SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs530059837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324048 | GAAAGCAGTTCTGAG[C/T]CCCATAACTTATTTA | 51433 |
rs530069223 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350961 | TAGTAATATTGAGCA[-/T]TTACTACATGCTAGT | 51433 |
rs530074468 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317506 | ATCTGCCCACCTCAG[C/T]CTCCCAAAGTGCTGG | 51433 |
rs530076398 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309173 | AAAAAAAAAAAGGCC[A/G]GGCGCAGTGGCTCAC | 51433 |
rs530140760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316993 | AGCCAATCAAAAAAG[C/G]CCACATTTATATGAG | 51433 |
rs530237711 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338362 | TGGGAGGCCGAGGAG[A/G]GCAGATCATGAGGTC | 51433 |
rs530248932 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323260 | TTGAAATGTTTTCAT[A/G]TTTTTGGGCCATGCT | 51433 |
rs530299795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344647 | CTCGTGGTCAGGGAG[A/G]CCCGTCTGAGGAAAG | 51433 |
rs530405928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344214 | AAGAGGCAGGGGAAA[A/C]AGATAAGCAAGCAAG | 51433 |
rs530420726 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317411 | GGCACGTGCCACCAC[G/T]CCCGGCTAATTTTTG | 51433 |
rs530478990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350486 | GGAGATCGAGACCAT[C/T]CCGGCTAACACGGTG | 51433 |
rs530502305 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325822 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 51433 |
rs530563166 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314435 | CAAACAAAAACCCAT[A/G]TGATCAAATCAATCA | 51433 |
rs530573503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351094 | TAACACATGACGGCC[A/G]GGCGCAGTGGCTCAC | 51433 |
rs530638040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321730 | TTTAGTAGAGGCAGT[A/G]TTTTGCCATGTTGGC | 51433 |
rs530745579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321036 | GGGTGGATCACCTGA[A/G]GTTGGGAGTTCGAGA | 51433 |
rs530751926 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354454 | CCTCATGCCTGGTTT[C/T]TGTTTTCTCAATCGC | 51433 |
rs530822279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336124 | TTATTAATGTACAAG[C/T]TAAAACACACTGAGA | 51433 |
rs530866677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329763 | TGGGATCACAGGCAT[A/G]TCCCACCACACCCAG | 51433 |
rs530932669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336856 | CGAGTTGTTTGCCTA[C/T]CAAGAACACGATTTC | 51433 |
rs530999642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342475 | GTGAGGCCAAAAACC[A/G]TAAAACTCTTAGAAG | 51433 |
rs531198602 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327732 | GAGGGGTGAGGTAGC[A/G]ACAGAACTCCAGGAT | 51433 |
rs531357714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327888 | GTTTTGGGGTTCAGG[C/T]GACACTCAACTAGAG | 51433 |
rs531401599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334582 | TTTGAAAGTTGTTTT[A/G]TCTACTTAATTCTAT | 51433 |
rs531412557 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341044 | CATCCATAAGAAATG[C/T]TTGGGCTGGGCGTGG | 51433 |
rs531461251 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323156 | ACCAGAACTCTGTGC[A/T]TTTCTTCCTCTAACA | 51433 |
rs531478162 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320587 | GAGAGATACTGGTCA[A/G]AGACTCAAATTTCTT | 51433 |
rs531541530 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333896 | CATCCCTCCCACATT[A/T]CTTATATGATATGGC | 51433 |
rs531625920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311552 | ATTCAACAATAATAG[G/T]CCAGGCACAGTATCT | 51433 |
rs531759613 | in-del | -/AAAC | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336682 | GAAACTCAGTCTCCA[-/AAAC]AAACAAACAAACAAA | 51433 |
rs531877331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332941 | TCACTTGAGACCAGG[C/T]GTTCAAGAACAACCT | 51433 |
rs531914298 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324502 | GATGGAATTATTAAT[A/G]TAGACCCAAAGAGCA | 51433 |
rs531989085 | snp | C/T | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354436 | ATGGGCCACTGCATG[C/T]AGCCTCATGCCTGGT | 51433 |
rs532130205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332468 | GGAAAACAAGAGCAC[C/T]TCACCTTCACTTTCT | 51433 |
rs532232551 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348823 | TGGATAACCCAGCAA[C/T]TGCACTTCTAGGGAA | 51433 |
rs532394717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316402 | TAAACACAAAATTAT[A/C]ATGACTCAGCAATTC | 51433 |
rs532398261 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344912 | TTCCAAAGGGTTTAG[A/G]CAGAAAAGTGCTGGG | 51433 |
rs532466859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316803 | GAAATGTAAAGAGCC[A/G]CTATTCATAACAGCC | 51433 |
rs532617875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350862 | GAAGGCCATCACTCA[C/G]GTAACCATGAATATA | 51433 |
rs532636992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337000 | CGACGCGGGCAGATC[A/G]TGAGGTCAGGAGATC | 51433 |
rs532655400 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351564 | CCAGGTTCTAGCGAT[G/T]CTCCTGCCTCAGCCT | 51433 |
rs532679710 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350447 | AGCACTTTGGGAGGC[C/T]GAGGCGGACAGATCA | 51433 |
rs532780935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344177 | AAACAAGACAGAGAA[A/G]GGTCTCAGTTCTCAA | 51433 |
rs532912903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314663 | CTTGCTGTTGCCCAA[C/T]CTGTAGTGCAGTGGC | 51433 |
rs532953384 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320985 | CCAGGCATGGTGGCT[A/C]ACGCCTGTAATCCCA | 51433 |
rs532957597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315367 | GCAATGTTCTCCAAA[A/C]TGACCTACAGATTCA | 51433 |
rs532967136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328953 | CCTATCATGAGCAAC[A/G]AAATTATCTTGTCAT | 51433 |
rs533136122 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335476 | AGGCCAAACAGCAGA[A/C]TTTTTATTGTCATCG | 51433 |
rs533209176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341848 | GAGCTACAAGTGCTT[C/T]GTTAGTGAGGCAGAG | 51433 |
rs533336307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342371 | ATGCAAAAGCATGAA[A/G]GTGGATCCTTATCTA | 51433 |
rs533376106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312885 | GCTCTGTCTCAAAAA[A/C]AAAATACACAGACTC | 51433 |
rs533432140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334196 | AGATGGACTGCTTGC[C/T]TGAGCCCATGAGTTT | 51433 |
rs533521601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313385 | TAAAGCTAACTAACA[A/G]AACCAAGGAAAAAAT | 51433 |
rs533545739 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311041 | AAACTTTTTTTTTTT[A/T]AAGTATCCACTGTAT | 51433 |
rs533787809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310428 | ATTAGCTGAGCATGG[C/T]TGCACATGCCTGCAG | 51433 |
rs534015586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352320 | GGGATTGAAGTAGAG[A/G]CTCTCGTGGACGCTG | 51433 |
rs534022812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332727 | ATAGATCCAAGACCA[A/G]AAACAAAGAAGCCTG | 51433 |
rs534033853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332066 | TGGTAAACTTCTGGC[C/T]TCAGGCGATCCTCCT | 51433 |
rs534121650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317168 | AATTAGATAGCAGTA[A/G]TGGTTGCACAATGTT | 51433 |
rs534294635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330780 | GGGACAAAATGAATC[A/C]TCTCAAATACTCTTT | 51433 |
rs534303028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322099 | TCGATCTCATGACCT[C/T]GTGATCCGCCTGCCT | 51433 |
rs534314883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309375 | CCTGGAAGGCGGAGG[C/T]TGCAGTGAGCCGAGA | 51433 |
rs534358988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330144 | CGTATTTCTTCTCTG[C/T]TGTTGATTTTTTTTT | 51433 |
rs534360611 | snp | A/G | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337870 | TTCCAGGCAGGTAAT[A/G]TGTTTGCTTCTTGTA | 51433 |
rs534407206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316560 | AACACAGTGAAACCC[C/T]ATCTCTACTAAAAAT | 51433 |
rs534542102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342815 | AGCGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 51433 |
rs534603473 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350228 | AAAGCCTTTATAAAC[G/T]ATACTAAGGAATATA | 51433 |
rs534685932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314970 | GTATTGGAAGTTTTA[C/G]TCAAAGCATTTAAGC | 51433 |
rs534716342 | snp | C/G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334938 | CGGCAATGTTACATA[C/G/T]TGACACTAGGGGGCA | 51433 |
rs534728875 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343719 | TTCCCCATTTATAAA[C/G]AATGTCACCCCCTGC | 51433 |
rs534844886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350490 | ATCGAGACCATCCCG[A/G]CTAACACGGTGAAAC | 51433 |
rs534883758 | in-del | -/TATATTATAAAGTA | 0.00755907 | 0.0610114 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338739 | ATTAATACTTTAGTG[-/TATATTATAAAGTA]TATATTATCCTAGTC | 51433 |
rs535020552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321153 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATCGCTTG | 51433 |
rs535083141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329136 | TGAATCAATGGACAA[A/G]CTACAGATTTGTTTT | 51433 |
rs535124962 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334484 | CAGGGCAGGTGGGGG[A/G/T]GTGAAGGGATCTTTG | 51433 |
rs535134226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348798 | ACTGCATATATGCCA[A/G]CTTTAGATGTGGATA | 51433 |
rs535290408 | snp | A/C | 1.68883e-05 | 0.00290584 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341977 | ACTAGAACAGAAGTT[A/C]ATGATAAATTACAGA | 51433 |
rs535292809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319243 | CTGTATTTTCTTTTT[C/T]TTTTTTTGGAGATGG | 51433 |
rs535352096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326592 | GACCTGCCTCTGACA[C/T]TTACAGGTGTTGGAT | 51433 |
rs535357371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341418 | GAGGTAGCAGGGACC[C/T]GAGATCATGCCACTG | 51433 |
rs535496345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333181 | ATTAGTTGGGCATGG[C/T]GGCATGCACCTGTAG | 51433 |
rs535538163 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355618 | AATCCCAGCACCTTG[A/G]GAGGCAGAGGTGGGT | 51433 |
rs535592374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346782 | CAAACTGCAACACCT[C/T]CAACATCCCCACTGT | 51433 |
rs535637271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319927 | TTACAATAATTCACA[C/G]ATATTCTTTTTTGGG | 51433 |
rs535700772 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354215 | GCTGGTCTTGAACTG[G/T]TTGAACTCCTGACCT | 51433 |
rs535818940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325997 | GAGGGAAGAAACAAG[C/T]GAGAGACAGACTTGC | 51433 |
rs535855657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317330 | ACGATCCTGGCTCAC[C/T]GCAACCTCCGCCTCC | 51433 |
rs535940295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332535 | ACAACTATGCTTAGC[A/G]TTGTTTATTCCCTAT | 51433 |
rs535971860 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326706 | TGAGACAGTACCCAT[A/T]AAATAGGCACAGGGA | 51433 |
rs536076982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346258 | CCCCACCTCCACCTG[A/C]AGGCTTCCATTTTAC | 51433 |
rs536136780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353214 | CAAAATCTATACTCT[G/T]CATTTCAAAGCCCTC | 51433 |
rs536318580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323520 | TATATTTTGTAGAGA[C/T]GGGGTTTCACCATGT | 51433 |
rs536381520 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307891 | CATGCAGAATATATA[A/G]GAAAGCCAACATCTA | 51433 |
rs536446580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322607 | ATCAATTATGGTACA[A/T]GAAAATAATCTGGTT | 51433 |
rs536480245 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311602 | CTTTGGGAAGCTGAG[A/G]CAGGTGGATCTCTTG | 51433 |
rs536497001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338482 | TAATCCTAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51433 |
rs536504934 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338100 | TTCTAAGGGCAGGGT[A/G]TGGTGGTTGATGCCT | 51433 |
rs536517298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309073 | AGAGTCACTTGAACC[C/T]GGGAGGCAGAGGTTG | 51433 |
rs536517343 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339658 | TGTTTTAATAGAGAC[A/G]GGGTTTCACCATGTT | 51433 |
rs536567714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344408 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 51433 |
rs536632343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337177 | GAGCCAAGGTCGTGC[C/T]ACTGCACTCCAGCCT | 51433 |
rs536681068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351609 | ATTACAGGTGCCCGC[C/T]ACCACGTCCAGCTAA | 51433 |
rs536769571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350160 | ATGGTGTCCTCAGTT[A/C]TCCCCTCTTCCCATG | 51433 |
rs536836503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315841 | GCATTAAAACTATAA[A/T]ACTGTGAGAAGAAAA | 51433 |
rs536868037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314890 | CCTTGGCCTCAAAAA[A/G]TGCTGGGATTACAGG | 51433 |
rs536982353 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314118 | ATGAAAGAAAAAATC[A/G]GGGCTGGGCGCAGTG | 51433 |
rs536986084 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337490 | ATTTTCTTTTCTACA[G/T]GGGTCCCTTCAGGCT | 51433 |
rs537042716 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320666 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCATTGC | 51433 |
rs537091790 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345722 | GTTAACTTCCCAGAT[C/G]TGGAAGGGTAAAAAG | 51433 |
rs537123234 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327488 | CTCCCAGATCCCCCC[C/G]CCCCCACCCCATGTT | 51433 |
rs537291051 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337030 | CAAGACCATCCTGGC[A/C]AACATGGTGAAACCC | 51433 |
rs537330026 | in-del | -/AGTTACTGACT | 0.00478085 | 0.0486577 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335014 | GGTTCCCTCTATGGA[-/AGTTACTGACT]AGTTACTGACTAGTC | 51433 |
rs537527168 | snp | A/G | 0.000132308 | 0.00813243 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335559 | GCGGCAGTGCAGGGC[A/G]GCAAGATTCAGAGCG | 51433 |
rs537686223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341302 | TGGTGAAACCCCATC[C/T]CTACTAAAGATACAA | 51433 |
rs537697312 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340735 | TTTTTGTGTGTGTGT[G/T]TTTTTTAGCAGAAAC | 51433 |
rs537718714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333088 | TGGGAGGCCGAGGCA[A/G]GTGGATCACCTGAGG | 51433 |
rs537755465 | snp | C/T | | | missense | ANAPC5 | GRCh38.p7 | 12:121318501 | CAAGAGACCCCTTAC[C/T]TGATCACCATTTCTG | 51433 |
rs537760405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347996 | ATCACTCCAAACATG[A/C]AAATAAGGATTTTTC | 51433 |
rs537838667 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340054 | AGGCGCAGTGGCTCA[A/C]GCCTGTAATCCCAGC | 51433 |
rs537969607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352856 | TGGGCTCGAGCGATC[C/T]TCCCGCCTTCCCGAG | 51433 |
rs537978691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311238 | GCACTCCAGCCTGGA[C/T]GACTGAGTGAGACCC | 51433 |
rs538032930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326494 | TATAAAGAGAATCTC[A/G]TCAAATTACTTGAGC | 51433 |
rs538045118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325923 | TACCAGATGCTTCTC[C/T]TATCCAAGGCACCAG | 51433 |
rs538179411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317317 | GGAGTACGGTGTCAC[A/G]ATCCTGGCTCACTGC | 51433 |
rs538220689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332844 | TACCCATTGATAATA[C/T]TGTAAACATAGACAA | 51433 |
rs538229221 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338457 | AGCCGGGTGTGGTGG[C/T]GCACACCTGTAATCC | 51433 |
rs538257033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322885 | AAAAAATAAGCCGGG[C/T]GCAGTGGCAGGTGCC | 51433 |
rs538263867 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331840 | CAAAATCACTTTTAT[A/G]TTTGTTTGTTTGTTT | 51433 |
rs538286971 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339551 | TCTTGGCTCACTGCA[A/T]ACTCCGCCTCATGGG | 51433 |
rs538327448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338456 | TAGCCGGGTGTGGTG[A/G]CGCACACCTGTAATC | 51433 |
rs538485218 | in-del | -/AT | 0.00914312 | 0.0669923 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323730 | AGACGCTCAGGCCAC[-/AT]GTGGACTTTTATTTG | 51433 |
rs538519771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343781 | GCAATGCAGTAAATA[A/G]TAAGCTCCCAGGAAA | 51433 |
rs538559450 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349746 | TTTTTTGGAGACGGA[G/T]GCCCAGGCTGGAGTG | 51433 |
rs538895362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351431 | TAGCACACAGTTAAG[C/T]ATTCAATCAGTGCTC | 51433 |
rs538927918 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312163 | CAGTAACAGAAGGAA[A/G]CCAGAAAATTCACAA | 51433 |
rs539016153 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307775 | GTGAGCCACCGCAGC[C/T]GGCCCCCTTAATTTA | 51433 |
rs539028301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315780 | TGGAGCCCTATCTCA[C/T]AGTATATACAAAAAT | 51433 |
rs539101540 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321953 | TCACTGCAACCTCTG[A/C]CTCCCGCGTTCAAGC | 51433 |
rs539110690 | snp | A/C | 6.66989e-05 | 0.00577451 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328292 | TCTAAAGAATTCACA[A/C]CCCCAGGGCCTTGGG | 51433 |
rs539213459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329941 | TTCAATGCCCCTCTG[A/T]GTATGTCATTGAGGA | 51433 |
rs539243963 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329305 | ACTACAGGCGCCCAC[A/C]ACCACGCCCGGCTAA | 51433 |
rs539268313 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319142 | ACACACACACACACA[C/T]GCATGCAGGAAAAAT | 51433 |
rs539288185 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349623 | AATAAAATAACTATA[C/T]AGTAGTTAGCCAGGT | 51433 |
rs539304290 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348021 | TTTTTCTATCTACCT[A/G]AAACACTAAAGTAAT | 51433 |
rs539312935 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334829 | TTTTACCTCCAAAAA[A/T]TCCTTTAGGGACTCT | 51433 |
rs539322324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320069 | CTGCTTCATATACTA[C/T]TAGATACCAATGAAG | 51433 |
rs539448052 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342540 | AATACATTTTTAAAT[-/A]AAAAAAAATTAAAAA | 51433 |
rs539489475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326760 | CAACATTAGTTATTA[C/T]GATTTCAGATATACT | 51433 |
rs539612750 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313986 | ACAGATGCAAAAATT[A/C]TCAACAAAATACTTG | 51433 |
rs539671812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347955 | TTGCAAACATAAATT[A/C]ATTTATCAACCCCTC | 51433 |
rs539802000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319306 | GGTGCGATCTTGGCT[C/T]ACTGCAACCTCCGCC | 51433 |
rs539850575 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355927 | CAATCCTCATCAATC[A/G]TTATTGGGTTTTTTG | 51433 |
rs540019117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308947 | TGAGGTCAGGAGTTC[A/G]ACGCCAGCCTGGCCA | 51433 |
rs540032692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317415 | CGTGCCACCACGCCC[A/G]GCTAATTTTTGTATT | 51433 |
rs540072356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340242 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 51433 |
rs540086494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347061 | TTGAATAATTTCTCA[A/T]GTTTCATATTCCTCA | 51433 |
rs540125956 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355080 | GCAAACTGAAGTTGC[A/C]ATCTAAACTAAATGC | 51433 |
rs540134782 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331609 | CAGAAAACACTGACA[A/G]TGGAAATATAGGACA | 51433 |
rs540259128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345576 | GCCAGCCCCCCAGGA[A/C]CCCCAAGAAAGGGAG | 51433 |
rs540266703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353416 | TTGGCTATCCACATG[A/C]ACACACTGTGCCTTG | 51433 |
rs540270440 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321749 | TGCCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC | 51433 |
rs540299514 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350112 | CAAGTTATAAAGACA[A/T]CCCTTTTATTTAACT | 51433 |
rs540329867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352429 | GTCTACATCTCCGCC[C/T]GCCCTCACAATATCC | 51433 |
rs540337231 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342802 | AGGTGGAGGTTGCAG[C/T]GAGCCAAGATCACGC | 51433 |
rs540442646 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351614 | AGGTGCCCGCCACCA[A/C/T]GTCCAGCTAATTTTT | 51433 |
rs540537285 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316014 | AAGACCAAACACAGA[A/C]CAGGAGAAAATATTT | 51433 |
rs540550162 | snp | A/G | 3.46891e-05 | 0.00416453 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331311 | AGGCCAATTCAACCC[A/G]TGAACAAAACTCCCA | 51433 |
