | 0.00407814 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437235 | ACCTTTCATCTGGCT[C/G]TTCATCCGCCCTCCG | 899 |
rs775797148 | snp | C/T | 1.67421e-05 | 0.00289323 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456671 | AGGACCCACAGGCAC[C/T]GGCGCTGGACACCCA | 899 |
rs775797896 | in-del | -/AT | | | intron-variant | CCNF | GRCh38.p7 | 16:2434954 | TTCGTATTTGATTAC[-/AT]GTTATTAAGAAATGT | 899 |
rs775814110 | snp | A/C/G | 3.33557e-05 | 0.00408374 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449320 | GGAGGTCCTGCTGAC[A/C/G]CTAGTCCCTGTGGAG | 899 |
rs775818588 | snp | C/G | 1.65318e-05 | 0.002875 | missense | CCNF | GRCh38.p7 | 16:2453244 | AAGGACTACAGGCAA[C/G]TCTCTCTGACCGCCG | 899 |
rs775823299 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458161 | GCCTCTCCCTGGGAA[C/T]GGGCTGACCACAACA | 899 |
rs775869425 | snp | A/G | 1.6582e-05 | 0.00287936 | intron-variant | CCNF | GRCh38.p7 | 16:2453550 | ACGGTTAGTTACCCT[A/G]CGTTCTGGCTGCGCC | 899 |
rs775895715 | in-del | -/T | 0.00127984 | 0.0252643 | intron-variant | CCNF | GRCh38.p7 | 16:2431054 | ATGTAACTTTTATCC[-/T]TTTTTTTTCCCTTCA | 899 |
rs775908273 | snp | A/T | 0.000150629 | 0.00867708 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2439766 | GTCAGATCCTGGGCG[A/T]TGCCTCCACAGCTTC | 899 |
rs776106564 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2438177 | ATACATCCCTAGCCG[-/A]AGATCCTGGAACTGA | 899 |
rs776129398 | snp | C/G | 1.91298e-05 | 0.00309266 | intron-variant, missense | CCNF | GRCh38.p7 | 16:2432972 | GCAGGTACACTCCCA[C/G]CTGAAGGACCTGGTG | 899 |
rs776205765 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433380 | GGAAACTTCACTCAG[C/T]CTTCCTTCCCTTTGG | 899 |
rs776257057 | snp | G/T | | | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446930 | TCTTCGGGCCTGTGT[G/T]TGCCAGCTCGATGCA | 899 |
rs776266517 | in-del | -/ACCTACCTCAGTGCTGTCCCT | 1.81447e-05 | 0.00301198 | cds-indel, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456989 | ACACAGTGAGGAGGA[-/ACCTACCTCAGTGCTGTCCCT]GGACATGAACCTGGG | 899 |
rs776287774 | snp | A/G | 3.29679e-05 | 0.00405991 | missense | CCNF | GRCh38.p7 | 16:2448892 | ACCATCCGGGAGGCC[A/G]TATGGCTCACGGACA | 899 |
rs776348562 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2441077 | TCTTTACTAAAAATA[C/G]AAAAAAATTAGCTGG | 899 |
rs776351633 | in-del | -/C | 1.66513e-05 | 0.00288537 | intron-variant | CCNF | GRCh38.p7 | 16:2431063 | TTATCCTTTTTTTTT[-/C]CCTTCAAGGGTGTGT | 899 |
rs776384745 | snp | A/G | 5.02904e-05 | 0.00501425 | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456507 | TCCCCTGATGCTTGG[A/G]TGTGACATGACTTCC | 899 |
rs776384962 | snp | A/G | 4.94238e-05 | 0.00497086 | missense | CCNF | GRCh38.p7 | 16:2449863 | CTGTGGGACCTCACC[A/G]GATTCTCCTATGAAG | 899 |
rs776563616 | snp | A/C/G | 3.57528e-05 | 0.00422792 | intron-variant | CCNF | GRCh38.p7 | 16:2437084 | AGCTTTCCACATTCC[A/C/G]TCCCTAAGAGACATC | 899 |
rs776665495 | snp | C/T | 1.65586e-05 | 0.00287733 | intron-variant | CCNF | GRCh38.p7 | 16:2453403 | CCTAACTCTAGCTTC[C/T]CCTCAGGTGCTGAGC | 899 |
rs776723050 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428509 | TGTGCCGTAAAAGGG[A/G]TGCGGTGTGGCTGAC | 899 |
rs776766249 | snp | C/T | 1.64966e-05 | 0.00287194 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443785 | CCGTGCAGAAGGGAC[C/T]CAATGACACAATGAG | 899 |