rs540657530 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338230 | ATTTAAAAATAATAA[C/T]TTCTTTAAAAAAAAT | 51433 |
rs540659440 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330449 | ATAATTAAAGTCATA[A/T]GAAACTGCCAAGAAT | 51433 |
rs540680366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329524 | TCTGTCACAAACTTC[A/G]TAAGACAGAATGCTT | 51433 |
rs540722851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344114 | CATTCAGGTACAGAA[C/T]ACATTCTATGAGTCA | 51433 |
rs540723102 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320860 | TGCCCGCCTCAGCCT[C/T]CCAAAGTGCTGGAAT | 51433 |
rs540740267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336666 | GCCTGGGCAACAAGA[G/T]CGAAACTCAGTCTCC | 51433 |
rs540744464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328724 | GAAAGAGCCAGCAGG[A/G]CTTTAGCATTAGATG | 51433 |
rs540968769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341748 | ACAGGGTTTTAGGCT[A/G]TTAGTCACATACCAT | 51433 |
rs540982705 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326276 | ATGTTGAGTGTTATG[A/G]TGCAATCTAACAGTA | 51433 |
rs541000869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315340 | GGGTTGGAAGAGAAT[A/G]GCATTAAGATGGCAA | 51433 |
rs541064149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321320 | CACTTACAAAATACA[C/T]GTAAACAAGAACAAA | 51433 |
rs541203866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312686 | CACTCCAGCCTAGGC[A/G]ACAGAGCGAGACTCT | 51433 |
rs541296249 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329336 | TGTTTGTATTTTTAG[C/T]AGAGACGAGCTTTTA | 51433 |
rs541303092 | snp | A/G | 1.89629e-05 | 0.00307914 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319672 | ATTATTTTATTCTGG[A/G]GTTAGAGTTTTCAAG | 51433 |
rs541311079 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341684 | GCTTTTCAGGCTCTC[C/T]TTATGTTTGCAAATG | 51433 |
rs541313636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327013 | TGTCCAACACGTGTC[C/T]AGTGCTTTCCTCAAG | 51433 |
rs541367404 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336170 | AGTTAATTATTTTCA[-/T]TTTTTTTTTAATCAC | 51433 |
rs541537445 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335625 | ATTACTTTTGCTTTC[A/G]GCTCCGGTAAGAATC | 51433 |
rs541626133 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354351 | TTGCGATGTTGTCCA[A/G]GCTGGTCTCGAACTC | 51433 |
rs541701912 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353507 | GTGCAGTGGCGCGAT[C/T]TCTGCTCACTGCAAG | 51433 |
rs541872564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340851 | AGGCGTGAGCCACCA[C/T]GCCCAGCCTCCATCA | 51433 |
rs541873318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332914 | GCACTTTGGGAGGCC[A/G]AGGTGGGAGGATCAC | 51433 |
rs541898410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348247 | GATTAAATAAGATAA[C/T]ACAAAGTGCTTTGTA | 51433 |
rs541938729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339609 | CCAAGTAGCTGGGAC[A/G]ACAGGCACATGCCAC | 51433 |
rs542048071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311426 | AAGGAGGACATTATA[C/T]ACTCATGAAACAGTC | 51433 |
rs542049303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338742 | TAATACTTTAGTGTA[C/T]ATTATCCTAGTCTTT | 51433 |
rs542084723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353675 | TCAATCTCCTGACCT[C/G]GTGATCCTCCCGCCT | 51433 |
rs542109553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310564 | CAAGACTTTGTCTCA[A/G]AATAAAACTAGAAAA | 51433 |
rs542122867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344659 | GAGGCCCGTCTGAGG[A/G]AAGTTGAGCTGTGAT | 51433 |
rs542214643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309510 | TAAAATAGCCATTCA[C/T]TTGTCCTCAATCTTT | 51433 |
rs542216408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308831 | TGAGAGAGAAAAAAC[A/C]AACCACTAGGGTGAG | 51433 |
rs542221764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318174 | CCAGACGTCAATATG[A/G]ACAAATGAAAACTCA | 51433 |
rs542279223 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316702 | TGCACCACTGCACTC[A/C]AGCCTGGGTGACAGA | 51433 |
rs542433855 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322957 | TTGAACCCAGGAGGC[A/T]GAGGTTGCAGTGAGC | 51433 |
rs542491829 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326921 | AGACCTCAAATTCAA[A/C]CAACTTTGCAGACTC | 51433 |
rs542574149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351908 | CTAATAAATACTGGA[A/G]CCAGACATGAACTTG | 51433 |
rs542719138 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316504 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG | 51433 |
rs542748744 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350646 | TGATCGTGCCACTGC[A/C]CTCTGGCCTGAGCGA | 51433 |
rs542803733 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312335 | CTGTGAGGCTGAGGC[A/G]GGTGGATCACCTGAG | 51433 |
rs542848289 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322185 | TTTTTTTGAGAGGGA[G/T]TCTCACTGTGTCACC | 51433 |
rs542851898 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313050 | TAGAAAAGAGGCCGG[G/T]CGCGGTGGTTCACGC | 51433 |
rs542928601 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340381 | CTAACTAAAGCTGTA[A/C]ATATTTACATTTAAC | 51433 |
rs542959982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337520 | TCTGGCCCCTCATCT[C/T]GCCAGCCTTGGCTGG | 51433 |
rs543072413 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343999 | ATAACAGTAGTTAGG[C/G]AAGGAGAAGTAAAAC | 51433 |
rs543074330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336866 | GCCTACCAAGAACAC[A/G]ATTTCCTTCAAGAAC | 51433 |
rs543137179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343106 | TAGAAAATATATTGG[A/C]TTATACATAAATGAC | 51433 |
rs543168070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335202 | CGGAGTTTCACTCTT[A/G]TTGCCCAGGCTGGAG | 51433 |
rs543255341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315169 | CAACCCAAAAATAAA[C/T]GTTTAAAAAAATTTC | 51433 |
rs543305165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348990 | CCATTTGGGGCCTGG[A/C]GCAGTGGCTCACGCC | 51433 |
rs543315836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348507 | CCGTCTCTACTAAAA[A/G]CACAAAAATTAGCCA | 51433 |
rs543316417 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321260 | GTCTCAAAAAAAAAA[A/T]TTTTTTTTTAATTAC | 51433 |
rs543318616 | snp | C/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314550 | AACCTCTATAAAAAA[C/T]CCACAGCTAGCATGA | 51433 |
rs543465606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335765 | TTAAACGCTGTAAAT[A/G]TCTCTGGTGTAAGAC | 51433 |
rs543597520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318884 | AATTAGCTGGGCGTA[A/G]TGGTGGGCACCTGTA | 51433 |
rs543772258 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314624 | AATAAGGACATACAC[-/T]TTTTTTTTTTTTTGA | 51433 |
rs543983738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326892 | TTAGAATTCCCTTCA[C/T]TGATGCCAAAAAAAG | 51433 |
rs544003379 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341337 | TAGCCAAGTGTGGTG[A/G]TGCACGCCTGTAATC | 51433 |
rs544043572 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334243 | ATGATCATACTACTG[A/C/T]ACTCCAGCCTGGGTG | 51433 |
rs544189402 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354973 | AGCCATTGATTCATT[A/T]ATTCAGTAACACTGT | 51433 |
rs544289874 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354314 | CATGGCTAATTTTTT[C/T]ATTTTTTGTAGACAC | 51433 |
rs544304725 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343830 | ACCTCCTTAGGGCAG[A/G]TGGGGCTTAATTCTC | 51433 |
rs544331617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353502 | CTGGAGTGCAGTGGC[A/G]CGATCTCTGCTCACT | 51433 |
rs544389213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352457 | TCCCAGGAAACAGAC[A/T]TCCGCGTGCTCGCGG | 51433 |
rs544413790 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319960 | GATTTAAAATTTTTT[A/T]AAAATATCTCAAGTA | 51433 |
rs544427964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318155 | GCACAGGAAGACTAC[C/T]TTTCCAGACGTCAAT | 51433 |
rs544487564 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324998 | AGTGAGATTCCATCT[C/T]TACAAAAAGATATTT | 51433 |
rs544500225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351823 | TGTATGACTTATCCC[C/T]GTGTCTCCAACGCTC | 51433 |
rs544667167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323216 | AAAGTAGTACCTTAA[C/T]TGCTTTAAATTTAAT | 51433 |
rs544672413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316658 | GAATGGCATGAACCC[A/G]GGAGGCGGAGCTTGC | 51433 |
rs544673718 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322115 | GTGATCCGCCTGCCT[C/T]GGTCTCCCAAAGTGC | 51433 |
rs544747623 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315429 | TTTTTGCAGAAATGA[A/C]CAAGCTAATTCTAAA | 51433 |
rs544787352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330282 | AATAAGCCTTTGCTA[A/C]AATTTTTCTAAGTGA | 51433 |
rs544829395 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349083 | CAGCCTGGACAACAT[C/G]GTGAAATCCCATGCC | 51433 |
rs544943469 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319383 | GATTACAGGCACCCA[C/T]CACCATGCCTGGCTA | 51433 |
rs544950980 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340656 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 51433 |
rs545104692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342395 | TTATCTAACACCATA[G/T]TCAAAAATTAACTCA | 51433 |
rs545280262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313411 | AAAATAAGGATTAAA[A/G]TGGAGATAAACAAAA | 51433 |
rs545555640 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350360 | CAGACAATGCTTATC[C/T]ATCAAGGCACAGCTT | 51433 |
rs545577397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314273 | GCATGGTGGTGCACA[C/T]CTGTGATCCCAGCTA | 51433 |
rs545625631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320763 | GCCTGCCACCATGTC[C/T]GGCTAATTTTTTTGT | 51433 |
rs545686870 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348923 | ATTTATAATACAGAG[C/T]TGAATTATGTTGCTT | 51433 |
rs545708117 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313752 | GACTGAATTAGTAAC[C/T]AAAAAAACTTCCAAC | 51433 |
rs545908153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333487 | AAAAAAAGAAAGGCT[C/G]TGATCGAGAGGTTAT | 51433 |
rs545919351 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318816 | ACAAGGTTAGGAGCT[C/T]GAGACCAGCCTGGCC | 51433 |
rs545969978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325313 | ACAAAAAACATAAAA[A/G]TTAGCTGGGAGTAGT | 51433 |
rs546034893 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332922 | GGAGGCCAAGGTGGG[A/T]GGATCACTTGAGACC | 51433 |
rs546077556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347513 | GTGTATGCTTGTAGT[C/T]CCAGCTACTTGGGAG | 51433 |
rs546377086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344904 | TCTCTAAGTTCCAAA[A/G]GGTTTAGGCAGAAAA | 51433 |
rs546471144 | in-del | -/T | 0.0283406 | 0.115616 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321872 | TGCTGTTGTTGTTGC[-/T]TTTTTTTTTTCTGAG | 51433 |
rs546500007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338866 | TTGTAAACATATATT[A/G]TGTATACATTACATT | 51433 |
rs546532494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316335 | TTGGAACCCTCATAC[A/G]TTGCAGGTTGAAACA | 51433 |
rs546567318 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341420 | GGTAGCAGGGACCCG[A/G]GATCATGCCACTGCA | 51433 |
rs546595545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322413 | ATCTGCCCACCTCAG[C/T]CCCCCAAATTGCTGG | 51433 |
rs546686150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344317 | AGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 51433 |
rs546770509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315465 | CATATAATTGCAAGG[A/G]ATGCTGAATAGCCAA | 51433 |
rs546905232 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343187 | AAGTTAAGAGAAAAC[A/C]AACCCAAATAAGAAA | 51433 |
rs547017784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321893 | TTTTTCTGAGACAGA[A/G]TCTCACTCTGTCACC | 51433 |
rs547074940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329867 | TGATCCACCCACCCC[A/G]GCCTCCCAAAGTGCT | 51433 |
rs547138397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336966 | GGCTCACGCCTGTAA[C/T]CCCAACACTTTGGGA | 51433 |
rs547177366 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327285 | AGACCTGGCTGCGCT[G/T]TGGCCATGCCCGTCA | 51433 |
rs547281082 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335250 | GGCTCACTGCAACCT[C/G]CACCTCCCGGGTTCA | 51433 |
rs547293273 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334682 | TATAAACCAGTGTCA[A/C/T]CTGACTGAGCAGCCT | 51433 |
rs547307338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319950 | TTTTTGGGGGGATTT[A/G]AAATTTTTTTAAAAT | 51433 |
rs547367671 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327318 | TATCTTGAGTGGAGG[C/T]GTAAAGTCATACACC | 51433 |
rs547483004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340646 | CAACCTCCACCTCCC[A/G]GGTTCAAGCGATTCT | 51433 |
rs547487557 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320600 | CAGAGACTCAAATTT[A/C]TTTTCTTTCTTTTTT | 51433 |
rs547585149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347698 | GGGAAAACAACCTAG[A/G]GTAATAAAGGTATCT | 51433 |
rs547598603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328020 | TCACTTGTTAACTGC[A/G]TTTGCGATCGCGGGT | 51433 |
rs547625103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311865 | ACAAAAACCACAATA[A/G]TAGTTGGGGAGCTCA | 51433 |
rs547635537 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334018 | CAGTGGCTCATGCTT[A/G]TAATCCCAGCACTTT | 51433 |
rs547639243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310962 | AAAAAAATCAAATTA[C/G]AAATAATGACATTAA | 51433 |
rs547649093 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355034 | TCTAGGTGCTGGGGA[A/C/T]CAAAAGGGATGAATT | 51433 |
rs548087710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326152 | ACCCCTCAGTTTACA[A/C]AGCCATGTAAGAGAC | 51433 |
rs548224515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352553 | CAAGAGTGCGGGGAG[A/G]GGTGCACCAAAAGAC | 51433 |
rs548298027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333016 | AGAAGAAATTCTGTT[C/T]ATCAAAATATTATTT | 51433 |
rs548369067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339094 | GAGTCTTGCTCTGTC[A/G]CCAAGGCTGGAGTGC | 51433 |
rs548406812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323272 | CATGTTTTTGGGCCA[C/T]GCTTTCTGTGAATGT | 51433 |
rs548474007 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337792 | TCTGCACTTACCCCC[C/G/T]CTGTGGCACTATCAA | 51433 |
rs548515492 | snp | C/T | 1.65359e-05 | 0.00287536 | intron-variant, synonymous-codon, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352239 | CACCAGCACCGCGAT[C/T]TTGTACGGCGTCACC | 51433 |
rs548642455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317519 | AGCCTCCCAAAGTGC[C/T]GGGATTATAGGCATG | 51433 |
rs548644563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343706 | AGTGCGATAAGCATT[A/C]CCCATTTATAAACAA | 51433 |
rs548654088 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339716 | TCAAATGATCCACCC[C/G]CCTTGGCCTTCCAGA | 51433 |
rs548658938 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334616 | CTAAAACATAATTGA[G/T]CGATTTTCCTATTTC | 51433 |
rs548802892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315533 | ATTTCAAAACTTACT[A/G]CAAAGCTATAGTAAT | 51433 |
rs548817075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314956 | CATTTATTCAACATG[C/T]ATTGGAAGTTTTACT | 51433 |
rs548852881 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354527 | ACAAAAACAAAAAAG[A/G]AGGCAGATATGTATA | 51433 |
rs548956815 | in-del | -/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308284 | AAGAAAAAGTTGGTG[-/T]CCTTTGCTACCAAAA | 51433 |
rs549022783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329814 | GAGAGAGGGTTTCAC[A/C]ATGTTGGCCAGGCTA | 51433 |
rs549113976 | in-del | -/TGT | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321861 | ACTTTTGGGTTTTGC[-/TGT]TGTTGTTGCTTTTTT | 51433 |
rs549320437 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331610 | AGAAAACACTGACAG[C/T]GGAAATATAGGACAT | 51433 |
rs549384809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329081 | GAGCCACTTTTGTCA[C/T]TATAATCAATTCTGT | 51433 |
rs549492340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336167 | CTAAGTTAATTATTT[C/T]CATTTTTTTTTTAAT | 51433 |
rs549669234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340608 | GTAGCGCAATCTTGG[C/T]TCACTGCAACCTCCG | 51433 |
rs549730681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347572 | GGAAGTCCAGGCTGC[A/G]TTGAGCCCTGATTGC | 51433 |
rs549732581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340133 | ACCAGCCTGCCCAAC[A/G]TGGCAAAATCCCGTC | 51433 |
rs549737744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326545 | TCCCATTCCCACTGC[C/T]CTTCTTTGGAGTCAA | 51433 |
rs549853282 | snp | C/T | 3.38547e-05 | 0.00411415 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319866 | AATGGCGAATGTTCA[C/T]CTTAATGAGTATATG | 51433 |
rs549893694 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327868 | CAACTTTCTTTTACA[C/T]AATAGTTTTGGGGTT | 51433 |
rs549975466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334620 | AACATAATTGATCGA[C/T]TTTCCTATTTCTATT | 51433 |
rs550010840 | snp | A/G | 0.000399281 | 0.0141238 | missense | ANAPC5 | GRCh38.p7 | 12:121318380 | GGCAGCGCGATGGTA[A/G]GGGAGGAAGATCGCC | 51433 |
rs550221952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311729 | TCCCAGATGCTCAGA[A/G]AAGTGAGGTGGGAGG | 51433 |
rs550336853 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326048 | CCAGCTAGCCCTTTC[A/G]ACCTCAGAAAACATG | 51433 |
rs550394223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339000 | AACTTTATTTCCTGT[C/T]CTTTTCATTTTATAT | 51433 |
rs550511622 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353987 | CCATGCATGGCTAAT[-/T]TTTTTTTTTTTTTTT | 51433 |
rs550653076 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346189 | CCTCCTGGAATGTTC[C/T]TCCCCAGTCCTTTAC | 51433 |
rs550674893 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314589 | GATGAAAGACTGAAC[A/G]CTTTCCCCCTACAGG | 51433 |
rs550762371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344971 | CAGATGCTGCCTGAA[G/T]AACAGATGTAGGGAG | 51433 |
rs550818210 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330499 | CATTCTAAATCTATC[A/G]CTGGTTAATGACAGA | 51433 |
rs550869910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343569 | CACTATGTTGTCTTT[C/T]CACCAGACAAGAAGC | 51433 |
rs550874290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121352162 | AGGAGCAGCTGGTTG[A/C]GCCTCCGCCGCTCCA | 51433 |
rs550931187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350452 | TTTGGGAGGCCGAGG[C/T]GGACAGATCACGAGG | 51433 |
rs550978621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316827 | AACAGCCAAAAGGTG[C/G]AAACGACTCAAATGC | 51433 |
rs551117570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321961 | ACCTCTGCCTCCCGC[A/G]TTCAAGCGATTCTCC | 51433 |
rs551186122 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339185 | ATCCCAAGTAGCTGG[A/G]ATTACAAGCATCCAC | 51433 |
rs551192428 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329949 | CCCTCTGTGTATGTC[A/T]TTGAGGACTATAATT | 51433 |
rs551221870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320635 | TTGGGACAGAGTCTC[A/G]CTCTGTAGCCCTGCT | 51433 |
rs551223853 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328954 | CTATCATGAGCAACA[A/C]AATTATCTTGTCATT | 51433 |
rs551252032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337078 | CAAAAATTAGCTGGG[C/T]GTGGTGGCACGTGCC | 51433 |
rs551276951 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319939 | ACACATATTCTTTTT[G/T]GGGGGGATTTAAAAT | 51433 |
rs551287239 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328065 | AACCCTGGTTTACTC[C/T]CCCAGCATGGAGATC | 51433 |
rs551333341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314062 | ATGTGAAATTTACTC[C/T]AGGAATGCAAGGTAG | 51433 |
rs551367701 | in-del | -/TG | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340723 | CACCCGGCTAATTTT[-/TG]TGTGTGTGTGTTTTT | 51433 |
rs551450270 | snp | A/C/G | 3.29468e-05 | 0.00405861 | missense | ANAPC5 | GRCh38.p7 | 12:121308602 | AGAGTCTGGCCTGGA[A/C/G]GTAAACGACGTCCCT | 51433 |
rs551538264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314836 | GGGTTTCACCATGTT[A/G]TCCAGGCTGGTCTCG | 51433 |
rs551591680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341272 | ATCGAGAGTTCAAGA[C/G]CAGCCTGGCCAATGT | 51433 |
rs551871564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312055 | GAACACTTTCCAGGA[C/T]AGACTGTGTTTGGGC | 51433 |
rs551911299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349007 | CAGTGGCTCACGCCT[A/G]TAATACCAGCGCCTT | 51433 |
rs551932002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319103 | GTATGTGAGCATGCT[A/G]TGTATACACAAACAC | 51433 |
rs552025738 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328706 | GAGGCAGAGGGTACA[C/T]GGGAAAGAGCCAGCA | 51433 |
rs552084932 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121356155 | TCTCACTGTGTTGCT[C/T]AGGCTGGTCTGTAAG | 51433 |
rs552135290 | snp | C/G/T | 3.33401e-05 | 0.00408279 | missense | ANAPC5 | GRCh38.p7 | 12:121319800 | CAAACTGTATTTTTT[C/G/T]ATCACATAGCATCCA | 51433 |
rs552146314 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355200 | AGCTTCACTTGAAAA[A/T]TTTGAAAATTTGGTA | 51433 |
rs552183268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340007 | TCAGCCTCTGAAGTA[G/T]TCCATAGCTTTTATG | 51433 |
rs552321406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325853 | GACTGGGCGACAGAG[C/T]GACACTCCGTTTCAA | 51433 |
rs552359375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309996 | CATGTACTACGTTAA[A/G]ACAGGAACCACATTC | 51433 |
rs552385539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340560 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTTTGTC | 51433 |
rs552422836 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323689 | GTCTCAATCCTTTCA[G/T]GAGGTAATGCACTTT | 51433 |
rs552438578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333038 | ATATTATTTGTGGCC[A/G]GGCGCAGTGGCTCAC | 51433 |
rs552470869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331757 | ATATTTTACTTTTCA[C/T]GGCATTCTCTCCTAC | 51433 |
rs552549189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310704 | TTTGGGAGGTGCAGG[C/T]GGGCAGATCACTTGA | 51433 |
rs552581046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330790 | GAATCCTCTCAAATA[A/C]TCTTTCAAGAAATAT | 51433 |
rs552714416 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342833 | CACTGCACTCCAGCC[G/T]GGCGGCAGAGCGAGA | 51433 |
rs552718691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336668 | CTGGGCAACAAGAGC[A/G]AAACTCAGTCTCCAA | 51433 |
rs552783760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317283 | TTTGAGATGGAGTCT[C/T]GCTCTGTTGCCCAGG | 51433 |
rs552965411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322100 | CGATCTCATGACCTC[A/G]TGATCCGCCTGCCTC | 51433 |
rs552974740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350492 | CGAGACCATCCCGGC[C/T]AACACGGTGAAACCC | 51433 |
rs553125137 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316584 | TAAAAATACAAAAAA[A/G]TAGCTGGGCGTGGTG | 51433 |
rs553137977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315007 | AAGAAATACAGGGCA[C/T]CTAAGTGGGAATGGA | 51433 |
rs553214747 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342816 | GCGAGCCAAGATCAC[A/G]CCACTGCACTCCAGC | 51433 |
rs553402218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342156 | GATGGATTCTTGTAT[A/C]GAAAGAGTTCAAAAA | 51433 |
rs553511465 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355653 | CACTTTGAGGCCAGG[A/G]GTTTGACACATGCCT | 51433 |
rs553637550 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121328416 | GGTCGGAGTCCTTTA[A/G]GGCATCCATCAGCTT | 51433 |
rs553697046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327755 | TCCAGGATTAAAATG[C/T]GGCAACAAAGTTTAC | 51433 |
rs553702614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341519 | AGAGAAGTGTTTGGA[A/G]CAAAGTGTATTAATA | 51433 |
rs553702841 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324382 | AAGGCAGCTACCTTC[C/T]AGTTGTGTACTAAAA | 51433 |
rs553783912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334019 | AGTGGCTCATGCTTG[C/T]AATCCCAGCACTTTG | 51433 |
rs553801748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318782 | TCCCAGCACTTTGGG[A/G]GGCCGAGGCGGGCGA | 51433 |
rs553817330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348820 | ATGTGGATAACCCAG[C/T]AATTGCACTTCTAGG | 51433 |
rs553845332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333377 | CCAGAAGGCTGTGTA[C/T]AAATTTCTAACCCCC | 51433 |
rs553911284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326034 | CCCAGGGGAAGCAAC[C/T]AGCTAGCCCTTTCGA | 51433 |
rs553923852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313086 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCGGATG | 51433 |
rs554040384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312290 | AGACTCTGGCTGGGC[A/G]CAGTGGCTCATGCCT | 51433 |
rs554055780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326688 | CCCATGAAGTGGATT[C/T]TATGAGACAGTACCC | 51433 |
rs554061441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310156 | TTCTGAGGGGTTGAA[C/G]TAGGTGGGAGAAAGG | 51433 |
rs554173838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309591 | ATATATTTGTGAACA[C/T]TCAGAACTTAAATGC | 51433 |
rs554216067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353335 | ATACCCTGAATTATT[A/G]TTAATGATCTGGTAT | 51433 |
rs554640281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324729 | TAGAAAGATTCCATC[C/T]CTAAGAAACAAGAAT | 51433 |
rs554712617 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339053 | AATATGACTTTTTTT[C/T]CTTTTTTTTTTTTTT | 51433 |
rs554753060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351612 | ACAGGTGCCCGCCAC[C/T]ACGTCCAGCTAATTT | 51433 |
rs554770364 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331961 | ATGGACCTCAGCCTC[C/T]TGAGTAGCTGGGACT | 51433 |
rs554828211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331284 | ACAACCCAATTCAAC[A/G]GGGCCTTGTGAAGGC | 51433 |
rs554906898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337180 | CCAAGGTCGTGCCAC[C/T]GCACTCCAGCCTGGC | 51433 |
rs554957642 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322064 | AGAGACAGGGTTTCA[A/C]CATGTTGGTCAGGCT | 51433 |
rs554969781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329976 | AATTCACGGCCTTCC[C/T]TATCACTCAAAACGA | 51433 |
rs555069621 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331934 | GCAGCCTTGAATTCC[C/T]GGACTCAGGCGATGG | 51433 |
rs555108332 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329204 | TGTCGCCCAGGCTGG[A/T]GTGCAGTGCAGCAAT | 51433 |
rs555117962 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307910 | AGCCAACATCTAGAA[A/G]GGGACTGAAAAATGC | 51433 |
rs555118012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316455 | ACAGGTATTCAACCC[C/T]GGGCGCGGTGGCTCA | 51433 |
rs555221388 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350203 | AAATACAAGTGATAA[A/C]TTTTTTAAAAAAGCC | 51433 |
rs555260669 | in-del | -/TGTT | 0.0024671 | 0.0350352 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331842 | AATCACTTTTATGTT[-/TGTT]TGTTTGTTTGTTTTT | 51433 |
rs555290043 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323757 | ATTTGAAGTGAATAA[A/G]CAGAAATTACATAGA | 51433 |
rs555447832 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337594 | TGCTCTCCTCTTGAC[C/T]ATCTACAACACTGTT | 51433 |
rs555550632 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349586 | AAATTAAAAAAAAAA[A/T]AAATTTAAAAATAAA | 51433 |
rs555568383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328228 | CCAAGGCAGGTAAAT[C/T]TTGTATGTATGGCCT | 51433 |
rs555650057 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326949 | CTCCACCCTTGGTCC[C/G]CTTCCACTGGTGGGA | 51433 |
rs555765912 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334270 | GGTGACTGAGTGAGA[A/C]CTTGTCTCTTAAAAA | 51433 |
rs555828667 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325088 | AGGATCACTTGAGCC[A/C]AGAAGGTTGAGGCTG | 51433 |
rs555835653 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327494 | GATCCCCCCGCCCCC[A/C]CCCCATGTTCCCTGC | 51433 |
rs555870921 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355897 | TATTTAGGGCATGCC[A/G]TTTCCAACTCACTAC | 51433 |
rs556134887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348704 | AGGAATAAAGAGTAT[A/G]CAACCTCAGCTACCA | 51433 |
rs556135008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340831 | TCCCAAAGTGCTGGG[A/G]TTACAGGCGTGAGCC | 51433 |
rs556138883 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355450 | TAATCCCAGCTACTC[A/G]GGGGGCTGAGGCAGG | 51433 |
rs556145445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348016 | AAGGATTTTTCTATC[A/T]ACCTAAAACACTAAA | 51433 |
rs556245157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312138 | CCTCTGATCACATTA[A/C]ATCAAAAATCAGTAA | 51433 |
rs556247893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332853 | ATAATATTGTAAACA[C/T]AGACAAATTCTGAGA | 51433 |
rs556306276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319166 | GAAAAATTCTGGAAT[C/T]ATAGATAACAGCATG | 51433 |
rs556420425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318685 | AATTTATTCAATTGC[A/G]CTATAAACCTCCCAA | 51433 |
rs556530832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309465 | GTCTTTAACTCCTGA[C/T]TTCTAGCCTGGTACT | 51433 |
rs556564593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316665 | ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 51433 |
rs556566651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323488 | TGCCACCACACACCA[C/T]ACCCAGCTAATTTTT | 51433 |
rs556672501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353023 | TTAAACTCAAATGTT[C/T]AGGAGTTTAACTCTG | 51433 |
rs556782030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331086 | TGCCAGTGCTAAATG[G/T]GATAAAGGTTTCTCT | 51433 |
rs556833166 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308888 | GCGAAGTGGCTCATG[C/T]CTGTAATCCTAGCAC | 51433 |
rs556892769 | snp | C/T | | | missense | ANAPC5 | GRCh38.p7 | 12:121318502 | AAGAGACCCCTTACC[C/T]GATCACCATTTCTGT | 51433 |
rs557016359 | snp | C/G/T | 0.00319098 | 0.0398384 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341157 | GACAGAGTGAGACTC[C/G/T]GTCTCAAAAAAAAGA | 51433 |
rs557023640 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316136 | AACAGGTAAAGGATC[A/G]GAATAGACGTTTCTC | 51433 |
rs557082394 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330330 | GTTGCTCAATAAACT[A/G]AACAATGATCTCTTA | 51433 |
rs557124923 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307793 | CCCCCTTAATTTATA[A/C]TCACCTTACTCATGA | 51433 |
rs557137361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315837 | ATAAGCATTAAAACT[A/G]TAATACTGTGAGAAG | 51433 |
rs557201124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337449 | ATAAACATATGAAAA[A/G]ATATACTAACTAGCA | 51433 |
rs557287614 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337202 | AGCCTGGCAACAGAG[-/T]TAAGACTCTGTTTCC | 51433 |
rs557408041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350345 | ATCACTGTTACTCAA[C/T]AGACAATGCTTATCC | 51433 |
rs557473705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349461 | GCTACTTAGAAGACT[A/G]AGGTAGGAGGACAGC | 51433 |
rs557484057 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348979 | CATTAAAAAGACCAT[C/T]TGGGGCCTGGCGCAG | 51433 |
rs557610611 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341597 | AATAGAGAGTGGTTA[C/G]ATAAGTAATAAATAG | 51433 |
rs557623945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321217 | TCGTGCCATTGCACT[A/C]CAGCCTAGGCAACAA | 51433 |
rs557637572 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334972 | TATTTAGGCAGAAGG[C/T]TTTCATAAACTGTTC | 51433 |
rs557677002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320768 | CCACCATGTCCGGCT[A/G]ATTTTTTTGTATTTT | 51433 |
rs557685227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329310 | AGGCGCCCACCACCA[C/T]GCCCGGCTAATGTTT | 51433 |
rs557689448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328631 | AAAGGAAAGTACCTA[C/T]AACCTGGCCTTAACC | 51433 |
rs557720855 | snp | C/T | | | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335612 | AGCCCTCTTCCCCAT[C/T]ACTTTTGCTTTCGGC | 51433 |
rs557767539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327471 | ACAGCTGGGAGTACA[C/T]GCTCCCAGATCCCCC | 51433 |
rs557813045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342200 | CTCAGAACTAGGAAA[A/G]AAAAACATAAAAAGT | 51433 |
rs557827042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326788 | ACTTCTATTATACTC[C/T]CCTCTCTCCTAAAAC | 51433 |
rs558328929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310453 | CTGCAGTCCCAGTTA[C/T]TCAGGAGGCTGAGGC | 51433 |
rs558391828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318078 | CTCAGGAAAGCCAGT[A/G]CCACTGGAAAGTGTC | 51433 |
rs558569469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311070 | ATGCTGTCTACAAGA[A/G]ACTCACTGTAGATTA | 51433 |
rs558581024 | snp | C/T | 0.000296545 | 0.0121731 | missense | ANAPC5 | GRCh38.p7 | 12:121318564 | TTTTGTAAAAGCTTA[C/T]GTGCCTCTGACATTT | 51433 |
rs558603759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353470 | GTTTTGAGACGGAGT[C/T]TCCTCTGTCGCCCAG | 51433 |
rs558650215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338574 | AGCCTGGGTGACAGG[A/G]CAAGACTCAGTCTCA | 51433 |
rs558673501 | snp | A/G | 1.71849e-05 | 0.00293124 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352344 | GACGCTGGCCATGGC[A/G]GCCCGAGACTAAGTC | 51433 |
rs558813833 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337526 | CCCTCATCTCGCCAG[C/G]CTTGGCTGGCCTTCC | 51433 |
rs558820100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339362 | GGCCTGAAAATGTGA[C/T]TTCTAAACCAAAACC | 51433 |
rs558824345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324905 | AAAAAATACGCTGGG[G/T]GTGGTAATCCCAACA | 51433 |
rs558890066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332772 | AGGAATTAAGGAAAA[C/T]GTACACATTAATAAA | 51433 |
rs558891705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323834 | CACCAATTATTTTCA[C/T]GACCGCCACAGGGAG | 51433 |
rs558902342 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332072 | ACTTCTGGCCTCAGG[C/G]GATCCTCCTGCCTCA | 51433 |
rs558945021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316606 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCACCT | 51433 |
rs558977868 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319318 | GCTCACTGCAACCTC[C/T]GCCTCATGGGTTCAA | 51433 |
rs559090119 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309387 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 51433 |
rs559125751 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316028 | AACAGGAGAAAATAT[G/T]TGTAAATTATATATC | 51433 |
rs559181777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321479 | CTCATCTCAGCCTCC[C/G]GAGTAGCAGGGAATA | 51433 |
rs559202764 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349742 | TTTTTTTTTTGGAGA[C/G]GGATGCCCAGGCTGG | 51433 |
rs559203857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335899 | CAGCTTCAAGACACA[C/T]TCCCCCTAGAGGGAG | 51433 |
rs559397774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314622 | CAAAATAAGGACATA[C/G]ACTTTTTTTTTTTTT | 51433 |
rs559409877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320893 | CAGGCGTGAGCCACC[A/G]TGCCTGGCCAGAGAC | 51433 |
rs559431740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342362 | CACATCCACATGCAA[A/T]AGCATGAAGGTGGAT | 51433 |
rs559486273 | snp | A/G | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307805 | ATAATCACCTTACTC[A/G]TGATGAATTCCTGGA | 51433 |
rs559555648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312794 | CTGAGGCAGGAGAAT[C/T]GTTTGAACCCAGGAG | 51433 |
rs559612124 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313347 | AAAAGAAAGAAACTA[A/G]AAAACGAAAAGCAAA | 51433 |
rs559657516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341749 | CAGGGTTTTAGGCTG[C/T]TAGTCACATACCATT | 51433 |
rs559663237 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310535 | GCCACTGCACTCCAG[C/T]CTGGGCAACAGAGCA | 51433 |
rs559868718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326195 | ACATGTTTGCTATAG[A/G]GAAGTATGTCTAGAC | 51433 |
rs559899208 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321834 | TGAGCCAATGTGCCC[A/G]GCTGACAAATTACTT | 51433 |
rs559978894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340867 | GCCCAGCCTCCATCA[C/T]TTTTGTCTAGATATA | 51433 |
rs559991136 | snp | A/G | 1.75881e-05 | 0.00296543 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121319699 | CAAGGTTTCTTACCT[A/G]TAAACACCCTCTATG | 51433 |
rs560043545 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340532 | CTGCAGAGGTAATTC[C/T]GTAAATTTTTTTTTT | 51433 |
rs560097160 | snp | A/G | 5.23437e-05 | 0.00511557 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327074 | TTGCTCCAGAAGCAC[A/G]TGGGCCCGGCCACCT | 51433 |
rs560221009 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332918 | TTTGGGAGGCCAAGG[C/T]GGGAGGATCACTTGA | 51433 |
rs560221687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353734 | CGTGAGCCACCGCGC[C/T]CGGCCTGCCTTGTGC | 51433 |
rs560238885 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320139 | TAGGCACTCAATTTG[G/T]TATTTATCATTCTCA | 51433 |
rs560276358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333757 | ACTTACTTACCAGCT[C/G]TCAATCTTCTCCCGT | 51433 |
rs560333511 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340519 | GTTTGAAATTCATCT[A/G]CAGAGGTAATTCCGT | 51433 |
rs560497604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338423 | TGAAACCCTGTCTCT[A/G]CTAAAGATACAAAAC | 51433 |
rs560521890 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326325 | AAGAGAAAAATATGA[C/T]CAAGGAAACATCTGG | 51433 |
rs560566370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318199 | AACTCATTATTATCC[C/T]TTCAATACTCAAACG | 51433 |
rs560631020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325191 | AAACTGGCTGGGCGC[A/G]GTGGCTAACGCCTAT | 51433 |
rs560654969 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316748 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAGAAAAC | 51433 |
rs560669060 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308066 | GGCCTCAGAAGAAAG[A/T]CCAAGCCTCATACAG | 51433 |
rs560734046 | snp | G/T | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355963 | TTCTGTTTTGTTTTT[G/T]GGAGCCAGGGTCTCA | 51433 |
rs560781041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316226 | TTAGAGAAGTGCATA[C/T]CAAAACCACAATGAG | 51433 |
rs560869134 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317693 | ATTTTTTAAATCTCC[A/G]CAATAATTCTAATGT | 51433 |
rs561004097 | in-del | -/TAA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344139 | AGTCAGGCACTCTAC[-/TAA]TAAACACTGGGGAAA | 51433 |
rs561034773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330421 | TACCACACAGAATTT[A/T]GTGGTCTGATTAATA | 51433 |
rs561071764 | snp | A/G | 0.000780132 | 0.0197347 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351142 | TCTGGGAGACCAGAC[A/G]GGAGGATTGCTTGAG | 51433 |
rs561103720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322961 | ACCCAGGAGGCAGAG[C/G]TTGCAGTGAGCTGAG | 51433 |
rs561287788 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350403 | AAGAAATCCTCGGGC[A/C]GGGCGCGGTGGCTCA | 51433 |
rs561306364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329851 | AACTCCTGACCTCAG[A/G]TGATCCACCCACCCC | 51433 |
rs561354299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336903 | CAATGGGCTGATTCT[A/C]ATTTGCACAGCTACT | 51433 |
rs561354338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344006 | TAGTTAGGGAAGGAG[A/G]AGTAAAACAGCAAAA | 51433 |
rs561418471 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311159 | TAGCTACTTGGGAGA[A/C]TGAGTTGGGAGGATC | 51433 |
rs561429573 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342495 | ACTCTTAGAAGATCT[C/T]CCTTCCACCTGCTAG | 51433 |
rs561493653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320849 | ACCTCGTGATCTGCC[C/T]GCCTCAGCCTCCCAA | 51433 |
rs561553224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349968 | CACCCACCTCAGCCT[C/T]CCAAAGTGCCGGGGT | 51433 |
rs561555287 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325845 | GCACTCCAGACTGGG[A/C]GACAGAGCGACACTC | 51433 |
rs561561263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341649 | ATCGAGGTAATAGGT[A/G]TGGGTAATTACCATA | 51433 |
rs561636454 | snp | C/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313656 | AGATAAAAGGTAAAA[C/T]GAACAAATTCCTAGA | 51433 |
rs561694277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341144 | CTCCAGCCTCAGTGA[C/T]AGAGTGAGACTCCGT | 51433 |
rs561727950 | snp | C/T | 1.65282e-05 | 0.00287469 | missense | ANAPC5 | GRCh38.p7 | 12:121309821 | TGGGCTCGATGGCCA[C/T]GTGGAGAAGACTTAA | 51433 |
rs561802027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320518 | ATCCACACCTGCTGT[A/G]CCATGCACAGATGGT | 51433 |
rs561837775 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312519 | AGACCATCCTAACAC[A/G]ATGAAACCCCAGCTC | 51433 |
rs561850208 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319518 | GGATTACAGGTGTAA[A/G]TCACCATGCCCAGTT | 51433 |
rs561860437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348991 | CATTTGGGGCCTGGC[A/G]CAGTGGCTCACGCCT | 51433 |
rs561863689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327960 | CACAGAGCAGAGGAG[C/G]CCGGTGCTTGGAGTC | 51433 |
rs561882469 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353512 | GTGGCGCGATCTCTG[C/T]TCACTGCAAGCTCTA | 51433 |
rs561896279 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315635 | CCTATATATCTACGA[A/T]CAGTTGTTTTCTTTT | 51433 |