rs776824044 | snp | A/C | 5.05157e-05 | 0.00502546 | intron-variant | CCNF | GRCh38.p7 | 16:2431030 | TAGTAACCATTAGAT[A/C]ATCTTCAGATGTAAC | 899 |
rs776914139 | snp | A/G | 1.65625e-05 | 0.00287766 | intron-variant | CCNF | GRCh38.p7 | 16:2453334 | TCCCGCCACCTGGGC[A/G]TCTCATGGGGTGCTG | 899 |
rs776942468 | snp | A/G | 2.07743e-05 | 0.00322284 | intron-variant | CCNF | GRCh38.p7 | 16:2449134 | CAGGAGGCCACGGTT[A/G]CACCACGTCGCCATC | 899 |
rs776944118 | snp | A/G | 1.6504e-05 | 0.00287258 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445515 | GGACTTCACAAGCCT[A/G]TGCCTGCACCTGACC | 899 |
rs776957393 | snp | C/T | 6.59294e-05 | 0.00574111 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2438091 | AAAGCATCCATATTG[C/T]ACTGCTTGGGCAGAG | 899 |
rs777019340 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2456206 | CCTCACTGCCCTGCT[A/G]GGATCACTGCCCTGT | 899 |
rs777040047 | snp | A/G | 1.66222e-05 | 0.00288285 | intron-variant | CCNF | GRCh38.p7 | 16:2435783 | ATAAAATATTGTGAT[A/G]CTTTATGTTCTTAAT | 899 |
rs777081653 | snp | C/G | 6.6143e-05 | 0.0057504 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445563 | GTACCTGCGGAGGAG[C/G]CTGGTGCCGCGGTAC | 899 |
rs777084475 | snp | A/G | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457149 | AGAGGATGACTTGCG[A/G]CCACCAAGTTTCTGT | 899 |
rs777122266 | in-del | -/AAC | 4.94311e-05 | 0.00497123 | cds-indel, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443755 | CCCAGGCTGTCAGTA[-/AAC]AACAAGTCTTCTCCG | 899 |
rs777132064 | snp | C/T | 2.52146e-05 | 0.00355059 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457039 | TGTCAGCACATTTGC[C/T]GCAGTGGATGTGTAC | 899 |
rs777158941 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438340 | CAGGGGAGTGGGGGA[C/T]GGTGAGAACAGCAGA | 899 |
rs777183197 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2439062 | CAGCACTTTGGGAGA[C/T]TGAGGTGGGTGGATC | 899 |
rs777297170 | snp | A/G | 1.99499e-05 | 0.00315825 | intron-variant | CCNF | GRCh38.p7 | 16:2449157 | TCGCCATCTGCGCTG[A/G]TGCGCTACGCGTGCA | 899 |
rs777337900 | snp | C/T | 1.94831e-05 | 0.00312109 | intron-variant | CCNF | GRCh38.p7 | 16:2449074 | TGTGGGAGGGCCTCA[C/T]GGACTCAGAGAGCAG | 899 |
rs777340745 | snp | C/T | 0.000102034 | 0.00714189 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449404 | CAGCCTGTCCGCCTA[C/T]GCCCCAGCCCGCCTG | 899 |
rs777399828 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2448741 | TGTTTGTCACCAAAG[C/G]CCAACGCCATGGCTC | 899 |
rs777415748 | snp | A/C | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457874 | ATGCCATCCTGACAC[A/C]CTTTATGCAAAAAGA | 899 |
rs777452114 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458641 | TGTGTGTTCATGTCC[A/G]CGGCAGCTGTCTTTT | 899 |
rs777509490 | snp | C/T | 1.65482e-05 | 0.00287643 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445491 | GCTGGTGGAAGTTGC[C/T]ACCATGAAGGACTTC | 899 |
rs777513820 | in-del | -/GCACAC | | | intron-variant | CCNF | GRCh38.p7 | 16:2435678 | CACATATATATATAT[-/GCACAC]ATATATATATATATA | 899 |
rs777521800 | snp | C/G | 1.70525e-05 | 0.00291992 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456630 | ATCCAGTGATGAGGA[C/G]GCTTGTCCAGAGGAC | 899 |
rs777550770 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427679 | AGCCCAGTGGGAAAC[A/G]GGCCCACACCCTGGA | 899 |