rs561911996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318891 | TGGGCGTAGTGGTGG[A/G]CACCTGTAATCCCAG | 51433 |
rs562077568 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354950 | ACTGTAAATTGGTAA[C/G]ACTTTCAAGCCATTG | 51433 |
rs562123478 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335173 | CTTTATTTATTTTTT[A/C]TTTTTTTTTGAGACG | 51433 |
rs562286226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325728 | AAAAATTAGCTGGGC[A/C]TGGTGGTGGACACCT | 51433 |
rs562387164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326106 | ACCAGCTGGCAAAGG[C/T]GCCGTGGAACCCATC | 51433 |
rs562662823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345743 | GGGTAAAAAGGGCAT[A/C]AGCCAGCACGTGAAT | 51433 |
rs562690913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353553 | TCACGCCATTCTCCT[A/G]CTTCAGCCTACCGAG | 51433 |
rs562731024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310547 | CAGCCTGGGCAACAG[A/G]GCAAGACTTTGTCTC | 51433 |
rs562743220 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331249 | TTTTGCTGCTGAAGA[-/T]TCTCTGCTCCAACTG | 51433 |
rs562868888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344193 | GGTCTCAGTTCTCAA[A/G]GGGTGAAGAGGCAGG | 51433 |
rs562872087 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329918 | CCACGCCCAGCCAGA[G/T]AAGCCTTTTCAATGC | 51433 |
rs562891014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338348 | TAATCCCAGCACTTT[A/G]GGAGGCCGAGGAGGG | 51433 |
rs562935358 | snp | A/C | 0.000207061 | 0.0101729 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351084 | CAAAATGAAATAACA[A/C]ATGACGGCCGGGCGC | 51433 |
rs563045060 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322144 | GCTGGGATTACAGGC[G/T]TGAGCCACCGCACCT | 51433 |
rs563051284 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354410 | CCTCCCAAATTGCTA[C/T]GATTAAAGGCATGGG | 51433 |
rs563112011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337770 | CCCTCCATGCTCCCA[G/T]AAGCCCTCTGCACTT | 51433 |
rs563478465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336820 | GCCCGAGGAGGGAGG[C/G]AGGAGCTTTGCAACC | 51433 |
rs563507495 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345662 | GCCTCCCATTGGCCA[A/G]TCACAAGTCAGAGGG | 51433 |
rs563540140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338445 | ATACAAAACATTAGC[C/T]GGGTGTGGTGGCGCA | 51433 |
rs563547480 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319217 | TACTTATTTTCTTCA[-/T]TTTTGCTTATCTGTA | 51433 |
rs563568114 | snp | C/T | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308096 | GACCTGCACTGACCA[C/T]CCTGGAGAGATCTAC | 51433 |
rs563657259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336084 | CCTAAAACCTGAATT[C/T]ATATACAAATTATAA | 51433 |
rs563755645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314467 | TGCAGAAAAAAAAAA[A/T]TTGACAAAATCCAAT | 51433 |
rs563861632 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349018 | GCCTGTAATACCAGC[A/G]CCTTGGGAGGCTGAA | 51433 |
rs563972227 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | ANAPC5 | GRCh38.p7 | 12:121320413 | CTATTAGGCGGAAAT[C/T]GTTCCTTCAAGTGCT | 51433 |
rs563995826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313512 | TGATAAACTGTTAGA[C/T]TGACCAAGAAAAAAG | 51433 |
rs564070027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347522 | TGTAGTCCCAGCTAC[C/T]TGGGAGTCTGAGGTG | 51433 |
rs564143125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340597 | GCCAGAGTGCAGTAG[C/T]GCAATCTTGGCTCAC | 51433 |
rs564262788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341009 | TGTTTCCAAGAAAAT[A/G]AAAAAATATGGCTGA | 51433 |
rs564286110 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313334 | TCCATCTCAAAAAAA[A/G]AGAAAGAAACTAGAA | 51433 |
rs564305256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325378 | TGAGGTAGGAGAATC[A/G]CTTGAACCCAGGAGG | 51433 |
rs564509542 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322154 | CAGGCGTGAGCCACC[A/G]CACCTGGCCTGTTTT | 51433 |
rs564607412 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ANAPC5 | GRCh38.p7 | 12:121308396 | AGATAGGGTGTCACA[A/G]ATACATCATTTATAG | 51433 |
rs564693599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314127 | AAAATCGGGGCTGGG[C/T]GCAGTGGCTCACGCC | 51433 |
rs564706768 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334081 | AGGAGTTTGAAACCA[G/T]CCTGGGTAACAAAGC | 51433 |
rs564743843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345590 | ACCCCCAAGAAAGGG[A/G]GCCAATGAATCCACA | 51433 |
rs564832955 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309540 | TCTGCCAAGCATGCA[-/T]GTGAAAGCACTTTAA | 51433 |
rs564840462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339715 | CTCAAATGATCCACC[C/T]GCCTTGGCCTTCCAG | 51433 |
rs564840965 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343612 | ATGAGTTTTGGGGAG[C/T]AGTTAATGGTACTAT | 51433 |
rs564852419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346346 | TGGCTCCCCCAACCA[C/G]AGGTAATCTCCATAA | 51433 |
rs564968446 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309025 | GTGGTGGCAGGCACC[C/T]GTAATCCCAGCTACT | 51433 |
rs565004371 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352442 | CCCGCCCTCACAATA[A/G/T]CCCAGGAAACAGACA | 51433 |
rs565033515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316795 | GCTGTACAGAAATGT[A/G]AAGAGCCGCTATTCA | 51433 |
rs565122141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317442 | TATTTTTAATAGAGA[C/T]GGGGTTTCACCATGC | 51433 |
rs565156769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350834 | CTGGTGGAGGTTACC[C/G]TCTAATGGGAGAGAA | 51433 |
rs565187522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323001 | CTGCACTCCAGCCTT[C/G]GCCCCAGAGCAAAAC | 51433 |
rs565252311 | snp | A/G | 1.72166e-05 | 0.00293394 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331318 | TTCAACCCGTGAACA[A/G]AACTCCCAAGACCAG | 51433 |
rs565282028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337708 | TAGCTCATCCTCTGG[A/G]CCACCTGCTTCTGTC | 51433 |
rs565362744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338242 | TAATTTCTTTAAAAA[A/G]AATTTTTTTAAAGTA | 51433 |
rs565363127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330468 | ACTGCCAAGAATAAA[A/G]CCACACTTTGAAACC | 51433 |
rs565537825 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308004 | AACAAGTCCTCGTGA[C/G]CAGCCACAGGAACCA | 51433 |
rs565600561 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317400 | CTGGGATTACAGGCA[C/T]GTGCCACCACGCCCG | 51433 |
rs565623457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328029 | AACTGCGTTTGCGAT[C/T]GCGGGTAGATCAGAT | 51433 |
rs565648083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313866 | TCCCAGAAAAAGGAG[A/T]AGAGAGAATACTTTC | 51433 |
rs565689180 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336605 | AATCACTGAGAACCC[A/G]GGAGGCAGAGGTTGC | 51433 |
rs565697059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334706 | GCAGCCTGAATTCTA[C/T]CTGAAAGCAAACCTG | 51433 |
rs565708849 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320620 | CTTTCTTTTTTTTTT[G/T]TGGGACAGAGTCTCG | 51433 |
rs565841511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313097 | TTGGGAGGCCAAGGC[A/G]GATGAATCACCTGAG | 51433 |
rs565842400 | in-del | -/CCACGT | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351610 | TACAGGTGCCCGCCA[-/CCACGT]CCACGTCCAGCTAAT | 51433 |
rs566075296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348656 | GGCGACAGAGCAAGA[C/G]TCCGTCTCCAATAAA | 51433 |
rs566247479 | snp | A/T | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354336 | TGTAGACACGAGGTC[A/T]TGCGATGTTGTCCAG | 51433 |
rs566254704 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318963 | AGGCAGAGATTGCAG[G/T]GAGCTGAGATCGTGC | 51433 |
rs566259298 | snp | C/T | 6.59642e-05 | 0.00574262 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347885 | AATATCTGGGCCCTG[C/T]GTAAAGGAGAGATAG | 51433 |
rs566283257 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355077 | GTTGCAAACTGAAGT[G/T]GCAATCTAAACTAAA | 51433 |
rs566533651 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318203 | CATTATTATCCTTTC[A/G]ATACTCAAACGTAGT | 51433 |
rs566618932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333018 | AAGAAATTCTGTTCA[G/T]CAAAATATTATTTGT | 51433 |
rs566692810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339140 | GCTCACTGCAACCTC[C/T]ACCTCTCAGGTTCAA | 51433 |
rs566692952 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315474 | GCAAGGGATGCTGAA[C/T]AGCCAAAACAATCCT | 51433 |
rs566729917 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309639 | CTTTTCTTCTTCTGG[A/G]TCCTAAACTTTCAAT | 51433 |
rs566749101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345132 | GGAGGAAGGACTGAC[C/T]GGATCTGCTGAGGGA | 51433 |
rs566792082 | snp | A/G | 8.23744e-05 | 0.0064172 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345907 | ACTGGTCAGTTCCAT[A/G]TCAGCATCCTCCACT | 51433 |
rs566805271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331626 | GGAAATATAGGACAT[A/G]TCTCTTCTAAGGGGA | 51433 |
rs566805833 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338514 | GAATCACTTGAACTC[A/G]GGAGGCAGAGATTAC | 51433 |
rs566853679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352624 | CCAGGCTACGTGGAC[A/G]GGGACCGGATGGGAG | 51433 |
rs566879705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337833 | AATTGCCAATCTGAC[A/C]CCACCCCAGACTGTA | 51433 |
rs566894977 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351461 | CGTCCTTGGCTTTAT[A/G]CCTTTTTTTTTTTTG | 51433 |
rs566905738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309952 | CAGTTCTCTCCTGAA[C/T]GGCTATCTCTGGCTT | 51433 |
rs566964984 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317064 | GACAGAAACCGGTGA[G/T]AGGTTACCAGAGGCT | 51433 |
rs566980298 | snp | A/G | 0.000399281 | 0.0141238 | missense | ANAPC5 | GRCh38.p7 | 12:121308590 | CCAGGGTATGGTAGA[A/G]TCTGGCCTGGAAGTA | 51433 |
rs566995049 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320839 | CGATCTCCTGACCTC[A/G]TGATCTGCCCGCCTC | 51433 |
rs567025295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323276 | TTTTTGGGCCATGCT[C/T]TCTGTGAATGTACAT | 51433 |
rs567035414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322682 | TACAATGAATATCTT[C/G]GTGCATAGAGCTTTG | 51433 |
rs567042183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316500 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 51433 |
rs567048644 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328932 | ATAGGAGATCAAAAA[A/T]GGATGCCTATCATGA | 51433 |
rs567088624 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332400 | AACCAGAGATTTACA[A/G]ATTGAAGGAGTTGAG | 51433 |
rs567216867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330123 | GGCCACACTTGGTTT[A/C]TGTCACGTATTTCTT | 51433 |
rs567217948 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315715 | GGGAAAGAGGAGTCT[C/T]CAACAAATGGTGCTA | 51433 |
rs567342409 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326407 | CCCTGACTCTTTCCC[A/G]TGAAAGAAGATATTT | 51433 |
rs567345736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350489 | GATCGAGACCATCCC[A/G]GCTAACACGGTGAAA | 51433 |
rs567416454 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314783 | GCATGCACCACCACC[A/G]CTACACTCAGCTAAT | 51433 |
rs567521699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321065 | GACCAGCCTGACCAA[C/G]ATGGAGAAACCCCAT | 51433 |
rs567808850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336193 | TTAATCACTGAAACT[C/T]CCCTAACAGGCAGAT | 51433 |
rs567901250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349063 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGACA | 51433 |
rs568043202 | snp | C/T | 3.93074e-05 | 0.00443308 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352101 | CTCAGTAAAAGTTTG[C/T]TGCACGAGCAGGAGC | 51433 |
rs568043375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348719 | GCAACCTCAGCTACC[A/G]AGAAGATTACAGTCT | 51433 |
rs568073786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340630 | CAACCTCCGCTCACC[A/G]CAACCTCCACCTCCC | 51433 |
rs568132536 | snp | C/T | 1.6743e-05 | 0.0028933 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327255 | GGAGAGGGAACAGGA[C/T]TTCCTTTCAGCAGCA | 51433 |
rs568138460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347643 | CTCCAAAGAAAAAGC[A/T]ATCCATTTTTCAACA | 51433 |
rs568155935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313051 | AGAAAAGAGGCCGGG[C/T]GCGGTGGTTCACGCC | 51433 |
rs568168287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319915 | TAGCAAATATCCTTA[C/T]AATAATTCACACATA | 51433 |
rs568230888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319168 | AAAATTCTGGAATTA[C/T]AGATAACAGCATGTT | 51433 |
rs568388029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333950 | ACTGTTCCCTCCCCA[C/T]ACAAGCTTCAGCTTG | 51433 |
rs568542840 | snp | C/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355153 | AACACTTAAAAATTA[C/G]GATATTTCTGCCAAC | 51433 |
rs568619068 | snp | C/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355088 | AAGTTGCAATCTAAA[C/G]TAAATGCGGCTCATT | 51433 |
rs568637035 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354194 | GGGTTTCACCATGTT[G/T]GCCCGGCTGGTCTTG | 51433 |
rs568689497 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327738 | TGAGGTAGCGACAGA[A/C]CTCCAGGATTAAAAT | 51433 |
rs568726272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323869 | GCATGGGGATATAGA[A/T]CCTGCAGTATCCCCC | 51433 |
rs568789469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324593 | TTGAACAAAGTTACA[A/C]GGCTAAAGAATTGAG | 51433 |
rs568808349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310755 | CCTGGCCAACATGGT[A/G]AAACCCTGTCTTTCC | 51433 |
rs568842927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323507 | CAGCTAATTTTTGTA[C/T]ATTTTGTAGAGACGG | 51433 |
rs568906270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331900 | AGGTTGGAGTACAGT[G/T]GCACAATCCTAGCTC | 51433 |
rs569001878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339042 | TCTCATCATCAAATA[C/T]GACTTTTTTTTCTTT | 51433 |
rs569032685 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338481 | GTAATCCTAGCTACT[C/T]GGGAGGCTGAGGCAG | 51433 |
rs569124210 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308322 | AAAGGGGAATAAAAC[A/C]AATACGTAGTTACTA | 51433 |
rs569157030 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351467 | TGGCTTTATGCCTTT[A/T]TTTTTTTTGAAACGG | 51433 |
rs569168211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352188 | CTCCATGAGGCTGAC[C/G]GCGCCCTCGCCTGTG | 51433 |
rs569170162 | snp | C/T | | | missense | ANAPC5 | GRCh38.p7 | 12:121318392 | GTAGGGGAGGAAGAT[C/T]GCCAGTACAGCTCTG | 51433 |
rs569209146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344390 | TTGAGACCAGCCTGG[C/G]CAACACAGTGAAACC | 51433 |
rs569309892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350477 | ACGAGGTCTGGAGAT[C/T]GAGACCATCCCGGCT | 51433 |
rs569311798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342754 | GTCCCAGCTACTCAG[G/T]AGGCTGAGGCAGAAA | 51433 |
rs569368338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329967 | GAGGACTATAATTCA[C/T]GGCCTTCCCTATCAC | 51433 |
rs569417106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315840 | AGCATTAAAACTATA[A/C]TACTGTGAGAAGAAA | 51433 |
rs569488080 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351843 | CTCCAACGCTCTATT[G/T]TATAGCCCCATTTTA | 51433 |
rs569592003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321032 | AGACGGGTGGATCAC[A/C]TGAGGTTGGGAGTTC | 51433 |
rs569622980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336509 | ATGGTGAAACCCCGT[C/T]TCTACTAAAAATACA | 51433 |
rs569670728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328086 | CATGGAGATCACCCA[C/T]CCATTACCTCACAAA | 51433 |
rs569717282 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314863 | CTCGAACTCCTGGCC[A/T]TAAGTAATCTGCCTT | 51433 |
rs570077136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341863 | CGTTAGTGAGGCAGA[G/T]GGGACCAAGAGTAAA | 51433 |
rs570129696 | snp | C/T | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355712 | TAAAAATACAAAAAT[C/T]AGCCAGGTGTGCTGG | 51433 |
rs570162456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334869 | TGACCTAATTTCTTT[C/T]TCACTGAACGGCCTG | 51433 |
rs570219858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341301 | GTGGTGAAACCCCAT[C/G]TCTACTAAAGATACA | 51433 |
rs570254797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312944 | CAAATTTATGAAATA[C/T]AGTTCTCAAGGAAAT | 51433 |
rs570407986 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328036 | TTTGCGATCGCGGGT[A/G]GATCAGATGTGTGAA | 51433 |
rs570504913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346713 | GACAAAACAGAAGGT[A/G]CTTTTCCACAGTTAA | 51433 |
rs570576327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352764 | TTGTTTGAGACGATA[A/T]CTCGCTATGTTACCA | 51433 |
rs570599233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326450 | AGATAAAGCCTACAG[C/T]AGCAGAAGAGATACT | 51433 |
rs570601277 | snp | C/T | 6.59141e-05 | 0.00574045 | missense | ANAPC5 | GRCh38.p7 | 12:121318575 | CTTATGTGCCTCTGA[C/T]ATTTGGTTCTGAGCT | 51433 |
rs570611838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325896 | CTTCAATATGTTCAC[C/T]GACTCATTCATTACC | 51433 |
rs570745473 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339523 | TCGCACAAGCTGAAG[A/T]ACAGTGGCGAAATCT | 51433 |
rs570786994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324474 | ATAAGCCCAGAGGTG[A/G]AAGGGAGATGAAGAT | 51433 |
rs570863374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331766 | TTTTCATGGCATTCT[C/G]TCCTACATTATTTGA | 51433 |
rs570921136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309394 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 51433 |
rs570925716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310027 | CTAGAAAACACAACA[C/T]GTGACAATCTGATTT | 51433 |
rs571033526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317284 | TTGAGATGGAGTCTC[A/G]CTCTGTTGCCCAGGC | 51433 |
rs571238253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338446 | TACAAAACATTAGCC[A/G]GGTGTGGTGGCGCAC | 51433 |
rs571297945 | snp | A/G/T | 3.29598e-05 | 0.00405941 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308675 | TTCATTGAGGTTCTC[A/G/T]ATGGCAGCCTCCAGA | 51433 |
rs571321422 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342274 | TGCATGGTCAAATGG[G/T]TTTTGGCAACAGTGC | 51433 |
rs571334321 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336986 | ACACTTTGGGAGGCC[A/G]ACGCGGGCAGATCAT | 51433 |
rs571348378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344352 | GGGAGGCCAAGGCGG[A/G]TGGATCACCTGAGGT | 51433 |
rs571381769 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341162 | GTGAGACTCCGTCTC[-/A]AAAAAAAAGAAACAA | 51433 |
rs571517300 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308284 | AAGAAAAAGTTGGTG[C/T]CCTTTGCTACCAAAA | 51433 |
rs571592264 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333707 | GGGAAACTGTTTCCT[C/T]ATAATGAGCAGAAAT | 51433 |
rs571752273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321165 | GAGGCAGGAGAATCG[C/T]TTGAACCCAGGAGGC | 51433 |
rs571876832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342588 | CGAGGAGGCCAAGCG[C/T]GGTGGCTCACACCTG | 51433 |
rs571943287 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329223 | CAGTGCAGCAATCTC[A/G]GCTCACTGCAAACTC | 51433 |
rs572013599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348831 | CCAGCAATTGCACTT[C/G]TAGGGAAGTTATTTT | 51433 |
rs572059411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335037 | GACTAGTCCAGGTTG[A/T]TGAGCTGCTTTCCTA | 51433 |
rs572077031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340919 | AAGCTCATAACAAAA[A/T]TAGGGAAAAGTAGAA | 51433 |
rs572122326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326047 | ACCAGCTAGCCCTTT[C/T]GACCTCAGAAAACAT | 51433 |
rs572132645 | in-del | -/TT | 0.0154538 | 0.0865337 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311030 | ATTGTGAGAACAAAC[-/TT]TTTTTTTTTAAAGTA | 51433 |
rs572234119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312306 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTCT | 51433 |
rs572294585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332919 | TTGGGAGGCCAAGGT[A/G]GGAGGATCACTTGAG | 51433 |
rs572357516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318806 | CGGGCGAATCACAAG[A/G]TTAGGAGCTCGAGAC | 51433 |
rs572403072 | snp | A/G | | | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335591 | CGTATCTCAAGCTCC[A/G]GCCATAGCCCTCTTC | 51433 |
rs572407071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311473 | ACAATTATAAACAAG[A/C]CAAACAACAGTGTTC | 51433 |
rs572449728 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309227 | AGGCTGAGGTGGGCA[A/G]ATCACAAGGTCAGGA | 51433 |
rs572538300 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340217 | CAGCTACTTAGGAGG[C/T]TGAGGCAGGAGAATC | 51433 |
rs572556969 | snp | C/T | 0.000251019 | 0.0112003 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346917 | CACTTGTTTTGTGAA[C/T]CTCTGGTTCAGTTCC | 51433 |
rs572721536 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348644 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 51433 |
rs572837396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318004 | TCTGTGTCAGCTAAT[C/T]ATTAATATGATGCAG | 51433 |
rs572856602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353391 | AAGAAAAACCACATA[C/T]CATTCAACTTTGGCT | 51433 |
rs572943302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317414 | ACGTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 51433 |
rs572953562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323599 | AGCCTCCCAAAGTGC[C/T]GGGATTACAAGTATA | 51433 |
rs572975233 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322967 | GAGGCAGAGGTTGCA[A/G]TGAGCTGAGATCACA | 51433 |
rs573098473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331993 | AGGCACTCACCACCA[G/T]GCTTGGTCGGCTAAT | 51433 |
rs573134451 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311968 | ACTACAAATGAACTG[G/T]CCCTAACATATATAT | 51433 |
rs573199151 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344576 | GTGACAGTGAGACTT[G/T]ATCTCAAAAAAAAAA | 51433 |
rs573209899 | snp | C/G | 8.68802e-05 | 0.00659034 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331310 | AAGGCCAATTCAACC[C/G]GTGAACAAAACTCCC | 51433 |
rs573249307 | snp | C/T | | | utr-variant-5-prime, synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121347807 | TGAAGTTTACCTGAT[C/T]TGCACTGAATTTGCC | 51433 |
rs573277624 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337653 | CCCATCGCTCCCCAG[C/T]CATATACTACCCAAA | 51433 |
rs573337304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350734 | CCACCTCTATCGCAT[C/T]TCATTCATTTTACAA | 51433 |
rs573510864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342282 | CAAATGGTTTTTGGC[A/G]ACAGTGCCAAGACCA | 51433 |
rs573530329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322093 | CTGCTCTCGATCTCA[C/T]GACCTCGTGATCCGC | 51433 |
rs573579983 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329481 | TACATTAAATTACTA[C/T]CTGTAATTACTTTCC | 51433 |
rs573669441 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314226 | CCAACATGGCAAAAC[C/G]CTGTCTCTACTAAAA | 51433 |
rs573779617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313310 | CAGCCTCGGTGACAA[C/G]AGCTAAACTCCATCT | 51433 |
rs573889779 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313035 | TCCACCTTAAGAAAC[C/T]AGAAAAGAGGCCGGG | 51433 |
rs573895637 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342613 | CACCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA | 51433 |
rs573904889 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308924 | GAGGCCGAGGCGGGT[A/G]GATCACCTGAGGTCA | 51433 |
rs573961735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348998 | GGCCTGGCGCAGTGG[C/T]TCACGCCTGTAATAC | 51433 |
rs574109795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327635 | CACACCGTGCCAAAA[A/C]ATTATCTGAAATACA | 51433 |
rs574303185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334944 | TGTTACATAGTGACA[C/T]TAGGGGGCAGACTAT | 51433 |
rs574422374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334364 | AAGGGATAGATGTCT[C/G]CATTATTGAACTGTG | 51433 |
rs574479059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340840 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 51433 |
rs574480744 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321686 | GGAATTACAGGTGCG[C/T]GCCACCATGCTCAGC | 51433 |
rs574493168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340468 | TGTACTTTTTCCTTA[C/G]AGTTAACCAATCACA | 51433 |
rs574559082 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354344 | CGAGGTCTTGCGATG[C/T]TGTCCAGGCTGGTCT | 51433 |
rs574654804 | snp | C/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311391 | GTTTAAGTTAAAAAC[C/T]GTTACAAGAGACAAG | 51433 |
rs574689832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325979 | AGGTGCCAGTGCCAC[A/G]AAGAGGGAAGAAACA | 51433 |
rs574692787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346227 | GTTTCTTCTTATACA[A/G]GGCACAATCTACCCA | 51433 |
rs574703443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345394 | TAACAAAGGATCAAT[G/T]GACAAAAGTAGGGGA | 51433 |
rs574769463 | snp | A/C | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353794 | TCTCTCTCTCTCATT[A/C]TGCTACCGAGGCTGG | 51433 |
rs574796298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332902 | CCTATAATCCCAGCA[C/G]TTTGGGAGGCCAAGG | 51433 |
rs574814884 | snp | A/G | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307994 | GTCAGGGACCAACAA[A/G]TCCTCGTGAGCAGCC | 51433 |
rs574829779 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342589 | GAGGAGGCCAAGCGC[A/G]GTGGCTCACACCTGT | 51433 |
rs574867887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332278 | CAAAGCTAGTTTTAG[A/G]AAGTATTTTGAGGAT | 51433 |
rs574877806 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311268 | CTGTCTCTAAAAAAA[A/T]AAAATAAAGACACAA | 51433 |
rs574994774 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345048 | GAGTAGATTTGGTAG[A/T]GATTGGGTGCTTAGA | 51433 |
rs575054410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322153 | ACAGGCGTGAGCCAC[C/T]GCACCTGGCCTGTTT | 51433 |
rs575099931 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349521 | GCTAGGATCGCACCA[C/T]GGCACTCCAGCCCAG | 51433 |
rs575101181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308779 | AGTTTTATTTGTTCA[A/G]CAACTACCAGAAGAT | 51433 |
rs575115466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351891 | GAGACTCTAACTCTC[A/T]GCTAATAAATACTGG | 51433 |
rs575120387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309476 | CTGACTTCTAGCCTG[A/G]TACTTGGCTCTATAG | 51433 |
rs575134455 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324214 | CTGCAGCTGGCCAAA[-/C]TTAATTTCACAAGTA | 51433 |
rs575309411 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348269 | TGCTTTGTAAACTGG[A/T]AAACACTATACAAAT | 51433 |
rs575354939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331106 | AAGGTTTCTCTTCTT[C/T]CATGGCAAGTTGCAT | 51433 |
rs575370452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330387 | GATGTTATTAGGATA[C/T]AGGGAACAGAGAGAA | 51433 |
rs575485543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337459 | GAAAAGATATACTAA[C/T]TAGCATCACCTGATT | 51433 |
rs575693425 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329054 | TGTAGTTAAGCCTGC[A/G]CTTACTTCAAGGAGC | 51433 |
rs575720911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350598 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 51433 |
rs575767536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342213 | AAGAAAAACATAAAA[A/C]GTGATGTTGAGATCA | 51433 |
rs575781027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350353 | TACTCAACAGACAAT[A/G]CTTATCCATCAAGGC | 51433 |
rs575864138 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315127 | AAGTTTGGCAAAGTT[A/G]CAGGATATAAGATCA | 51433 |
rs575866892 | snp | G/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353254 | TCCCCAGCCAACATT[G/T]TGAACCTGATTTTTC | 51433 |
rs575883712 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336635 | CAGTGAGCCAAGATC[A/G]CACCACTGCACGCCA | 51433 |
rs575921899 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329315 | CCCACCACCACGCCC[A/G]GCTAATGTTTGTATT | 51433 |
rs575928560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314507 | TGAAAAAAACACTAA[A/G]TAAACTAGGAATAGA | 51433 |
rs575982400 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320102 | CTTTGCAAATTCTAC[A/G]TCTCTTTCTCTTTTT | 51433 |
rs576110542 | in-del | -/TT | 0.00358994 | 0.0422147 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345453 | AGTCCCCAGGACTGA[-/TT]TAACAGTGGGGTACC | 51433 |
rs576220120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326083 | GTGCTTCCCAGACAT[A/G]GGAAGAAACCAGCTG | 51433 |
rs576238726 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332022 | ATTTTTTTAAAAATA[C/G]ATATAGAGTCTCACT | 51433 |
rs576340812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312449 | CAGCGGCTCACACCT[A/G]TAATCCCAGCACTTT | 51433 |
rs576371784 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355726 | TTAGCCAGGTGTGCT[A/G]GGATGCACCTGTAAT | 51433 |
rs576504648 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335115 | TTTGAGAATTCATTT[C/T]TTCCATTTCTTTTCC | 51433 |
rs576543628 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333685 | CTTCCTCAGAGGGTT[C/T]AATAAGGGGAAACTG | 51433 |
rs576564094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340714 | GGCATCACCACACCC[A/G]GCTAATTTTTGTGTG | 51433 |
rs576641125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340245 | ATCGCTTGAACCCGG[A/G]AGGCAGAGGTTGCAG | 51433 |
rs576842388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311211 | GTTACAGTGAGCTAC[A/G]ATTGCAGCAATGCAC | 51433 |
rs576889000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345167 | GGTGAAGGACAGGGA[A/G]GAATCAAGGATACTA | 51433 |
rs576952618 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354290 | GGCCTGAGCCACTGT[A/G]CCTGGATGCATGGCT | 51433 |
rs576964295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353483 | GTCTCCTCTGTCGCC[A/C]AGGCTGGAGTGCAGT | 51433 |
rs576981684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317469 | ATGCTGGCCAGGCTG[C/G]TCTTGAACTCCTGAC | 51433 |
rs577000794 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352355 | TGGCGGCCCGAGACT[A/T]AGTCTCGGGCCCGCG | 51433 |
rs577060598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351765 | CCCGGCCCGGTTTTA[C/T]GGCATTTTTACTGTT | 51433 |
rs577067075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318103 | AGTGTCAGTTTGTCA[C/G]CAGGTTCACACCTCC | 51433 |
rs577094144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332811 | TCTCCTCATTTATAT[A/T]CTGTGCAATTAGCTG | 51433 |
rs577129426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324983 | TAGCCTGGGCAACAG[A/G]GTGAGATTCCATCTC | 51433 |
rs577170650 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338621 | CAAAACAAAAAACAA[A/G]TTATTATGTAGGTGT | 51433 |
rs577343850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344625 | AAGTATTTGGGATAG[A/G]CGCTACCTCGTGGTC | 51433 |
rs577507397 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308006 | CAAGTCCTCGTGAGC[A/T]GCCACAGGAACCACA | 51433 |
rs577761607 | snp | C/T | 1.66977e-05 | 0.00288939 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337243 | AAACAAAAAAAGTTG[C/T]CTTGTCATTCCTTTC | 51433 |
rs577773238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343735 | AATGTCACCCCCTGC[C/T]ACCCTGGGGATTACA | 51433 |
rs577805779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338330 | CGTGGTGGCTCACAC[C/T]TGTAATCCCAGCACT | 51433 |
rs577823573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342837 | GCACTCCAGCCTGGC[A/G]GCAGAGCGAGACTTC | 51433 |
rs577981827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312472 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 51433 |
rs577999086 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309924 | CCTTCACCAGGAAGC[A/G]TTTCATTTCTGGCAG | 51433 |
rs578054281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350304 | CCCATAATATAGAGG[C/T]CCAGGGACCCAGATC | 51433 |
rs578065392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314268 | CTTGGGCATGGTGGT[A/G]CACACCTGTGATCCC | 51433 |
rs578100079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349744 | TTTTTTTTGGAGACG[A/G]ATGCCCAGGCTGGAG | 51433 |
rs578256405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327761 | ATTAAAATGCGGCAA[C/T]AAAGTTTACTTCCAG | 51433 |
rs745525334 | snp | C/T | 1.65231e-05 | 0.00287424 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318484 | CATCTCCGTGAGATG[C/T]ACAAGAGACCCCTTA | 51433 |
rs745722244 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313747 | AAAGAGACTGAATTA[A/G]TAACCAAAAAAACTT | 51433 |
rs745817421 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321626 | AACCTCCTCCTCCTG[C/G]GTTCTAGCAATTCTG | 51433 |
rs746013125 | snp | C/T | 1.65116e-05 | 0.00287324 | missense | ANAPC5 | GRCh38.p7 | 12:121309806 | CCCCGTCAGCCAAGA[C/T]GGGCTCGATGGCCAT | 51433 |
rs746040244 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338434 | CTCTACTAAAGATAC[A/C]AAACATTAGCCGGGT | 51433 |
rs746111293 | snp | A/G | 1.8037e-05 | 0.00300303 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318266 | TGCTATAAAAACAGA[A/G]ATCGGCTTACCTGCG | 51433 |
rs746117700 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308333 | AAACAAATACGTAGT[G/T]ACTAGCAACAAAATA | 51433 |
rs746126628 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339780 | ATCCTGTTTGCCTGT[C/T]AATTATGTTAAAACA | 51433 |
rs746190770 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315683 | GTTTTTAACAGGGGT[A/G]CCAAAACCATTAAAT | 51433 |
rs746313112 | snp | A/G | 3.33422e-05 | 0.00408289 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121319801 | AAACTGTATTTTTTG[A/G]TCACATAGCATCCAT | 51433 |
rs746385283 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317825 | TAGGGCCTATAAGGT[A/T]CTAGGGAATATAGAT | 51433 |
rs746487607 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313841 | TTAACACCAATCCTT[C/T]TCAAATTCTTCCCAG | 51433 |
rs746547824 | snp | C/T | 1.66065e-05 | 0.00288149 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318654 | TTTAACTAGTCACTT[C/T]GAGGGTAAGAATCTC | 51433 |
rs746754779 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322899 | GCGCAGTGGCAGGTG[C/T]CTGTAATCCCAGCTA | 51433 |
rs746955839 | snp | C/G | 1.65386e-05 | 0.00287559 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121309825 | CTCGATGGCCATGTG[C/G]AGAAGACTTAAGGCC | 51433 |
rs747222462 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314415 | CACTCTATCTCAAAA[A/T]CAAACAAACAAAAAC | 51433 |
rs747383939 | snp | A/C/G | 3.29485e-05 | 0.00405874 | missense | ANAPC5 | GRCh38.p7 | 12:121308584 | TCTTCCCCAGGGTAT[A/C/G]GTAGAGTCTGGCCTG | 51433 |
rs747451101 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318013 | GCTAATCATTAATAT[C/G]ATGCAGGTGTTCTCA | 51433 |
rs747585181 | snp | G/T | 1.64784e-05 | 0.00287035 | missense | ANAPC5 | GRCh38.p7 | 12:121308665 | AGTTCTTGGCTTCAT[G/T]GAGGTTCTCGATGGC | 51433 |
rs747623732 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317699 | TAAATCTCCGCAATA[A/G]TTCTAATGTACAGCC | 51433 |
rs747641245 | snp | C/T | 1.66907e-05 | 0.00288879 | missense | ANAPC5 | GRCh38.p7 | 12:121319779 | TGCCATCATTCATTG[C/T]TCTGTCAAACTGTAT | 51433 |
rs747715404 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315482 | TGCTGAATAGCCAAA[A/G]CAATCCTGAAAAAGA | 51433 |
rs747738760 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324631 | GCACTGTGACTCACA[C/T]CTGTAATTCCAACAC | 51433 |
rs747862369 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327537 | TTAATTAGTTTTCAC[A/G]GGTGAATTCAGACCC | 51433 |
rs747990086 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338306 | CATTATAGAAAATTA[C/T]TGGCCAGGCGTGGTG | 51433 |
rs748051349 | snp | A/G | | | utr-variant-3-prime | ANAPC5 | GRCh38.p7 | 12:121308390 | TTGACAAGATAGGGT[A/G]TCACAAATACATCAT | 51433 |
rs748066692 | snp | A/G | 1.68386e-05 | 0.00290155 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318382 | CAGCGCGATGGTAGG[A/G]GAGGAAGATCGCCAG | 51433 |
rs748127134 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310160 | GAGGGGTTGAACTAG[A/G]TGGGAGAAAGGTAAC | 51433 |
rs748253170 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343644 | ATCCTCTTGCTCTCA[A/G]TATGTGCTGAACAAA | 51433 |
rs748782549 | snp | C/T | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308068 | CCTCAGAAGAAAGTC[C/T]AAGCCTCATACAGAC | 51433 |
rs748787687 | snp | G/T | 6.59033e-05 | 0.00573997 | missense | ANAPC5 | GRCh38.p7 | 12:121308555 | GAGCATCGCACACCG[G/T]TTCCTCTCCTGGGTC | 51433 |
rs749026756 | in-del | -/TCTT | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320105 | TGCAAATTCTACGTC[-/TCTT]TCTCTTTTTTCAAAG | 51433 |
rs749087930 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310507 | GGTCAAGGTTGCAGT[A/G]AGCCACAATCGTGCC | 51433 |
rs749092418 | snp | A/G | 1.68111e-05 | 0.00289918 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318397 | GGAGGAAGATCGCCA[A/G]TACAGCTCTGCCACG | 51433 |
rs749191943 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334901 | TGTTCTTAGAAGTAA[C/T]GAAAGAGGCTAGGCA | 51433 |
rs749530912 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322383 | AGTCTGGTCTCCAAC[G/T]CCTGACCTCAGGTGA | 51433 |
rs749550358 | snp | C/T | 1.68015e-05 | 0.00289836 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309685 | ATTGCCTAACAGTCT[C/T]CGTACAGCTTCCTAC | 51433 |
rs749575108 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316558 | CTAACACAGTGAAAC[C/T]CCATCTCTACTAAAA | 51433 |
rs749604863 | snp | C/G | 1.64958e-05 | 0.00287187 | missense | ANAPC5 | GRCh38.p7 | 12:121309786 | ACGACCTTTGTCCAG[C/G]ATAGCCCCGTCAGCC | 51433 |
rs750013415 | snp | A/T | 1.6489e-05 | 0.00287128 | missense | ANAPC5 | GRCh38.p7 | 12:121309761 | GGCACTTGGCCACTA[A/T]GAACATGGCACGACC | 51433 |
rs750064426 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337041 | TGGCCAACATGGTGA[A/C]ACCCCATCTCTACTA | 51433 |
rs750117941 | snp | C/T | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307876 | GAAAAAAAAAGTGCC[C/T]ATGCAGAATATATAA | 51433 |
rs750175419 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346506 | TAATAGAAAAGCATC[A/G]AAGAAACACCACGTA | 51433 |
rs750186495 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315020 | CATCTAAGTGGGAAT[A/G]GAAGAGGTAAAACTA | 51433 |
rs750280814 | snp | A/G | 0.000151417 | 0.00869975 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121319747 | TCCTGTAACAAGTGA[A/G]TCAGCCAAATGATAT | 51433 |
rs750318977 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320882 | TGCTGGAATTACAGG[C/T]GTGAGCCACCATGCC | 51433 |
rs750372276 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322441 | TGGGATTACAGGCAT[A/G]AGCCACCGTGTCCAG | 51433 |
rs750382349 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316593 | AAAAAAATAGCTGGG[C/T]GTGGTGGCGGGCGCC | 51433 |
rs750394024 | snp | A/G | 0.000116361 | 0.00762673 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320340 | ATTATAATAAAAGCT[A/G]TTTTTATCAGAAATA | 51433 |
rs750493630 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323960 | GCTAGAATTACATGG[A/G]AAGAGCAAAGGAGAA | 51433 |
rs750595340 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328849 | ATGGGCATCAAACCT[A/G]TCATAAAGAATTATC | 51433 |
rs750743988 | snp | C/T | 1.68895e-05 | 0.00290593 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318370 | CAGGAGCATGGGCAG[C/T]GCGATGGTAGGGGAG | 51433 |
rs750766324 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310898 | GAGATCACACCACTG[C/T]ACTCCAGCCTGGGTG | 51433 |
rs750776505 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311258 | GAGTGAGACCCTGTC[C/T]CTAAAAAAATAAAAT | 51433 |
rs750818130 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309587 | TAATATATATTTGTG[A/G]ACACTCAGAACTTAA | 51433 |
rs750840389 | in-del | -/CTGA | 1.64798e-05 | 0.00287047 | frameshift-variant | ANAPC5 | GRCh38.p7 | 12:121320394 | GATTACCTGGGCGTG[-/CTGA]CTATTAGGCGGAAAT | 51433 |
rs750844320 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314868 | ACTCCTGGCCTTAAG[G/T]AATCTGCCTTGGCCT | 51433 |
rs751044046 | snp | A/C/T | 3.48203e-05 | 0.00417243 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309909 | ACCCAAACCCACTGC[A/C/T]CTTCACCAGGAAGCG | 51433 |
rs751140330 | snp | A/T | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307957 | AAAAATTATGAAAAA[A/T]TCTTTTCCTTCTTAA | 51433 |
rs751254021 | snp | C/T | 4.9489e-05 | 0.00497414 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320368 | ATAAATCTATTGCCA[C/T]GCAAAAGGCAGATTA | 51433 |
rs751338806 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341457 | CCTGGGCAATGCTCT[A/G]GCCTGGGCAACAGAG | 51433 |
rs751374235 | snp | C/T | 4.94368e-05 | 0.00497152 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308546 | CTGCCGGAAGAGCAT[C/T]GCACACCGGTTCCTC | 51433 |
rs751428382 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343040 | CTTCAATTTTCACGA[C/T]GAAATTCAGTTTACT | 51433 |
rs751761912 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312974 | TTTATAACTGTAAAG[A/G]CCTACATTACAAAAG | 51433 |
rs751849813 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311390 | AGTTTAAGTTAAAAA[C/G]CGTTACAAGAGACAA | 51433 |
rs751854391 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318560 | CAATTTTTGTAAAAG[C/T]TTATGTGCCTCTGAC | 51433 |
rs751883701 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323950 | TATAAGATGAGCTAG[-/A]ATTACATGGAAAGAG | 51433 |
rs751944925 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336555 | ATTGTGGCGTGTGCC[C/T]GTACTCCCAGCTACT | 51433 |