rs777566113 | in-del | -/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2430271 | GGTAGATTTGTAGAT[-/G]GGGAGGCAGGATCCT | 899 |
rs777593699 | snp | C/G | 1.67133e-05 | 0.00289074 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456720 | ACCCAAACCCCTGGT[C/G]CGCACCAGCCGGGAG | 899 |
rs777630156 | snp | C/T | 1.6855e-05 | 0.00290297 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449381 | TGCGAGCTCTCCCTG[C/T]TGCACACCAGCCTGT | 899 |
rs777646899 | snp | A/G | 8.25185e-05 | 0.0064228 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445535 | TGCACCTGACCGTGG[A/G]GTGTGTGGACCGGTA | 899 |
rs777682489 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434461 | CTACTAAAAATACAA[A/G]AATTAGCTGGGTGGT | 899 |
rs777735346 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2448019 | GGGGAAGGTGCCTTG[C/T]GGGGGGCCGCTGGAG | 899 |
rs777735624 | snp | A/C | 5.6878e-05 | 0.00533252 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437293 | GCCGTGGTTCACGAG[A/C]GCCTCAGGGCAGAGT | 899 |
rs777762783 | in-del | -/AGA | 0.000277241 | 0.0117705 | cds-indel | CCNF | GRCh38.p7 | 16:2455550 | AGGAGAGTGAGGGCG[-/AGA]AGGAGGGCGACGGTG | 899 |
rs777803431 | snp | C/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445119 | CTGTCCACCTTCTCC[C/T]GCTCCCTGCACGCCC | 899 |
rs777842545 | snp | C/T | 1.64732e-05 | 0.0028699 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2431233 | CCCCGAAGATGTGCT[C/T]TTTCACATCCTGAAA | 899 |
rs777880085 | snp | A/G | 1.66618e-05 | 0.00288628 | missense | CCNF | GRCh38.p7 | 16:2449291 | GTCTAGGTCCCCACT[A/G]TGGTGGATTACAAGG | 899 |
rs777908743 | snp | A/G | 5.98964e-05 | 0.00547217 | intron-variant | CCNF | GRCh38.p7 | 16:2439488 | TCTGGGTCGGGGGGA[A/G]TTATGCTGGACAAAG | 899 |
rs777911744 | snp | A/C | 5.00826e-05 | 0.00500388 | intron-variant | CCNF | GRCh38.p7 | 16:2432944 | ATCACCCAGCCCCGG[A/C]CCCCGTTGTTCTGCA | 899 |
rs777932158 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2455657 | CCCTGTGCGAGCGCT[G/T]TGGGAGGAAGATGTG | 899 |
rs777975543 | snp | A/G | 3.9703e-05 | 0.00445533 | missense, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457004 | AGGACATGAACCTGG[A/G]CCTTGTGAGGCTGTA | 899 |
rs777986464 | in-del | -/G | 0.000284544 | 0.0119244 | intron-variant | CCNF | GRCh38.p7 | 16:2455350 | GCCTGGCCTCCCAGC[-/G]CCGCCGTCCATGACT | 899 |
rs778054573 | snp | C/T | 1.71929e-05 | 0.00293192 | intron-variant | CCNF | GRCh38.p7 | 16:2439740 | GGCTCGGTGATCTCC[C/T]ATTGACAGGTGTCAG | 899 |
rs778090367 | snp | A/T | 3.30846e-05 | 0.00406709 | synonymous-codon, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456918 | ACAGTGTCGTCCCCC[A/T]AGTCCCCCGGAGAGC | 899 |
rs778239846 | snp | C/T | 1.65416e-05 | 0.00287586 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437185 | AAGGCCTCTCGCTTC[C/T]TCAGTCTCGCTGAGC | 899 |
rs778264897 | snp | A/G | 1.72585e-05 | 0.00293751 | missense | CCNF | GRCh38.p7 | 16:2455540 | GAAGGCGACCAGGAG[A/G]GTGAGGGCGAGAAGG | 899 |
rs778293068 | snp | C/T | 0.000366214 | 0.0135267 | intron-variant | CCNF | GRCh38.p7 | 16:2437124 | TGTCCTGTCTGTCCC[C/T]GCAGTGTCTGTGTCT | 899 |
rs778360498 | snp | A/C/G | 4.94648e-05 | 0.00497296 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2438077 | TTTTAAAGACTCACA[A/C/G]AGCATCCATATTGCA | 899 |