rs752015384 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310206 | TCAAAAGAATAAAGC[A/G]AAAGAAACAAGAGAT | 51433 |
rs752142215 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342994 | AAAGAATTATAATCA[A/T]TAGTTAGATTTAAAT | 51433 |
rs752220361 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315632 | AAACCTATATATCTA[C/T]GATCAGTTGTTTTCT | 51433 |
rs752243141 | snp | C/T | 4.94393e-05 | 0.00497164 | missense | ANAPC5 | GRCh38.p7 | 12:121320390 | GGCAGATTACCTGGG[C/T]GTGCTGACTATTAGG | 51433 |
rs752244313 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318217 | CAATACTCAAACGTA[A/G]TCACAGACTCACCAG | 51433 |
rs752251968 | in-del | -/GAA | 1.68318e-05 | 0.00290096 | cds-indel | ANAPC5 | GRCh38.p7 | 12:121318386 | GCGATGGTAGGGGAG[-/GAA]GATCGCCAGTACAGC | 51433 |
rs752380094 | snp | C/G | 3.32889e-05 | 0.00407963 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320487 | CACACAATTTGATCA[C/G]CATAACCTGTGTTGA | 51433 |
rs752555885 | snp | C/T | 1.65392e-05 | 0.00287564 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308736 | TTTAACTCAACCCTT[C/T]ACGTATAGTTTTCAA | 51433 |
rs752729072 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341129 | GATTATGCCACTGCA[C/T]TCCAGCCTCAGTGAC | 51433 |
rs752761308 | snp | C/T | 1.64814e-05 | 0.00287061 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318584 | CTCTGACATTTGGTT[C/T]TGAGCTTGTAATACA | 51433 |
rs752761992 | snp | C/T | 3.3211e-05 | 0.00407485 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318461 | CAGGATGAGAAGATC[C/T]ACCACCACATCTCCG | 51433 |
rs752928275 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347357 | TTTTTCAGCCAGGTG[A/C]GGTTGCTCACACTTG | 51433 |
rs753027975 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322217 | AGGCTGGAGTGCAGT[G/T]GTGTGGTCTAGGCTC | 51433 |
rs753277943 | snp | C/T | 3.29783e-05 | 0.00406055 | missense | ANAPC5 | GRCh38.p7 | 12:121309767 | TGGCCACTAAGAACA[C/T]GGCACGACCTTTGTC | 51433 |
rs753278361 | snp | G/T | 1.66726e-05 | 0.00288722 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320497 | GATCAGCATAACCTG[G/T]GTTGAATCCACACCT | 51433 |
rs753366120 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341044 | CATCCATAAGAAATG[-/T]TTGGGCTGGGCGTGG | 51433 |
rs753376934 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339531 | GCTGAAGTACAGTGG[C/T]GAAATCTTGGCTCAC | 51433 |
rs753566399 | snp | A/G | 1.65094e-05 | 0.00287305 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121309726 | CTTCGGCTGATCGTA[A/G]GAAGCTGCTGAAGCC | 51433 |
rs753585964 | in-del | -/A | 0.000608964 | 0.0174388 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319826 | TCCATAACTAGTAAG[-/A]AAAAAAAAACACAAT | 51433 |
rs753914734 | snp | A/G | 1.71873e-05 | 0.00293144 | missense | ANAPC5 | GRCh38.p7 | 12:121319712 | CTATAAACACCCTCT[A/G]TGCTATTGAGAGCTG | 51433 |
rs753986939 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314610 | CCCCTACAGGAACAA[A/G]ATAAGGACATACACT | 51433 |
rs754133481 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343359 | AACATTTCTAGGCAC[A/C]GTTCTGAATACTTTA | 51433 |
rs754213641 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323777 | AATTACATAGAATTA[C/G]AATAAAAGATCATTA | 51433 |
rs754328081 | snp | C/T | 1.70211e-05 | 0.00291724 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318346 | CTCCTTGGAGAGGGC[C/T]AGAGCCTGCAGGAGC | 51433 |
rs754365867 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309018 | GCCAGGTGTGGTGGC[A/G]GGCACCTGTAATCCC | 51433 |
rs754440105 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315356 | GCATTAAGATGGCAA[C/T]GTTCTCCAAACTGAC | 51433 |
rs754520051 | snp | C/T | 1.66952e-05 | 0.00288917 | missense | ANAPC5 | GRCh38.p7 | 12:121319776 | ATTTGCCATCATTCA[C/T]TGCTCTGTCAAACTG | 51433 |
rs754547944 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341094 | CAGCACTTCGGGAGG[C/T]AGAGGTGTCGGTGAG | 51433 |
rs754571091 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317608 | GAAGGTAGTAAGAAA[C/G]AGATTCCTTAGCTCC | 51433 |
rs754606383 | in-del | -/ACACAA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319108 | GAGCATGCTGTGTAT[-/ACACAA]ACACAAACACACACA | 51433 |
rs754683193 | snp | C/G | 1.64866e-05 | 0.00287106 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320375 | TATTGCCATGCAAAA[C/G]GCAGATTACCTGGGC | 51433 |
rs754820567 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | ANAPC5 | GRCh38.p7 | 12:121308608 | TGGCCTGGAAGTAAA[C/T]GACGTCCCTGATGCG | 51433 |
rs755023680 | snp | C/G/T | 5.05798e-05 | 0.0050287 | missense | ANAPC5 | GRCh38.p7 | 12:121318375 | GCATGGGCAGCGCGA[C/G/T]GGTAGGGGAGGAAGA | 51433 |
rs755046944 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311416 | GACAAGGAAAAAGGA[A/G]GACATTATATACTCA | 51433 |
rs755136794 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309989 | TACCTGACATGTACT[A/G]CGTTAAAACAGGAAC | 51433 |
rs755152936 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343456 | AGAGCTCAAAGCACA[A/G]AAAGGGTGAATAACT | 51433 |
rs755346684 | snp | A/C | | | missense | ANAPC5 | GRCh38.p7 | 12:121327138 | GCAGAGTGCGACAGC[A/C]AAGGACTCTGTGTTG | 51433 |
rs755448595 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329573 | GGTCTAGTTTTCAAT[-/G]GGGTGTTTCTGAGAG | 51433 |
rs755464812 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322086 | GGTCAGGCTGCTCTC[A/G]ATCTCATGACCTCGT | 51433 |
rs755697391 | snp | C/T | 1.66471e-05 | 0.00288501 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320490 | ACAATTTGATCAGCA[C/T]AACCTGTGTTGAATC | 51433 |
rs755699638 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | ANAPC5 | GRCh38.p7 | 12:121308553 | AAGAGCATCGCACAC[C/G]GGTTCCTCTCCTGGG | 51433 |
rs755711201 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317708 | GCAATAATTCTAATG[C/T]ACAGCCAGTTTGGAG | 51433 |
rs755711423 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337126 | GGGAGGCTGAGGCAG[A/G]AGAATCACTTGAACC | 51433 |
rs755783623 | snp | A/G | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307930 | CTGAAAAATGCTCCT[A/G]GTCATTGGTCCAAAA | 51433 |
rs755799297 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339311 | CTGCCTCTGCCTCCC[A/C]AAGTGCTGGGATTAT | 51433 |
rs755826246 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308630 | CCTGATGCGCTCTTT[A/G]CAGTCAACCTTTGCA | 51433 |
rs755877321 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311371 | TGAGTATCATACAAT[A/G]TAGAGTTTAAGTTAA | 51433 |
rs756060109 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311525 | TGACAGATTTGAAGG[A/G]AGAAATAGACAATTC | 51433 |
rs756062832 | snp | C/T | 1.65971e-05 | 0.00288067 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318463 | GGATGAGAAGATCCA[C/T]CACCACATCTCCGTG | 51433 |
rs756182098 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329076 | TCAAGGAGCCACTTT[C/T]GTCATTATAATCAAT | 51433 |
rs756198010 | snp | A/G | 1.64893e-05 | 0.0028713 | missense | ANAPC5 | GRCh38.p7 | 12:121318594 | TGGTTCTGAGCTTGT[A/G]ATACAACCGCTTTCC | 51433 |
rs756405312 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323675 | AATACTTTCAATTTG[A/T]CTCAATCCTTTCATG | 51433 |
rs756499501 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322245 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 51433 |
rs756603335 | snp | G/T | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307970 | AAATCTTTTCCTTCT[G/T]AATCTCCAGTCAGGG | 51433 |
rs756643861 | snp | G/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352724 | TTGTTGTTGTTGGTG[G/T]TGGTGGTGGTGGTTG | 51433 |
rs756647105 | snp | C/T | 1.64906e-05 | 0.00287142 | missense | ANAPC5 | GRCh38.p7 | 12:121309772 | ACTAAGAACATGGCA[C/T]GACCTTTGTCCAGGA | 51433 |
rs756770990 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308663 | ATAGTTCTTGGCTTC[A/G]TTGAGGTTCTCGATG | 51433 |
rs756826058 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320474 | CCTAAAGTAGAAACA[C/T]ACAATTTGATCAGCA | 51433 |
rs756979263 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313665 | GTAAAATGAACAAAT[C/T]CCTAGAAAGACCAAA | 51433 |
rs757175144 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314773 | GGGATTACAGGCATG[C/T]ACCACCACCACTACA | 51433 |
rs757303004 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350100 | CCCTGGGAGCCACAA[C/G]TTATAAAGACATCCC | 51433 |
rs757324506 | snp | A/C/G | 6.7536e-05 | 0.00581069 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121319738 | AGCTGTGATTCCTGT[A/C/G]ACAAGTGAATCAGCC | 51433 |
rs757483142 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323852 | CCGCCACAGGGAGTC[A/G]GGCATGGGGATATAG | 51433 |
rs757525910 | in-del | -/A | 0.000608964 | 0.0174388 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319827 | TCCATAACTAGTAAG[-/A]AAAAAAAACACAATT | 51433 |
rs757540245 | snp | C/T | 1.80827e-05 | 0.00300683 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318236 | CAGACTCACCAGCTC[C/T]TGAGCACAAATATGT | 51433 |
rs757698290 | in-del | -/ATA | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307887 | GCCCATGCAGAATAT[-/ATA]ATAAGAAAGCCAACA | 51433 |
rs757746927 | snp | A/G | 1.70032e-05 | 0.0029157 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318349 | CTTGGAGAGGGCCAG[A/G]GCCTGCAGGAGCATG | 51433 |
rs757811897 | snp | A/T | 1.64895e-05 | 0.00287132 | missense | ANAPC5 | GRCh38.p7 | 12:121309763 | CACTTGGCCACTAAG[A/T]ACATGGCACGACCTT | 51433 |
rs758057057 | snp | G/T | 1.65625e-05 | 0.00287766 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318640 | ATGAACACAAGTGTT[G/T]TAACTAGTCACTTTG | 51433 |
rs758188448 | snp | A/G | 1.67978e-05 | 0.00289804 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121319750 | TGTAACAAGTGAATC[A/G]GCCAAATGATATTTG | 51433 |
rs758219880 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315146 | GATATAAGATCAATA[C/T]AAACTAGCAACCCAA | 51433 |
rs758224880 | snp | C/T | 3.30229e-05 | 0.0040633 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320363 | CAGAAATAAATCTAT[C/T]GCCATGCAAAAGGCA | 51433 |
rs758299325 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341197 | GAAATGTTTGGGGCA[C/T]GCTGGTTCATGTCTG | 51433 |
rs758345264 | snp | C/T | | | utr-variant-3-prime | ANAPC5 | GRCh38.p7 | 12:121308371 | CTAATCAGAATGCTG[C/T]TTATTGACAAGATAG | 51433 |
rs758423114 | snp | A/G/T | 6.59266e-05 | 0.00574106 | synonymous-codon, missense | ANAPC5 | GRCh38.p7 | 12:121308536 | CCTGATGCAGCTGCC[A/G/T]GAAGAGCATCGCACA | 51433 |
rs758553252 | snp | A/C/T | 0.000234378 | 0.010823 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318269 | TATAAAAACAGAGAT[A/C/T]GGCTTACCTGCGCAA | 51433 |
rs758573601 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347401 | TTGCGAGGTGGAAGC[A/G]GAGGGATTGCTTGAG | 51433 |
rs758951660 | in-del | -/TTCC | 0.000115375 | 0.00759437 | frameshift-variant | ANAPC5 | GRCh38.p7 | 12:121320415 | ATTAGGCGGAAATCG[-/TTCC]TTCAAGTGCTTTAAC | 51433 |
rs758979823 | in-del | -/AAAC | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315524 | CACTTCCTGATTTCA[-/AAAC]TTACTACAAAGCTAT | 51433 |
rs759014907 | snp | C/T | 1.66891e-05 | 0.00288864 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320499 | TCAGCATAACCTGTG[C/T]TGAATCCACACCTGC | 51433 |
rs759087529 | snp | A/G | 1.72615e-05 | 0.00293776 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318328 | CAAGTACTGTAACCG[A/G]TACTCCTTGGAGAGG | 51433 |
rs759088894 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342990 | AGACAAAGAATTATA[A/T]TCATTAGTTAGATTT | 51433 |
rs759197702 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320121 | CTTTCTCTTTTTTCA[A/T]AGTAGGCACTCAATT | 51433 |
rs759281846 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325405 | GAGGCAGAGGTTGCA[A/G]TGAGCTGAGATCACA | 51433 |
rs759297605 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344635 | GATAGGCGCTACCTC[A/G]TGGTCAGGGAGGCCC | 51433 |
rs759409223 | snp | C/T | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355836 | GCACTCTAGCCTGGA[C/T]GACAGAGTGAGACTC | 51433 |
rs759495375 | snp | C/T | | | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121328378 | ATCGATGAGCTCTGA[C/T]AGGCTGTGTTTCCAG | 51433 |
rs759528624 | in-del | -/T | 1.66283e-05 | 0.00288338 | frameshift-variant | ANAPC5 | GRCh38.p7 | 12:121309702 | GTACAGCTTCCTACC[-/T]TCTGCTTTCTTCGGC | 51433 |
rs759938956 | snp | G/T | 1.85858e-05 | 0.00304837 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319679 | TATTCTGGGGTTAGA[G/T]TTTTCAAGGTTTCTT | 51433 |
rs760044471 | snp | C/T | 1.70945e-05 | 0.00292351 | utr-variant-3-prime | ANAPC5 | GRCh38.p7 | 12:121308448 | GTCCAAAATCTTATA[C/T]TCTGCACAGCAGCCC | 51433 |
rs760093850 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332523 | ATCTGAGATATTACA[A/C]CTATGCTTAGCGTTG | 51433 |
rs760321498 | in-del | -/ATATTTATTGAAAG | 1.66646e-05 | 0.00288652 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318445 | GTAAAGAGGAAAACA[-/ATATTTATTGAAAG]CAGGATGAGAAGATC | 51433 |
rs760391084 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320246 | TTATATAAATAATAT[C/T]ATACTTGTAAGCATC | 51433 |
rs760436803 | snp | C/G/T | 3.30935e-05 | 0.00406766 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308738 | TAACTCAACCCTTCA[C/G/T]GTATAGTTTTCAAAA | 51433 |
rs760464502 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340723 | ACACCCGGCTAATTT[G/T]TGTGTGTGTGTTTTT | 51433 |
rs760561463 | snp | C/T | 0.000115633 | 0.00760283 | missense | ANAPC5 | GRCh38.p7 | 12:121309722 | CTTTCTTCGGCTGAT[C/T]GTAGGAAGCTGCTGA | 51433 |
rs760573423 | in-del | GAGACAGAGTCTTGCTCTGTCACCCAGGCT/TGAGAAGGG | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321550 | TTTTTTTTTTTTTTT[lengthTooLong]GGAGTGCAGTGGCAT | 51433 |
rs760587461 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321812 | TCAAGTGCTGGGATT[A/G]CAGGCATGAGCCAAT | 51433 |
rs760639854 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351305 | CTGAGCCTGAGAGGT[C/T]GAGGCTGCAGTGAGC | 51433 |
rs760768723 | snp | A/G | 1.73724e-05 | 0.00294719 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121319705 | TTCTTACCTATAAAC[A/G]CCCTCTATGCTATTG | 51433 |
rs760968138 | snp | A/G | 1.67483e-05 | 0.00289377 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319837 | GTAAGAAAAAAAAAC[A/G]CAATTAAGTACAAAA | 51433 |
rs761125530 | in-del | -/TCATT | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342980 | ATTTCTTTTAGACAA[-/TCATT]AGAATTATAATCATT | 51433 |
rs761340650 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322117 | GATCCGCCTGCCTCG[G/T]TCTCCCAAAGTGCTG | 51433 |
rs761505104 | snp | G/T | 3.35756e-05 | 0.00409716 | splice-acceptor-variant | ANAPC5 | GRCh38.p7 | 12:121309865 | ATTCCAAGAATGAGC[G/T]GAAAAAGAAACATCA | 51433 |
rs761518817 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323047 | AAAACAAACAAACAA[A/G]CAAAAAACCTTAGAA | 51433 |
rs761710625 | snp | A/C/G | 4.94273e-05 | 0.00497108 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345899 | TCATCTCTACTGGTC[A/C/G]GTTCCATATCAGCAT | 51433 |
rs761831127 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318102 | AAGTGTCAGTTTGTC[A/T]CCAGGTTCACACCTC | 51433 |
rs762075756 | snp | C/T | 1.64988e-05 | 0.00287213 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121320445 | TAACACTTCAGAAGC[C/T]GCAGCAAAACAGCCC | 51433 |
rs762080042 | snp | A/G | 1.64863e-05 | 0.00287104 | missense | ANAPC5 | GRCh38.p7 | 12:121308527 | AGGGCAGCTCCTGAT[A/G]CAGCTGCCGGAAGAG | 51433 |
rs762129065 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | ANAPC5 | GRCh38.p7 | 12:121308589 | CCCAGGGTATGGTAG[A/G]GTCTGGCCTGGAAGT | 51433 |
rs762188435 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328772 | TGCCTCTGCTACTTA[A/C]TGTGTGACTTAGGGC | 51433 |
rs762193964 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316505 | TTGGGAGGCCGAGGT[-/G]GGCGGATCACGAGGT | 51433 |
rs762208161 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340279 | GCTGAGATCACCACC[A/G]CACTCCAGCCTGGGC | 51433 |
rs762243013 | snp | A/C/T | 5.01847e-05 | 0.00500902 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318430 | CAGTAGGACACTGAC[A/C/T]GTAAAGAGGAAAACA | 51433 |
rs762263274 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314093 | TTCAATACACAAATA[C/T]ATAAATAAAATGAAA | 51433 |
rs762272745 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338766 | AGTCTTTGTTCTGTA[C/T]GTGTGTATATATGTT | 51433 |
rs762318552 | snp | A/C | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307900 | TATATAAGAAAGCCA[A/C]CATCTAGAAAGGGAC | 51433 |
rs762378903 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310805 | TGGGCATAGTGGCAC[A/G]CACCTGTAATCTCAG | 51433 |
rs762452705 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345363 | CACATTCAAATTGAG[C/T]AGTCTGAGAAGAGTT | 51433 |
rs762459423 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320621 | TTCTTTTTTTTTTTT[-/G]GGGACAGAGTCTCGC | 51433 |
rs762616178 | snp | G/T | 1.70278e-05 | 0.00291781 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309887 | GAAACATCATGGCAC[G/T]GTACATACCCAAACC | 51433 |
rs762738459 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321763 | GGCTGGTCTCAAACT[C/T]CTGGCCTCAAGCAAT | 51433 |
rs762932825 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342997 | GAATTATAATCATTA[G/T]TTAGATTTAAATATA | 51433 |
rs762959937 | snp | A/C | 3.30972e-05 | 0.00406786 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320467 | AAACAGCCCTAAAGT[A/C]GAAACACACAATTTG | 51433 |
rs763115890 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308600 | GTAGAGTCTGGCCTG[A/G]AAGTAAACGACGTCC | 51433 |
rs763269606 | snp | A/T | 3.34018e-05 | 0.00408654 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318433 | TAGGACACTGACCGT[A/T]AAGAGGAAAACACAG | 51433 |
rs763278262 | in-del | -/ACACAA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319109 | GAGCATGCTGTGTAT[-/ACACAA]ACACACACACACACA | 51433 |
rs763397997 | snp | A/G | 6.59152e-05 | 0.00574049 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318518 | GATCACCATTTCTGT[A/G]TTCTTCAGTTTCTGA | 51433 |
rs763555150 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314049 | ATACACTATGACCAT[A/G]TGAAATTTACTCCAG | 51433 |
rs763801949 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321818 | GCTGGGATTACAGGC[A/C]TGAGCCAATGTGCCC | 51433 |
rs763816672 | in-del | -/CTTCTATGTGTAGGGCCTATAAGGTACTAGGGAATAT | 1.66707e-05 | 0.00288705 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318446 | TAAAGAGGAAAACAC[lengthTooLong]AGGATGAGAAGATCC | 51433 |
rs763890124 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320350 | AAGCTATTTTTATCA[A/G]AAATAAATCTATTGC | 51433 |
rs763895505 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317254 | TCTTGTGTTACATAC[-/T]TTTTTTTTTTTTTTT | 51433 |
rs763911589 | snp | A/G | 3.30327e-05 | 0.0040639 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121309723 | TTTCTTCGGCTGATC[A/G]TAGGAAGCTGCTGAA | 51433 |
rs764030245 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343038 | TTCTTCAATTTTCAC[A/G]ATGAAATTCAGTTTA | 51433 |
rs764085218 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314573 | TAGCATGATATTTGA[A/T]GATGAAAGACTGAAC | 51433 |
rs764122952 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309520 | ATTCACTTGTCCTCA[A/G]TCTTTCTGCCAAGCA | 51433 |
rs764263632 | snp | C/T | 1.64868e-05 | 0.00287109 | missense | ANAPC5 | GRCh38.p7 | 12:121308523 | TGAGAGGGCAGCTCC[C/T]GATGCAGCTGCCGGA | 51433 |
rs764274698 | snp | A/C | 1.72892e-05 | 0.00294012 | missense | ANAPC5 | GRCh38.p7 | 12:121319708 | TTACCTATAAACACC[A/C]TCTATGCTATTGAGA | 51433 |
rs764401591 | snp | G/T | 6.70365e-05 | 0.00578911 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319845 | AAAAAACACAATTAA[G/T]TACAAAATGGCGAAT | 51433 |
rs764548180 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308914 | AGCACTTTGGGAGGC[C/G]GAGGCGGGTGGATCA | 51433 |
rs764695537 | snp | A/C | 1.75591e-05 | 0.00296298 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309915 | ACCCACTGCCCTTCA[A/C]CAGGAAGCGTTTCAT | 51433 |
rs764730693 | in-del | -/AA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319114 | TGCTGTGTATACACA[-/AA]CACACACACACACAC | 51433 |
rs764748647 | snp | A/G | 1.71073e-05 | 0.00292461 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318337 | TAACCGGTACTCCTT[A/G]GAGAGGGCCAGAGCC | 51433 |
rs764780162 | snp | C/T | 1.64904e-05 | 0.00287139 | missense | ANAPC5 | GRCh38.p7 | 12:121309745 | GCTGCTGAAGCCACC[C/T]GGCACTTGGCCACTA | 51433 |
rs764841654 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342992 | ACAAAGAATTATAAT[C/T]ATTAGTTAGATTTAA | 51433 |
rs764973867 | in-del | -/CT | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310761 | CAACATGGTGAAACC[-/CT]GTCTTTCCTAAAAAT | 51433 |
rs765059617 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325569 | TTCTATTCTAATAGT[-/A]AAAAAAAAATAATTT | 51433 |
rs765117433 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316456 | CAGGTATTCAACCCC[A/G]GGCGCGGTGGCTCAC | 51433 |
rs765209386 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314917 | CAGGTGTGAGACACC[A/G]AGCCAAGACACACAC | 51433 |