rs778366820 | snp | C/G/T | 3.39762e-05 | 0.00412155 | intron-variant | CCNF | GRCh38.p7 | 16:2449220 | TGCGCTGGGCCTGCA[C/G/T]GCGGCACTGCACCAA | 899 |
rs778367970 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452836 | TTCCCTCGCGGTAAC[A/G]TTTGCTGGGTTTGTC | 899 |
rs778367996 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449898 | CATTCCCTGCGTCTT[A/G]AGCCTCCATAAGAAG | 899 |
rs778412673 | snp | A/C/G | 3.77289e-05 | 0.00434319 | intron-variant | CCNF | GRCh38.p7 | 16:2455606 | AAGGGACATCACACA[A/C/G]AGGGTGGCTCTCACC | 899 |
rs778470923 | snp | C/G | 1.6476e-05 | 0.00287014 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443745 | TTTCAGGCTTCCCAG[C/G]CTGTCAGTAAACAAC | 899 |
rs778492647 | snp | A/C | 1.64789e-05 | 0.0028704 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449835 | CTCCCCAGCACAGCC[A/C]TGGACCACTCAGCTG | 899 |
rs778575701 | snp | A/G | 1.70673e-05 | 0.00292119 | intron-variant | CCNF | GRCh38.p7 | 16:2430964 | GCCACTCCTTTACAT[A/G]ATCTTTGTTTGGGAC | 899 |
rs778591493 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2438852 | AAAACACAAAAATTA[C/G]CCGGGCATGGTGGTG | 899 |
rs778657072 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433088 | TCTGCACCCTGAGAA[C/T]GGCTCAGTCTTCTCC | 899 |
rs778667431 | snp | C/G | 6.61135e-05 | 0.00574912 | missense | CCNF | GRCh38.p7 | 16:2453304 | GGAGAAATCAGCCAG[C/G]AAGAGGTGCCTCCCT | 899 |
rs778688654 | snp | A/G | 0.000193622 | 0.00983736 | intron-variant | CCNF | GRCh38.p7 | 16:2449166 | GCGCTGGTGCGCTAC[A/G]CGTGCAGCATCGGCG | 899 |
rs778712309 | snp | C/G | 1.6554e-05 | 0.00287693 | | | GRCh38.p7 | 16:2438035 | CGGGCAGTTCTCTGT[C/G]CTGGAAATCACACTT | 899 |
rs778768659 | snp | C/T | 6.61583e-05 | 0.00575107 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453460 | AGTGACACAAGACAG[C/T]CCCGACCCCCCGACT | 899 |
rs778842501 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2437848 | AGCTTGCAATGAGCC[A/G]TGACTATGCCAATGC | 899 |
rs778844511 | snp | G/T | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457657 | CCAGAGGCGTTCGTA[G/T]GTGACCCACAGATGG | 899 |
rs778846449 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2446531 | GGAAATAACGTGGAA[A/G]TGATTCTCACAATAC | 899 |
rs778936163 | snp | A/G | | | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447725 | CACTGCACTAATCCA[A/G]CCTGGGTGACAGAGG | 899 |
rs778941605 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441901 | CATAAGAGTGCACTT[G/T]TAAATGAGATATTTT | 899 |
rs778959034 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454835 | GAGGCCGAGGTGGGC[A/G]GATCACCTGAAGTTA | 899 |
rs778996095 | snp | C/T | 3.31581e-05 | 0.00407161 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445503 | TGCCACCATGAAGGA[C/T]TTCACAAGCCTGTGC | 899 |
rs778998058 | snp | C/T | 1.72445e-05 | 0.00293632 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449438 | GCCGCAGCCCTGCTC[C/T]TGGCCAGACTGACGC | 899 |
rs779047539 | in-del | -/T | 0.000144519 | 0.00849933 | intron-variant | CCNF | GRCh38.p7 | 16:2439716 | CCTCCCAAGACACAG[-/T]TGTACAAAGGCTCGG | 899 |
rs779053179 | snp | A/C/G | 0.00660265 | 0.0570803 | missense | CCNF | GRCh38.p7 | 16:2449387 | CTCTCCCTGCTGCAC[A/C/G]CCAGCCTGTCCGCCT | 899 |
rs779143179 | snp | C/T | 1.89349e-05 | 0.00307686 | missense | CCNF | GRCh38.p7 | 16:2455411 | AAGCGGGAGAACAGC[C/T]TCCAGGAAGACAGAG | 899 |
rs779318402 | snp | A/G | 1.77637e-05 | 0.00298019 | intron-variant | CCNF | GRCh38.p7 | 16:2439861 | TGACGTGGGGAGCTG[A/G]CCTTTCTCCCTCCAG | 899 |
rs779326906 | snp | C/T | 2.2565e-05 | 0.00335886 | intron-variant | CCNF | GRCh38.p7 | 16:2432950 | CAGCCCCGGCCCCCG[C/T]TGTTCTGCAGGTACA | 899 |
rs779348473 | snp | C/T | 3.29696e-05 | 0.00406001 | missense | CCNF | GRCh38.p7 | 16:2448883 | GAGATCCTGACCATC[C/T]GGGAGGCCGTATGGC | 899 |
rs779403661 | snp | A/G | 3.29544e-05 | 0.00405908 | intron-variant | CCNF | GRCh38.p7 | 16:2449918 | TCCATAAGAAGTGGT[A/G]AGTTTTGGCCGGGCG | 899 |
rs779410813 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2450857 | CAGGAAAATACTCCC[C/G]TTCCCTTGAGAGAAC | 899 |
rs779434402 | snp | C/G | 2.15065e-05 | 0.00327915 | synonymous-codon, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457017 | GGGCCTTGTGAGGCT[C/G]TAAGTGTGTCAGCAC | 899 |
rs779441312 | snp | A/G | 3.3065e-05 | 0.00406588 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437199 | CTTCAGTCTCGCTGA[A/G]CGGCTGAATGTGGGT | 899 |
rs779513022 | snp | C/G | 7.30674e-05 | 0.00604387 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456582 | CGATGTCACCGTGGT[C/G]TACCTGAACCCAGAA | 899 |
rs779564332 | snp | A/G | 0.000186168 | 0.0096462 | intron-variant | CCNF | GRCh38.p7 | 16:2449178 | TACGCGTGCAGCATC[A/G]GCGTGAACATCATCC | 899 |
rs779567997 | snp | A/G | 5.51151e-05 | 0.00524924 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445388 | CGGGCCCAACAGGTG[A/G]GGTTGAAATCGCAGA | 899 |
rs779594258 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2430233 | CGCTTCCTTTCAGGA[C/G]TGGAAGGAAGGATGG | 899 |
rs779690461 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2431941 | GTTCATGCCATTCTC[C/T]TACCTCAGCCTTCCG | 899 |
rs779696796 | snp | C/T | 0.000118569 | 0.00769872 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437151 | GTCTGATGAGGCCCG[C/T]GCAGAAGTGAATGGC | 899 |
rs779744110 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2437772 | GGGGTGGTGGTGCAT[A/T]CCTATAGTCCCAGCT | 899 |
rs779751767 | snp | C/T | 1.72148e-05 | 0.00293379 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437135 | TCCCCGCAGTGTCTG[C/T]GTCTGATGAGGCCCG | 899 |
rs779898364 | snp | C/T | 1.66927e-05 | 0.00288895 | intron-variant | CCNF | GRCh38.p7 | 16:2449269 | GAGCCCACACCCCGT[C/T]CCGGCTGTCTAGGTC | 899 |
rs779915331 | snp | C/T | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2431206 | GCCCCGAAACCTGAC[C/T]ATCTTGAGTCTCCCC | 899 |
rs779926230 | snp | C/T | 1.65162e-05 | 0.00287365 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456887 | CCTGCCACCATCAGG[C/T]CAGGAAGTCATGTTT | 899 |
rs779972411 | snp | C/T | 3.33328e-05 | 0.00408231 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456756 | GAAGGACGTCACGAC[C/T]TCAGGGTACTCCTCC | 899 |
rs780045668 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2453035 | TTCCTGGGTCTTTAC[C/G]TAGAGAGGAATTGCT | 899 |
rs780069269 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454073 | GATGAACAGGGCCCT[C/T]CCTGTGCTGCTGGCC | 899 |
rs780130243 | snp | A/G | 1.79377e-05 | 0.00299475 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445650 | CTTGGCCCAGCTGGC[A/G]GGGACGTGCTGGCCT | 899 |
rs780155682 | snp | C/T | 3.31477e-05 | 0.00407096 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456804 | CACAAGCTCCGTGGA[C/T]GGTGGCTTGGGGGCC | 899 |