rs765322544 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321344 | GAACAAACAAATTAC[-/T]TTTTTTTTTTTTTTT | 51433 |
rs765497377 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ANAPC5 | GRCh38.p7 | 12:121308596 | TATGGTAGAGTCTGG[C/T]CTGGAAGTAAACGAC | 51433 |
rs765527619 | snp | C/T | 1.69089e-05 | 0.0029076 | missense | ANAPC5 | GRCh38.p7 | 12:121318363 | GAGCCTGCAGGAGCA[C/T]GGGCAGCGCGATGGT | 51433 |
rs765720405 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311152 | GTAGTCCTAGCTACT[C/T]GGGAGACTGAGTTGG | 51433 |
rs765924596 | snp | C/T | | | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307903 | ATAAGAAAGCCAACA[C/T]CTAGAAAGGGACTGA | 51433 |
rs766069397 | snp | C/T | 1.74275e-05 | 0.00295186 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318319 | TTCAGAGGCCAAGTA[C/T]TGTAACCGGTACTCC | 51433 |
rs766197602 | snp | A/G | 4.94907e-05 | 0.00497422 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320367 | AATAAATCTATTGCC[A/G]TGCAAAAGGCAGATT | 51433 |
rs766204754 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325216 | GCCTATAATCCCAAC[A/G]CTCTGGGAGGCCAAG | 51433 |
rs766212969 | snp | A/G | 1.65611e-05 | 0.00287755 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320471 | AGCCCTAAAGTAGAA[A/G]CACACAATTTGATCA | 51433 |
rs766393925 | snp | A/T | | | missense | ANAPC5 | GRCh38.p7 | 12:121318283 | TCGGCTTACCTGCGC[A/T]AAAGCCAAGTTCAGC | 51433 |
rs766633868 | snp | A/T | 6.6778e-05 | 0.00577793 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318435 | GGACACTGACCGTAA[A/T]GAGGAAAACACAGGA | 51433 |
rs766668155 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311297 | AAATCAGCTGAAAGT[A/G]AAAGGATAGAAAAAT | 51433 |
rs766760644 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | ANAPC5 | GRCh38.p7 | 12:121318537 | TTCAGTTTCTGACAA[C/T]GAACCAACAATTTTT | 51433 |
rs766782437 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315005 | AAAAGAAATACAGGG[C/T]ATCTAAGTGGGAATG | 51433 |
rs766859328 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312939 | AACTACAAATTTATG[A/G]AATATAGTTCTCAAG | 51433 |
rs766870329 | in-del | -/T | 1.6489e-05 | 0.00287128 | frameshift-variant | ANAPC5 | GRCh38.p7 | 12:121309751 | GAAGCCACCTGGCAC[-/T]TGGCCACTAAGAACA | 51433 |
rs766908291 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317279 | TTTTTTTGAGATGGA[A/G]TCTCGCTCTGTTGCC | 51433 |
rs766944732 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322309 | GATTACAGGCAGACA[C/T]CACCACACCCAGCTA | 51433 |
rs767028290 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310715 | CAGGCGGGCAGATCA[C/G]TTGAGGTCAGGGGTT | 51433 |
rs767253099 | snp | A/C | 1.66167e-05 | 0.00288237 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320483 | GAAACACACAATTTG[A/C]TCAGCATAACCTGTG | 51433 |
rs767344712 | snp | A/C | 1.65184e-05 | 0.00287384 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308731 | ACACATTTAACTCAA[A/C]CCTTCACGTATAGTT | 51433 |
rs767682233 | snp | G/T | 1.81092e-05 | 0.00300903 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319688 | GTTAGAGTTTTCAAG[G/T]TTTCTTACCTATAAA | 51433 |
rs767742591 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314447 | CATATGATCAAATCA[A/G]TCAATGCAGAAAAAA | 51433 |
rs767869691 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328812 | AGCTTCTTAGCTAAG[A/C]CTCAGCTTCCTCATC | 51433 |
rs767947385 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338787 | TATATATGTTACATA[C/T]CATATTCTGATTTTG | 51433 |
rs768043829 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314599 | GAACGCTTTCCCCCT[-/A]ACAGGAACAAAATAA | 51433 |
rs768061017 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322200 | GTCTCACTGTGTCAC[C/G]CAGGCTGGAGTGCAG | 51433 |
rs768072998 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313928 | ATACTAAAGCCAAAG[A/G]AAGATATCACAAGAA | 51433 |
rs768230016 | snp | A/G | 1.66352e-05 | 0.00288398 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318658 | ACTAGTCACTTTGAG[A/G]GTAAGAATCTCAATT | 51433 |
rs768508138 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322938 | GCAAAGGCAGGAGAA[C/T]CGCTTGAACCCAGGA | 51433 |
rs768519725 | snp | A/G | 1.65858e-05 | 0.00287969 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121309837 | GTGGAGAAGACTTAA[A/G]GCCTGTTCTGGGATT | 51433 |
rs768644285 | snp | C/T | 3.59299e-05 | 0.00423835 | missense | ANAPC5 | GRCh38.p7 | 12:121318278 | AGAGATCGGCTTACC[C/T]GCGCAAAAGCCAAGT | 51433 |
rs768731169 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318017 | ATCATTAATATGATG[A/C]AGGTGTTCTCACTGA | 51433 |
rs768832165 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316577 | CTCTACTAAAAATAC[-/A]AAAAAAATAGCTGGG | 51433 |
rs768934998 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321343 | GAACAAACAAATTAC[-/T]TTTTTTTTTTTTTTT | 51433 |
rs768976217 | snp | C/T | 1.648e-05 | 0.0028705 | missense | ANAPC5 | GRCh38.p7 | 12:121308674 | CTTCATTGAGGTTCT[C/T]GATGGCAGCCTCCAG | 51433 |
rs769042466 | snp | C/T | 6.59598e-05 | 0.00574243 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121320430 | TTCCTTCAAGTGCTT[C/T]AACACTTCAGAAGCT | 51433 |
rs769315875 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345199 | TGCATTTTGGGCTTG[A/T]CCAACTAAGTGAGTA | 51433 |
rs769405526 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310446 | CACATGCCTGCAGTC[C/T]CAGTTACTCAGGAGG | 51433 |
rs769682963 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314401 | GGGCAACAGAGTGAC[-/A]CTCTATCTCAAAAAC | 51433 |
rs769703741 | snp | A/G | 3.36559e-05 | 0.00410205 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318388 | GATGGTAGGGGAGGA[A/G]GATCGCCAGTACAGC | 51433 |
rs769875337 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318107 | TCAGTTTGTCACCAG[C/G]TTCACACCTCCACAG | 51433 |
rs769974664 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308884 | CTGGGCGAAGTGGCT[C/T]ATGCCTGTAATCCTA | 51433 |
rs770020825 | snp | A/C/G | 4.9594e-05 | 0.00497945 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320462 | CAGCAAAACAGCCCT[A/C/G]AAGTAGAAACACACA | 51433 |
rs770065122 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319400 | ACCATGCCTGGCTAA[A/T]TTTTTGTACTTTTAG | 51433 |
rs770207933 | snp | A/C/T | 4.94705e-05 | 0.00497325 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308696 | AGCCTCCAGAGCTGA[A/C/T]GGAAAGGGGAAAATA | 51433 |
rs770260822 | snp | A/G | 1.69143e-05 | 0.00290807 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309667 | AATGCTTTCTGGAAT[A/G]GCATTGCCTAACAGT | 51433 |
rs770303493 | snp | C/G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312518 | GAGACCATCCTAACA[C/G/T]GATGAAACCCCAGCT | 51433 |
rs770543653 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310515 | TTGCAGTGAGCCACA[A/G]TCGTGCCACTGCACT | 51433 |
rs770749369 | snp | C/G | 1.67947e-05 | 0.00289777 | missense | ANAPC5 | GRCh38.p7 | 12:121318408 | GCCAGTACAGCTCTG[C/G]CACGGACAGTAGGAC | 51433 |
rs770872119 | snp | A/G | 1.65392e-05 | 0.00287564 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318478 | CCACCACATCTCCGT[A/G]AGATGTACAAGAGAC | 51433 |
rs770976555 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354753 | CCTCACTCTATTAAT[A/G]AAAAAGCATACTTAC | 51433 |
rs771061941 | snp | A/C | 4.94768e-05 | 0.00497352 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308699 | CTCCAGAGCTGACGG[A/C]AAGGGGAAAATAACA | 51433 |
rs771383232 | in-del | -/AA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342983 | TTCTTTTAGACAAAG[-/AA]TTATAATCATTAGTT | 51433 |
rs771534246 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319481 | TCAAGTGATGCGCCC[A/G]CCTCAGCCTCCCAAA | 51433 |
rs771572792 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350975 | ATTTACTACATGCTA[A/G]TAACAGTTTCTACTA | 51433 |
rs771626968 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324844 | CTATGATTGTGCCAC[C/T]GCACTCCATCCTGGG | 51433 |
rs771681855 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327580 | GCACAGACTGCTCTG[C/G]CAATGTAAGCAGTGG | 51433 |
rs771701266 | snp | C/G | 6.60775e-05 | 0.00574755 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318486 | TCTCCGTGAGATGTA[C/G]AAGAGACCCCTTACC | 51433 |
rs771821427 | in-del | -/AAAAAAAAAAAAAAAAAA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316733 | GCGAGACTCTGTCTC[-/AAAAAAAAAAAAAAAAAA]AAAAAAAGAAAACAG | 51433 |
rs772003492 | in-del | -/TC | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316725 | GTGACAGAGCGAGAC[-/TC]TGTCTCAAAAAAAAA | 51433 |
rs772042736 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311982 | GGCCCTAACATATAT[A/G]TATAAAGCATGCCAC | 51433 |
rs772164665 | snp | A/G | 1.65184e-05 | 0.00287384 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121309813 | AGCCAAGATGGGCTC[A/G]ATGGCCATGTGGAGA | 51433 |
rs772194550 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321728 | TTTTTAGTAGAGGCA[A/G]TGTTTTGCCATGTTG | 51433 |
rs772204556 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318945 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGATTGC | 51433 |
rs772401735 | snp | C/T | 3.29603e-05 | 0.00405944 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121320406 | GTGCTGACTATTAGG[C/T]GGAAATCGTTCCTTC | 51433 |
rs772514778 | snp | A/G | 5.01358e-05 | 0.00500653 | utr-variant-3-prime | ANAPC5 | GRCh38.p7 | 12:121308464 | TCTGCACAGCAGCCC[A/G]GCAGGGATGTCCTCT | 51433 |
rs772518488 | snp | A/G | 6.67456e-05 | 0.00577654 | missense | ANAPC5 | GRCh38.p7 | 12:121319815 | GATCACATAGCATCC[A/G]TAACTAGTAAGAAAA | 51433 |
rs772633714 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | ANAPC5 | GRCh38.p7 | 12:121308563 | CACACCGGTTCCTCT[C/T]CTGGGTCTTCCCCAG | 51433 |
rs772672165 | snp | A/G | 1.71808e-05 | 0.00293089 | utr-variant-3-prime | ANAPC5 | GRCh38.p7 | 12:121308438 | ACATGAACAAGTCCA[A/G]AATCTTATACTCTGC | 51433 |
rs772702699 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317859 | AATGAAGAGTCAATT[C/T]CTTCATGGCCTTTAC | 51433 |
rs772717788 | snp | C/T | 3.38324e-05 | 0.00411279 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309878 | GCTGAAAAAGAAACA[C/T]CATGGCACTGTACAT | 51433 |
rs773018580 | snp | C/T | 1.78717e-05 | 0.00298923 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318289 | TACCTGCGCAAAAGC[C/T]AAGTTCAGCACTGTT | 51433 |
rs773046338 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351195 | GGGTAACATGGCAAA[A/G]TCCCGTCTCTACAAA | 51433 |
rs773264001 | snp | C/T | | | missense | ANAPC5 | GRCh38.p7 | 12:121319748 | CCTGTAACAAGTGAA[C/T]CAGCCAAATGATATT | 51433 |
rs773331253 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332034 | ATAGATATAGAGTCT[C/T]ACTATGTTCCCCAGG | 51433 |
rs773483741 | snp | A/G | 1.64735e-05 | 0.00286993 | stop-gained | ANAPC5 | GRCh38.p7 | 12:121308599 | GGTAGAGTCTGGCCT[A/G]GAAGTAAACGACGTC | 51433 |
rs773683519 | snp | A/G | 3.2969e-05 | 0.00405998 | missense | ANAPC5 | GRCh38.p7 | 12:121318510 | CCTTACCTGATCACC[A/G]TTTCTGTGTTCTTCA | 51433 |
rs773705912 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314030 | ATAGCACGTTAAAAG[C/G]AACATACACTATGAC | 51433 |
rs773712895 | in-del | -/TG | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323151 | TTCATACCAGAACTC[-/TG]TGCTTTTCTTCCTCT | 51433 |
rs774105993 | in-del | -/AACTC | 0.000297147 | 0.0121855 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308724 | ATAACACACACATTT[-/AACTC]AACCCTTCACGTATA | 51433 |
rs774125294 | snp | C/T | 1.67851e-05 | 0.00289694 | missense | ANAPC5 | GRCh38.p7 | 12:121318411 | AGTACAGCTCTGCCA[C/T]GGACAGTAGGACACT | 51433 |
rs774253046 | snp | C/G | 1.65012e-05 | 0.00287234 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308713 | GAAAGGGGAAAATAA[C/G]ACACACATTTAACTC | 51433 |
rs774370591 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320101 | CCTTTGCAAATTCTA[C/T]GTCTCTTTCTCTTTT | 51433 |
rs774455102 | snp | C/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355912 | GTTTCCAACTCACTA[C/G]AATCCTCATCAATCG | 51433 |
rs774549775 | snp | C/T | 8.2837e-05 | 0.00643519 | missense | ANAPC5 | GRCh38.p7 | 12:121309709 | TTCCTACCTTCTGCT[C/T]TCTTCGGCTGATCGT | 51433 |
rs774658916 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338722 | CTACCCAGAAATAAC[A/G]CTATTAATACTTTAG | 51433 |
rs774753658 | snp | A/T | 1.86225e-05 | 0.00305138 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319678 | TTATTCTGGGGTTAG[A/T]GTTTTCAAGGTTTCT | 51433 |
rs774821961 | in-del | -/CTCGGT | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322113 | TCGTGATCCGCCTGC[-/CTCGGT]CTCCCAAAGTGCTGG | 51433 |
rs774924388 | snp | C/T | 1.65045e-05 | 0.00287263 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318493 | GAGATGTACAAGAGA[C/T]CCCTTACCTGATCAC | 51433 |
rs775033093 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315678 | AACTGGTTTTTAACA[C/G]GGGTACCAAAACCAT | 51433 |
rs775050604 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312430 | TTACCCAGGTAGCCA[A/G]GCACAGCGGCTCACA | 51433 |
rs775150290 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348493 | AACATGGCAAAACCC[C/T]GTCTCTACTAAAAAC | 51433 |
rs775391321 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328697 | TCTGGGAGAGAGGCA[A/G]AGGGTACACGGGAAA | 51433 |
rs775479341 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331724 | CACTGCTGAGGGGAA[A/G]GGCAAGGAGAGGATA | 51433 |
rs775514694 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338545 | AGTGAGCCGAAATCA[C/T]GCCACTGCACTCCAG | 51433 |
rs775601289 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314452 | GATCAAATCAATCAA[C/T]GCAGAAAAAAAAAAT | 51433 |
rs775707959 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321762 | AGGCTGGTCTCAAAC[C/T]CCTGGCCTCAAGCAA | 51433 |
rs775715410 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315859 | TGTGAGAAGAAAACA[C/T]AGAAGAAAATCTTCA | 51433 |
rs776008927 | in-del | -/CACA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319110 | AGCATGCTGTGTATA[-/CACA]AACACACACACACAC | 51433 |
rs776034517 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308582 | GGTCTTCCCCAGGGT[A/G]TGGTAGAGTCTGGCC | 51433 |
rs776074808 | snp | A/G | 1.66421e-05 | 0.00288458 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318659 | CTAGTCACTTTGAGG[A/G]TAAGAATCTCAATTT | 51433 |
rs776368766 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342988 | TTAGACAAAGAATTA[G/T]AATCATTAGTTAGAT | 51433 |
rs776463402 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328096 | ACCCACCCATTACCT[C/T]ACAAAGTGGTTGGGA | 51433 |
rs776465097 | snp | G/T | 1.67728e-05 | 0.00289588 | missense | ANAPC5 | GRCh38.p7 | 12:121309863 | GGATTCCAAGAATGA[G/T]CTGAAAAAGAAACAT | 51433 |
rs776562329 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351831 | TTATCCCTGTGTCTC[C/T]AACGCTCTATTGTAT | 51433 |
rs776672836 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316448 | AATGAAAACAGGTAT[C/T]CAACCCCGGGCGCGG | 51433 |
rs776818762 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | ANAPC5 | GRCh38.p7 | 12:121308586 | TTCCCCAGGGTATGG[C/T]AGAGTCTGGCCTGGA | 51433 |
rs776867768 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318063 | TTACTGAATACACAG[C/G]TCAGGAAAGCCAGTG | 51433 |
rs776869707 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338432 | GTCTCTACTAAAGAT[-/A]CAAAACATTAGCCGG | 51433 |
rs776891787 | snp | C/T | 1.64866e-05 | 0.00287106 | missense | ANAPC5 | GRCh38.p7 | 12:121308526 | GAGGGCAGCTCCTGA[C/T]GCAGCTGCCGGAAGA | 51433 |
rs776920025 | snp | G/T | 5.03563e-05 | 0.00501753 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319853 | CAATTAAGTACAAAA[G/T]GGCGAATGTTCATCT | 51433 |
rs776967113 | snp | A/G | 1.6498e-05 | 0.00287206 | missense | ANAPC5 | GRCh38.p7 | 12:121320441 | GCTTTAACACTTCAG[A/G]AGCTGCAGCAAAACA | 51433 |
rs777227752 | in-del | -/AA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310933 | GTGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 51433 |
rs777243352 | in-del | -/ACAGA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316009 | GTGAAAAGACCAAAC[-/ACAGA]ACAGGAGAAAATATT | 51433 |
rs777357193 | snp | C/G | 1.66663e-05 | 0.00288667 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320494 | TTTGATCAGCATAAC[C/G]TGTGTTGAATCCACA | 51433 |
rs777440266 | snp | A/G | 3.36559e-05 | 0.00410205 | stop-gained | ANAPC5 | GRCh38.p7 | 12:121318393 | TAGGGGAGGAAGATC[A/G]CCAGTACAGCTCTGC | 51433 |
rs777647231 | in-del | -/TTAT | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319576 | CTTACCTGTATTTTC[-/TTAT]TTATTAAGAAAATAA | 51433 |
rs777720664 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313257 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGAGAG | 51433 |
rs777736756 | snp | C/T | 3.31148e-05 | 0.00406894 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318475 | CCACCACCACATCTC[C/T]GTGAGATGTACAAGA | 51433 |
rs777801922 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322322 | CACCACCACACCCAG[A/C]TAGTTTTTGTATTTT | 51433 |
rs777976701 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347567 | GCTCAGGAAGTCCAG[A/G]CTGCGTTGAGCCCTG | 51433 |
rs778040795 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321109 | ACAAAATTAGCTGGG[C/T]GTGGTGGCTCATGCC | 51433 |
rs778148851 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333201 | TGCACCTGTAGTCCC[A/G]GCTACTCGGGAAGCT | 51433 |
rs778163858 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322688 | GAATATCTTGGTGCA[A/T]AGAGCTTTGCATACT | 51433 |
rs778238400 | snp | C/T | 9.88663e-05 | 0.00703018 | missense | ANAPC5 | GRCh38.p7 | 12:121308664 | TAGTTCTTGGCTTCA[C/T]TGAGGTTCTCGATGG | 51433 |
rs778284423 | snp | A/G | 4.94719e-05 | 0.00497328 | missense | ANAPC5 | GRCh38.p7 | 12:121309773 | CTAAGAACATGGCAC[A/G]ACCTTTGTCCAGGAT | 51433 |
rs778480873 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312043 | CAAGTGCATATGGAA[C/T]ACTTTCCAGGATAGA | 51433 |
rs778488075 | snp | A/G/T | 4.97231e-05 | 0.00498593 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308743 | CAACCCTTCACGTAT[A/G/T]GTTTTCAAAACGTGG | 51433 |
rs778677144 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313723 | AATCTGAATAGACCT[A/G]TAACAACTAAAGAGA | 51433 |
rs778679044 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316732 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51433 |
rs778811549 | snp | C/T | 1.65272e-05 | 0.0028746 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318482 | CACATCTCCGTGAGA[C/T]GTACAAGAGACCCCT | 51433 |
rs778868797 | snp | C/T | 1.65176e-05 | 0.00287376 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318615 | ACCGCTTTCCTGAAA[C/T]AGAATCAAAATGAAC | 51433 |
rs779233762 | snp | C/T | 1.65384e-05 | 0.00287557 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121327177 | CACGCCCGCATTCAC[C/T]GCCTCCAGGCTGTTC | 51433 |
rs779361901 | in-del | -/AATT | 5.02449e-05 | 0.00501198 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319839 | AAGAAAAAAAAACAC[-/AATT]AAGTACAAAATGGCG | 51433 |
rs779654373 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320997 | GCTAACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 51433 |
rs779660525 | snp | A/C | 1.67086e-05 | 0.00289033 | missense | ANAPC5 | GRCh38.p7 | 12:121319770 | AATGATATTTGCCAT[A/C]ATTCATTGCTCTGTC | 51433 |
rs779708700 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315268 | ATACAGAAAGCTACA[A/C]AACATTGTTGAAGTA | 51433 |
rs779723051 | snp | C/T | 1.65993e-05 | 0.00288086 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318651 | TGTTTTAACTAGTCA[C/T]TTTGAGGGTAAGAAT | 51433 |
rs780247790 | snp | C/T | 3.37496e-05 | 0.00410775 | missense | ANAPC5 | GRCh38.p7 | 12:121318372 | GGAGCATGGGCAGCG[C/T]GATGGTAGGGGAGGA | 51433 |
rs780254321 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341590 | GTGGCTGAATAGAGA[A/G]TGGTTAGATAAGTAA | 51433 |
rs780275154 | snp | A/G | | | utr-variant-3-prime | ANAPC5 | GRCh38.p7 | 12:121308419 | ATTTATAGGGAGAGA[A/G]GGGACATGAACAAGT | 51433 |
rs780370839 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350315 | GAGGCCCAGGGACCC[A/C]GATCTGTTTCTGCCA | 51433 |
rs780453419 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326556 | CTGCTCTTCTTTGGA[A/G]TCAACCAGGTTTCGG | 51433 |
rs780458618 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352863 | GAGCGATCCTCCCGC[C/T]TTCCCGAGAAGCTGG | 51433 |
rs780513001 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323613 | CTGGGATTACAAGTA[A/T]AAAGATAAACAGCAC | 51433 |
rs780693616 | snp | C/T | 6.67646e-05 | 0.00577736 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121319777 | TTTGCCATCATTCAT[C/T]GCTCTGTCAAACTGT | 51433 |
rs780753873 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | ANAPC5 | GRCh38.p7 | 12:121308551 | GGAAGAGCATCGCAC[A/G]CCGGTTCCTCTCCTG | 51433 |
rs780816219 | snp | A/G | 4.94409e-05 | 0.00497172 | stop-gained | ANAPC5 | GRCh38.p7 | 12:121320387 | AAAGGCAGATTACCT[A/G]GGCGTGCTGACTATT | 51433 |
rs781000401 | snp | C/G/T | 8.24727e-05 | 0.00642109 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318602 | AGCTTGTAATACAAC[C/G/T]GCTTTCCTGAAACAG | 51433 |