rs780182455 | in-del | -/TGT | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445725 | TTTGGTTTTGTTTTG[-/TGT]TGTTTTTTTTTTTTT | 899 |
rs780195674 | snp | C/T | 6.95156e-05 | 0.00589517 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449447 | CTGCTCCTGGCCAGA[C/T]TGACGCACGGGCAGA | 899 |
rs780210521 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2434029 | AGTGTATAACTCAGC[C/T]GGGTGTGGCGTCACA | 899 |
rs780211194 | snp | C/G | 8.28411e-05 | 0.00643535 | intron-variant | CCNF | GRCh38.p7 | 16:2453389 | GGGCCTCTGCACCCC[C/G]TAACTCTAGCTTCCC | 899 |
rs780251759 | snp | A/G | 9.39382e-05 | 0.00685276 | intron-variant | CCNF | GRCh38.p7 | 16:2449497 | AGGGATGCCTGTGTC[A/G]GGGAAGGTGCTGACA | 899 |
rs780471402 | in-del | -/CT | 1.65696e-05 | 0.00287828 | intron-variant | CCNF | GRCh38.p7 | 16:2453198 | GTCCACTCCACGTGA[-/CT]CTGTTTCCAGCTTCC | 899 |
rs780532687 | snp | C/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428111 | TGGGACATCTGGGGA[C/G]CAGGCCCCAAACTCG | 899 |
rs780572208 | snp | C/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427996 | CCTGAAAGTGCACCT[C/G]TGCCCTAGGGGGAGA | 899 |
rs780573440 | snp | A/T | 1.67206e-05 | 0.00289137 | intron-variant | CCNF | GRCh38.p7 | 16:2435756 | GCTGTAGTAGTTCAT[A/T]ACGTTTGTGGCATAA | 899 |
rs780598425 | snp | C/G/T | 4.95318e-05 | 0.00497633 | intron-variant | CCNF | GRCh38.p7 | 16:2448988 | ATTCGAGTAAGCAGC[C/G/T]GTTCCATTTTCCTTA | 899 |
rs780647051 | in-del | -/TT | 4.98965e-05 | 0.00499457 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443603 | GAAATGGAAAACTGC[-/TT]AACATGGCTGCTGTC | 899 |
rs780649554 | snp | A/C | 1.67156e-05 | 0.00289093 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456698 | CCCAGATCCCTGCAA[A/C]CCCTGGACCCAAACC | 899 |
rs780656173 | snp | A/G | 3.81359e-05 | 0.00436652 | intron-variant | CCNF | GRCh38.p7 | 16:2449066 | TTTCCTGCTGTGGGA[A/G]GGCCTCATGGACTCA | 899 |
rs780679252 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458706 | GGGTGTGGTCGGGGT[A/G]AGAACCCAAGCGTTG | 899 |
rs780730595 | snp | C/T | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457980 | AGAGCAGTCGGGGGC[C/T]GTGTCCTGGCTGATC | 899 |
rs780761155 | snp | C/T | 8.29071e-05 | 0.00643791 | intron-variant | CCNF | GRCh38.p7 | 16:2453193 | CACATGTCCACTCCA[C/T]GTGACTCTGTTTCCA | 899 |
rs780829450 | snp | C/G | 0.000123785 | 0.00786622 | intron-variant | CCNF | GRCh38.p7 | 16:2437108 | AGACATCCCTGGGCT[C/G]TGTCCTGTCTGTCCC | 899 |
rs780925478 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454963 | TACTCAGGAGCCTGA[C/G]GCAGGAGACTCACTT | 899 |
rs780961366 | in-del | -/GAATAAGGGAACAATGAACTCTGCTGG | 6.99717e-05 | 0.00591447 | intron-variant | CCNF | GRCh38.p7 | 16:2439314 | AATAAAAATGAAAAA[-/GAATAAGGGAACAATGAACTCTGCTGG]GATTTATTCTAGGAT | 899 |
rs780974312 | snp | A/G | 3.59758e-05 | 0.00424106 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437281 | AGCTGCTGCAAGGCC[A/G]TGGTTCACGAGAGCC | 899 |
rs781029092 | snp | A/G | 1.6537e-05 | 0.00287545 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437207 | TCGCTGAGCGGCTGA[A/G]TGTGGGTGCCGCACC | 899 |
rs781029145 | snp | A/G | 0.000514024 | 0.0160233 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445484 | TCGACTGGCTGGTGG[A/G]AGTTGCCACCATGAA | 899 |
rs781073147 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2436177 | GCTCCCTGCCCTGTG[C/T]GCCATGAGCACGCAG | 899 |
rs781152137 | snp | A/C | 1.79728e-05 | 0.00299768 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445401 | TGGGGTTGAAATCGC[A/C]GACAGGGACACATGG | 899 |
rs781175835 | in-del | -/CAGG | | | intron-variant | CCNF | GRCh38.p7 | 16:2455296 | GGGAGCACGTGGTGA[-/CAGG]CTGGGGCACGCGGGT | 899 |
rs781183007 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2432539 | AGACCTCCATCATGG[A/G]TGTTGTTCTTTGCCC | 899 |
rs781217308 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2432735 | TTCCTCCTTCCCAGA[C/T]CATTGTCCTCTGCCC | 899 |
rs781247687 | snp | A/C/G/T | 5.05382e-05 | 0.00502665 | intron-variant | CCNF | GRCh38.p7 | 16:2449239 | GCACTGCACCAAGGA[A/C/G/T]CCCCCGAGCGCTGAG | 899 |
rs781263300 | snp | C/G | 2.6782e-05 | 0.00365927 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439375 | AGAAGCAGCAGCAGG[C/G]CCATGACCTGTTTGA | 899 |
rs781411948 | snp | C/T | 8.24436e-05 | 0.00641989 | intron-variant | CCNF | GRCh38.p7 | 16:2448849 | GACCCCTTCTCGGCG[C/T]TGCAGGTTTATCAGT | 899 |
rs781500182 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2439972 | ACACCCTAAGATCGG[A/T]TCAGCACTGGAACTG | 899 |
rs781622825 | snp | G/T | 1.64751e-05 | 0.00287007 | missense | CCNF | GRCh38.p7 | 16:2449891 | AAGACCTCATTCCCT[G/T]CGTCTTGAGCCTCCA | 899 |
rs781701989 | snp | A/G | 3.29484e-05 | 0.00405871 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443718 | GCTTCCAGTGAGATC[A/G]TCTGCCAGCTATTTC | 899 |
rs781709990 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2453135 | TTTGCATTCTCATTG[C/G]TCACTTCAGTGAACT | 899 |
rs781712247 | snp | C/G | 0.000115667 | 0.00760396 | intron-variant | CCNF | GRCh38.p7 | 16:2435888 | CGTAAGTCCTCACCC[C/G]ACCTGCATGTTGGCG | 899 |
rs781712849 | snp | C/T | 1.76791e-05 | 0.00297308 | intron-variant | CCNF | GRCh38.p7 | 16:2449804 | CCTCCATCCCCTCCA[C/T]CCCTGGCCTGCTTTC | 899 |
rs781741393 | snp | C/T | 5.16996e-05 | 0.00508401 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455533 | TGGCTATGAAGGCGA[C/T]CAGGAGAGTGAGGGC | 899 |
rs781744926 | in-del | -/CT | 1.6563e-05 | 0.00287771 | intron-variant | CCNF | GRCh38.p7 | 16:2453393 | CTCTGCACCCCCTAA[-/CT]CTAGCTTCCCCTCAG | 899 |
rs781774219 | in-del | -/TCCCCTCCC/TCCCCTCCG | 5.00917e-05 | 0.00500437 | intron-variant | CCNF | GRCh38.p7 | 16:2449794 | CCTCCGTCCCCTCCA[-/TCCCCTCCC/TCCCCTCCG]TCCCCTCCACCCCTG | 899 |
rs781779692 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2440532 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 899 |
rs781781103 | snp | C/G | 1.81893e-05 | 0.00301568 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455446 | CTTCGTTACCACCCC[C/G]ACTGCGGAGCTGTCC | 899 |
rs796077740 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2453683 | ACCCTGGGACGGAGC[A/C]CTGCAGTCATGCCTC | 899 |
rs796130563 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2447843 | CTCACACCCCACGCT[A/G]GGCTCTCATTGGCCA | 899 |
rs796156630 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452786 | TTCCATATAAATGGC[A/G]TCATCGGACAAGTGG | 899 |
rs796189263 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440951 | AAAATTAGCTGGATG[C/G]GCTGGGTGCAAGTGG | 899 |
rs796192463 | in-del | -/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2435267 | AAAAAAAAAAGAAAA[-/G]AAAAGAAAAAAAAAA | 899 |
rs796272963 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2441981 | TATATATATATATAT[A/G]TGTTTTTGTTTTTGT | 899 |
rs796285247 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435668 | ATGCACACACACACA[C/T]ATATATATATATATA | 899 |
rs796300912 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2430427 | TCTGAGAAGCATGTC[C/T]GGGCTGCCTGCCTGG | 899 |
rs796420254 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435680 | ACATATATATATATA[C/T]ATATATATATATATA | 899 |
rs796441030 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2450525 | AAAAAAAAAAAAAAA[-/A]GTTCCAGTAGTTTCT | 899 |
rs796446094 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2435273 | AAAAGAAAAGAAAAG[-/A]AAAAAAAAAAGAAAT | 899 |
rs796460904 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440434 | GACCAGCCTGGCCAA[C/G]ATGGTGAAACCATCG | 899 |
rs796493001 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442682 | TATTATATATAATAT[C/T]ATATTATTATATAAT | 899 |
rs796533241 | in-del | -/AT | | | intron-variant | CCNF | GRCh38.p7 | 16:2442734 | TATATATTGTATAAC[-/AT]ATAATTATATAATAA | 899 |
rs796534254 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454181 | TCAATATAGGACCAG[G/T]CAGGGCTGCCTCCAG | 899 |
rs796548309 | in-del | -/TATAA | | | intron-variant | CCNF | GRCh38.p7 | 16:2442751 | TAATTATATAATAAT[-/TATAA]TATAATAATATAATA | 899 |
rs796573028 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2429753 | GCCCTTTCCTGGGGC[A/G]ACGATCGGGTCCCGG | 899 |
rs796595384 | snp | A/C | | | intron-variant, missense | CCNF | GRCh38.p7 | 16:2433064 | ACCTGAAGCTCTTTG[A/C]AAGGTATCTCTGCAC | 899 |
rs796616433 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435684 | ATATATATATATATA[C/T]ATATATATATATATA | 899 |
rs796625816 | in-del | -/TAT | | | intron-variant | CCNF | GRCh38.p7 | 16:2442684 | TTATATATAATATCA[-/TAT]TATTATATAATAATT | 899 |
rs796636178 | in-del | -/ATATA | | | intron-variant | CCNF | GRCh38.p7 | 16:2442937 | ATATATATGATTATT[-/ATATA]ATATATTATTATATT | 899 |
rs796648135 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2429805 | TCCCGGGGCGGCGAT[C/T]GGGTCTCGGGGAGCC | 899 |
rs796667374 | in-del | -/AT | | | intron-variant | CCNF | GRCh38.p7 | 16:2435611 | GATATATATATATAT[-/AT]GCACACACACACACA | 899 |
rs796705348 | in-del | -/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2437866 | CTATGCCAATGCACT[-/C]CCAGCCTGGGTGACA | 899 |
rs796790219 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2450372 | AAAAATTAGCTGGGC[C/G]TGGTGGCATGCGCCT | 899 |
rs796845257 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2429649 | GATGTCGCGTCCCGC[G/T]CAGGGAGCCCCGGCG | 899 |
rs796848982 | snp | G/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445146 | GCCCCGAGGGTCAGG[G/T]TTCATCCACTGTGGG | 899 |
rs796864081 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454309 | AAGCGTGACAGCACT[C/T]TCCATTGTGTGGAAG | 899 |
rs796879949 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2442698 | ATATTATTATATAAT[-/A]ATTATATATAAATAT | 899 |
rs796942350 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427928 | TGGTGTGGCTAATGT[A/G]CTCATGGCTGGCTCT | 899 |
rs797015802 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434104 | TGAGGTCGGGAGTTC[A/G]AGACCAGCCCGGCCA | 899 |