rs781113653 | in-del | -/AAA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319113 | ATGCTGTGTATACAC[-/AAA]CACACACACACACAC | 51433 |
rs781136062 | snp | C/T | 1.66098e-05 | 0.00288177 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318459 | CACAGGATGAGAAGA[C/T]CCACCACCACATCTC | 51433 |
rs781222122 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310069 | AAATATAGCAGGGGG[C/T]GGTTATTCACACTAT | 51433 |
rs781261846 | in-del | -/AAC | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313440 | AATGGAGACTAAGAG[-/AAC]AACAGAGAGAATCAA | 51433 |
rs781528879 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320671 | GCAGTGGCGCGATCT[C/T]GGCTCATTGCAAGCT | 51433 |
rs781662860 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348250 | TAAATAAGATAATAC[A/C]AAGTGCTTTGTAAAC | 51433 |
rs781772813 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321646 | TAGCAATTCTGATGT[C/T]TTAGCCCCCACCTCC | 51433 |
rs781783544 | snp | A/G | 1.65781e-05 | 0.00287902 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330571 | ACAATCTCACAGAAA[A/G]ATGAGCCTTACCGGT | 51433 |
rs781784460 | snp | C/T | 8.6722e-05 | 0.00658434 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327081 | AGAAGCACGTGGGCC[C/T]GGCCACCTGCCTACC | 51433 |
rs781786573 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324013 | CACTCTACCTCCTCT[A/G]GGTTGCAAGAGGAAG | 51433 |
rs781789108 | snp | C/T | 3.2962e-05 | 0.00405954 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335596 | CTCAAGCTCCGGCCA[C/T]AGCCCTCTTCCCCAT | 51433 |
rs781789951 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335601 | GCTCCGGCCATAGCC[C/T]TCTTCCCCATTACTT | 51433 |
rs781793559 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348968 | TATAATGCAGCCATT[-/A]AAAAGACCATTTGGG | 51433 |
rs781795735 | snp | C/T | 1.7621e-05 | 0.0029682 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335487 | CAGACTTTTTATTGT[C/T]ATCGGTTCCTTCAAT | 51433 |
rs781798986 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350158 | CCATGGTGTCCTCAG[A/T]TCTCCCCTCTTCCCA | 51433 |
rs781807742 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347647 | AAAGAAAAAGCTATC[C/T]ATTTTTCAACAAAAC | 51433 |
rs781808773 | snp | C/G | 1.70909e-05 | 0.00292321 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337432 | GTAGAAAGAAAGGGT[C/G]AATAAACATATGAAA | 51433 |
rs781810218 | snp | C/T | 4.97154e-05 | 0.0049855 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121327216 | CAACATCTGGGCCTG[C/T]TGCAGTGCCATGGTG | 51433 |
rs781814418 | snp | A/T | 1.95173e-05 | 0.00312383 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352105 | GTAAAAGTTTGCTGC[A/T]CGAGCAGGAGCCAGC | 51433 |
rs781815239 | snp | A/G | 1.66941e-05 | 0.00288908 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337242 | CAAACAAAAAAAGTT[A/G]CCTTGTCATTCCTTT | 51433 |
rs781816098 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334612 | TTTACTAAAACATAA[C/T]TGATCGATTTTCCTA | 51433 |
rs781822261 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333113 | CTGAGGTCAGGAGTT[C/T]GAGACCATCCTGACC | 51433 |
rs781824563 | snp | C/T | 1.66524e-05 | 0.00288547 | synonymous-codon, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331425 | GGCGAGCTCTGCCTG[C/T]TGACTAATGACAGAC | 51433 |
rs781825869 | snp | A/G | 1.80413e-05 | 0.00300338 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335759 | TGTATTTTAAACGCT[A/G]TAAATATCTCTGGTG | 51433 |
rs781826126 | snp | C/G | 1.65828e-05 | 0.00287943 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352212 | GCCTGTGCGGCTCAT[C/G]TCGTTCAGCAGCACC | 51433 |
rs781830174 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121328381 | GATGAGCTCTGACAG[A/G]CTGTGTTTCCAGTGC | 51433 |
rs781834515 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349042 | GGCTGAAGCAGGCAG[A/T]TTACTTGAGGTCAGG | 51433 |
rs781834980 | snp | A/C | 3.68012e-05 | 0.00428944 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352359 | GGCCCGAGACTAAGT[A/C]TCGGGCCCGCGGCGC | 51433 |
rs781836535 | snp | C/G | 1.69905e-05 | 0.00291461 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347008 | CATCAGTTTGATTCT[C/G]AATGAGAAAATCGAG | 51433 |
rs781838343 | snp | C/T | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354353 | GCGATGTTGTCCAGG[C/T]TGGTCTCGAACTCCT | 51433 |
rs781839878 | snp | A/G | 1.69392e-05 | 0.00291021 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345812 | TATTTCACAGGAAAA[A/G]GATCCCTGTCAGAAA | 51433 |
rs781843492 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347040 | TGCATATTTTAGAAA[-/G]GCCCTTTGAATAATT | 51433 |
rs781846678 | snp | A/G | 1.66863e-05 | 0.0028884 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337247 | AAAAAAAGTTGCCTT[A/G]TCATTCCTTTCCAAC | 51433 |
rs781847060 | snp | G/T | 1.64933e-05 | 0.00287165 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347886 | ATATCTGGGCCCTGT[G/T]TAAAGGAGAGATAGG | 51433 |
rs781848069 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345111 | AACAAGTTCCAAACA[C/T]AGCAGGGAGGAAGGA | 51433 |
rs781848730 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347338 | GTATGCTTAATGTTA[C/T]CCATTTTTCAGCCAG | 51433 |
rs781851547 | snp | C/T | 1.72958e-05 | 0.00294068 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352347 | GCTGGCCATGGCGGC[C/T]CGAGACTAAGTCTCG | 51433 |
rs781852620 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343777 | GCCTGCAATGCAGTA[A/T]ATAATAAGCTCCCAG | 51433 |
rs781855010 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335619 | TTCCCCATTACTTTT[A/G]CTTTCGGCTCCGGTA | 51433 |
rs781856610 | snp | A/C/T | 4.39264e-05 | 0.00468632 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346866 | ACTTCAATGAAAATA[A/C/T]TCTCTGCTCTTCTTA | 51433 |
rs781858140 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338697 | AAAACAAAAATCTTC[C/T]GCAATCTCACTACCC | 51433 |
rs781859411 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337245 | ACAAAAAAAGTTGCC[C/T]TGTCATTCCTTTCCA | 51433 |
rs781862210 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345768 | GTGAATTCTAAATGA[A/G]CAAGGACTTATTGCA | 51433 |
rs781862569 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352027 | ACGTTCCTCCAGGCA[A/G]GGAGAGTATCTGATG | 51433 |
rs781864612 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329301 | TGGGACTACAGGCGC[C/T]CACCACCACGCCCGG | 51433 |
rs781865469 | snp | A/C/T | 4.03529e-05 | 0.00449167 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330740 | CTAGTGAAATATCAA[A/C/T]GTGGTCATAAGAAAG | 51433 |
rs781870154 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334391 | TGTGAACACTATGCT[C/T]CCATTAATACACGCT | 51433 |
rs781870526 | in-del | -/GCACCAGGAAAGGAAGAGAAGTGATGTTA | 1.66953e-05 | 0.00288918 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327243 | GTGCTGGGTGGGGAG[lengthTooLong]AGGGAACAGGATTTC | 51433 |
rs781870840 | snp | C/G | 1.65416e-05 | 0.00287586 | missense | ANAPC5 | GRCh38.p7 | 12:121327185 | CATTCACCGCCTCCA[C/G]GCTGTTCATGCTCAG | 51433 |
rs781872182 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328948 | GGATGCCTATCATGA[-/G]CAACAAAATTATCTT | 51433 |
rs781876687 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327500 | CCCGCCCCCACCCCA[A/T]GTTCCCTGCAGTCAT | 51433 |
rs781877620 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350302 | ATCCCATAATATAGA[A/G]GCCCAGGGACCCAGA | 51433 |
rs781877821 | snp | A/C/T | 3.49878e-05 | 0.00418245 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327073 | ATTGCTCCAGAAGCA[A/C/T]GTGGGCCCGGCCACC | 51433 |
rs781881225 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346145 | CCTTCAGAAGAGTAA[G/T]AAAGAGACACTTGCA | 51433 |
rs781883342 | snp | A/G | 3.76343e-05 | 0.00433771 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347041 | GCATATTTTAGAAAG[A/G]CCCTTTGAATAATTT | 51433 |
rs781886255 | snp | A/G | 1.65592e-05 | 0.00287738 | intron-variant, synonymous-codon, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352223 | TCATCTCGTTCAGCA[A/G]CACCAGCACCGCGAT | 51433 |
rs781889281 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344702 | AGGGAGCACATGAGG[C/T]GAAAAGCCAGGGAAG | 51433 |
rs781899723 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334914 | AATGAAAGAGGCTAG[A/G]CACTAAGACGGCAAT | 51433 |
rs781901151 | snp | A/G | 3.49864e-05 | 0.00418234 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335501 | TCATCGGTTCCTTCA[A/G]TTTGCGCAAGGACAA | 51433 |
rs781904764 | snp | A/G | 3.32027e-05 | 0.00407434 | synonymous-codon, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331413 | TGCCTCCTGCAGGGC[A/G]AGCTCTGCCTGTTGA | 51433 |
rs781905187 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338636 | ATTATTATGTAGGTG[C/T]AGTATGGGGAAAAAT | 51433 |
rs781908008 | snp | C/T | 0.000153331 | 0.00875454 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345792 | TATTGCACTTGAAAT[C/T]ATACTATTTCACAGG | 51433 |
rs781908387 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326058 | CTTTCGACCTCAGAA[A/G]ACATGGGCAGTGCTT | 51433 |
rs781908394 | snp | A/G | 1.64914e-05 | 0.00287149 | missense | ANAPC5 | GRCh38.p7 | 12:121328343 | AGCCTCCAGATGGCC[A/G]TTTTCTGTGCGATGC | 51433 |
rs781909572 | snp | C/T | 1.66043e-05 | 0.00288129 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346983 | CCATATCCTTCAACT[C/T]GCCTTCAGCCATCAG | 51433 |
rs781909906 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337140 | GGAGAATCACTTGAA[C/G]CAGGGAGTCGGAGGT | 51433 |
rs781910898 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344340 | TCCCAGCACTTTGGG[A/G]GGCCAAGGCGGGTGG | 51433 |
rs781915895 | snp | G/T | 1.67936e-05 | 0.00289767 | intron-variant, missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121352178 | GCCTCCGCCGCTCCA[G/T]GAGGCTGACGGCGCC | 51433 |
rs781919903 | snp | A/C | 1.692e-05 | 0.00290856 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346025 | ATCATGTGACGCAGA[A/C]ACAAACCTACAAAAT | 51433 |
rs781920727 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349819 | TTCAAATGATTTCCT[G/T]CCTCAGCCTCCCGAG | 51433 |
rs781924805 | snp | A/G | 1.65553e-05 | 0.00287705 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346948 | AGAGAAAGAATCTGA[A/G]AGGTCATCAAAAAAC | 51433 |
rs781924871 | snp | C/T | 1.66424e-05 | 0.0028846 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121337378 | CTTAGTCTCATCATT[C/T]TTTAGCAAAGAAGCC | 51433 |
rs781924883 | snp | A/G | 1.72612e-05 | 0.00293774 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342074 | CCTCCTCTTCTCTGG[A/G]AAAAATAAAAAAACA | 51433 |
rs781926022 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355350 | TCACTTGAGGTCAGG[A/G]GCTCGAGACCAGCCT | 51433 |
rs781926469 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334220 | TGAGTTTGAGGTTAC[A/G]GTTAGCTATGATCAT | 51433 |
rs781928999 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348617 | TTGCAGTGAGCCAAG[A/G]TCACGCCATTGCACT | 51433 |
rs781931327 | snp | A/C | 1.68872e-05 | 0.00290574 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327273 | CCTTTCAGCAGCAGA[A/C]CTGGCTGCGCTTTGG | 51433 |
rs781931612 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327343 | TACACCTCACAGGCT[C/T]TGGCTTTCTTGGGAG | 51433 |
rs781931620 | in-del | -/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342813 | GCAGCGAGCCAAGAT[-/C]ACGCCACTGCACTCC | 51433 |
rs781931794 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355595 | TGGAGGTGGCGGCTC[A/G]TGCCTATAATCCCAG | 51433 |
rs781937762 | snp | C/G | 1.66156e-05 | 0.00288228 | missense | ANAPC5 | GRCh38.p7 | 12:121327119 | CGTGTAGCTCTGCGA[C/G]GTGGCAGAGTGCGAC | 51433 |
rs781940294 | snp | C/T | 1.64885e-05 | 0.00287123 | utr-variant-5-prime, missense | ANAPC5 | GRCh38.p7 | 12:121347881 | GTGTAATATCTGGGC[C/T]CTGTGTAAAGGAGAG | 51433 |
rs781948328 | snp | C/G/T | 1.87163e-05 | 0.00305905 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352380 | CCCGCGGCGCGCTGC[C/G/T]GCCAGTTGTCACCAC | 51433 |
rs781949407 | snp | C/T | 3.29527e-05 | 0.00405898 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345894 | CACCCTCATCTCTAC[C/T]GGTCAGTTCCATATC | 51433 |
rs781952269 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351378 | ACCCTGTCTCAAAAA[A/T]ATAATAATAATTTAA | 51433 |
rs781954005 | snp | A/G | 1.70904e-05 | 0.00292316 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328520 | GACAGATATACCCAC[A/G]ACCCAAGATAGAGAT | 51433 |
rs781954846 | in-del | -/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327907 | ACTCAACTAGAGCAA[-/C]CATGGATCATGCCTC | 51433 |
rs781955488 | snp | A/C/T | 8.31212e-05 | 0.00644628 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346927 | GTGAACCTCTGGTTC[A/C/T]GTTCCAGAGAAAGAA | 51433 |
rs781956453 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354190 | GATGGGGTTTCACCA[C/T]GTTGGCCCGGCTGGT | 51433 |
rs781958501 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343490 | CCAAGGTCTCAGAGA[A/C]CAAAGGCAGAGGAGC | 51433 |
rs781961401 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335412 | CTCACGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 51433 |
rs781963921 | in-del | -/A | 0.000239997 | 0.0109518 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342073 | CCTCCTCTTCTCTGG[-/A]AAAAAATAAAAAAAC | 51433 |
rs781969044 | snp | C/T | 1.65745e-05 | 0.00287871 | missense, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331397 | CCTGGGCAATCCTAA[C/T]TGCCTCCTGCAGGGC | 51433 |
rs781969756 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345451 | TACAGTCCCCAGGAC[C/T]GATAACAGTGGGGTA | 51433 |
rs781974176 | snp | C/T | 1.7483e-05 | 0.00295655 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330699 | AATCATCAAAATATA[C/T]CATAACAGTGGCAAT | 51433 |
rs781977557 | snp | A/G | 1.65952e-05 | 0.00288051 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335550 | GTGACCGAAGCGGCA[A/G]TGCAGGGCGGCAAGA | 51433 |
rs781977949 | snp | C/T | 8.25307e-05 | 0.00642328 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345864 | CATCAAGTTCTTCTT[C/T]TTCCATTTTTCTTTC | 51433 |
rs781978929 | snp | C/G | 1.65696e-05 | 0.00287828 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335717 | TGTTTAAGTAGCTGA[C/G]ATAATGCTAAAACAA | 51433 |
rs781984658 | snp | C/T | 1.65825e-05 | 0.00287941 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346001 | AAAGAAAGCTTACTG[C/T]AGGCCAAGATCATGT | 51433 |
rs781985504 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330367 | TGGTAAAGGGAATTT[C/G]CACAGATGTTATTAG | 51433 |
rs781986829 | snp | C/G | 1.66145e-05 | 0.00288218 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330670 | CAGCACATAAAGCCA[C/G]CTCTGGCAAGAGAAA | 51433 |
rs781990372 | snp | G/T | 1.6534e-05 | 0.00287519 | missense | ANAPC5 | GRCh38.p7 | 12:121327160 | TCTGTGTTGTTCTGC[G/T]GCACGCCCGCATTCA | 51433 |
rs781994470 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353782 | TAAATTATACTTTCT[C/T]TCTCTCTCATTCTGC | 51433 |
rs781999684 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344494 | GAGGTGGAGGCAGGA[C/G]AATCACTTGAACCCA | 51433 |
rs782000348 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346396 | CTTACACGTCCAGAG[C/G]CTGGCACATAGGAAG | 51433 |
rs782000715 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355424 | TAGCCAGGCATGGTG[A/G]GGGGTGCCTGTAATC | 51433 |
rs782002849 | snp | A/C | 1.66322e-05 | 0.00288371 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121337297 | AAGACTTACCGCTTC[A/C]GCAAAATCAGGATTA | 51433 |
rs782003788 | snp | A/T | 1.65548e-05 | 0.002877 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352309 | TTGGTCATCATGGGA[A/T]TGAAGTAGAGGCTCT | 51433 |
rs782005215 | snp | C/T | 1.64784e-05 | 0.00287035 | utr-variant-5-prime, synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121347849 | AGACTCTTCAATTAA[C/T]TTGTAAAGTTTTGAC | 51433 |
rs782005793 | snp | C/T | 6.67925e-05 | 0.00577856 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330551 | AGGCTCGACCATTTA[C/T]GGAAACAATCTCACA | 51433 |
rs782009148 | snp | C/T | 1.72788e-05 | 0.00293923 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331474 | TAATAATCACAAACA[C/T]GCATAAGCAACCATA | 51433 |
rs782011136 | in-del | -/C | 1.69112e-05 | 0.0029078 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345816 | TCACAGGAAAAGGAT[-/C]CCTGTCAGAAAAGCC | 51433 |
rs782011475 | snp | A/C/G | 5.03718e-05 | 0.00501834 | missense, synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121342041 | CTTGTTTTTGGGACA[A/C/G]AGGCCCACTGCAAGA | 51433 |
rs782012718 | snp | A/G | 1.67654e-05 | 0.00289524 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121342010 | TCACATACCTGTTGA[A/G]AAAGAAAAAATTCTG | 51433 |
rs782012994 | snp | C/T | 3.56595e-05 | 0.00422238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330705 | CAAAATATATCATAA[C/T]AGTGGCAATGGCTGA | 51433 |
rs782013690 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325570 | TTCTATTCTAATAGT[A/G]AAAAAAAATAATTTC | 51433 |
rs782014585 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336766 | TCAGGAGGATGATGA[C/T]TGAAAGAGAACATCA | 51433 |
rs782021131 | snp | C/T | 5.12877e-05 | 0.00506372 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331468 | TCCCATTAATAATCA[C/T]AAACATGCATAAGCA | 51433 |
rs782021422 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328796 | TTAGGGCCAGTCACT[C/T]AGCTTCTTAGCTAAG | 51433 |
rs782022766 | snp | C/T | 1.6504e-05 | 0.00287258 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335573 | CGGCAAGATTCAGAG[C/T]GGCGTATCTCAAGCT | 51433 |
rs782028408 | snp | C/T | 0.00106213 | 0.0230204 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351207 | AAAATCCCGTCTCTA[C/T]AAAAAATGCAAAAAA | 51433 |
rs782029328 | snp | A/C | 1.81099e-05 | 0.00300909 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346052 | AAATAAGACGAGAGA[A/C]AAGGGGAAAGCATTA | 51433 |
rs782034850 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345591 | CCCCCAAGAAAGGGA[A/G]CCAATGAATCCACAC | 51433 |
rs782041455 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350183 | TTCCCATGCCCCTCA[C/G]CCACAAATACAAGTG | 51433 |
rs782047843 | snp | A/G | 4.96225e-05 | 0.00498084 | missense | ANAPC5 | GRCh38.p7 | 12:121327169 | TTCTGCTGCACGCCC[A/G]CATTCACCGCCTCCA | 51433 |
rs782059026 | snp | A/T | 1.76646e-05 | 0.00297186 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330702 | CATCAAAATATATCA[A/T]AACAGTGGCAATGGC | 51433 |
rs782059421 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343537 | GATCTGACTGCAGAG[C/G]CAGACTCTTAACTCC | 51433 |
rs782060499 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349003 | GGCGCAGTGGCTCAC[A/G]CCTGTAATACCAGCG | 51433 |
rs782064195 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351569 | TTCTAGCGATTCTCC[G/T]GCCTCAGCCTCCCGA | 51433 |
rs782064940 | snp | A/C/G | 5.31772e-05 | 0.00515618 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346046 | CCTACAAAATAAGAC[A/C/G]AGAGACAAGGGGAAA | 51433 |
rs782065672 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344651 | TGGTCAGGGAGGCCC[A/G]TCTGAGGAAAGTTGA | 51433 |
rs782067427 | snp | A/T | 1.64963e-05 | 0.00287192 | missense | ANAPC5 | GRCh38.p7 | 12:121328338 | CATACAGCCTCCAGA[A/T]GGCCGTTTTCTGTGC | 51433 |
rs782069188 | snp | A/G | 1.78557e-05 | 0.0029879 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342092 | AAATAAAAAAACAAA[A/G]ATAGTAAAGAATTAC | 51433 |
rs782069827 | snp | G/T | 1.65512e-05 | 0.00287669 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346950 | AGAAAGAATCTGAAA[G/T]GTCATCAAAAAACTG | 51433 |
rs782071849 | snp | C/T | 3.52367e-05 | 0.00419727 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335490 | ACTTTTTATTGTCAT[C/T]GGTTCCTTCAATTTG | 51433 |
rs782072125 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337079 | AAAAATTAGCTGGGC[A/G]TGGTGGCACGTGCCT | 51433 |
rs782074122 | snp | A/C | 1.66754e-05 | 0.00288746 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121337389 | CATTCTTTAGCAAAG[A/C]AGCCTGAAATTTAAA | 51433 |
rs782075258 | snp | A/G | 1.6775e-05 | 0.00289607 | intron-variant, synonymous-codon, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352182 | CCGCCGCTCCATGAG[A/G]CTGACGGCGCCCTCG | 51433 |
rs782078333 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339557 | CTCACTGCAAACTCC[A/G]CCTCATGGGTTCAAG | 51433 |
rs782081656 | in-del | -/A | 1.65471e-05 | 0.00287633 | frameshift-variant, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346956 | ATCTGAAAGGTCATC[-/A]AAAAAACTGTTCCAT | 51433 |
rs782082076 | snp | A/T | 3.32254e-05 | 0.00407573 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121337348 | TTCCTTCTGCAAGGA[A/T]GCTGGAGTGAGGGCC | 51433 |
rs782082544 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331143 | TTGTAGAGCAGATAT[A/T]TGCCAAAAGCAAAAC | 51433 |
rs782083011 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334145 | AAAATTAGCTGGGCA[C/T]TGTGGTGCATGCCTG | 51433 |
rs782083815 | snp | A/G | 0.00043376 | 0.0147205 | intron-variant, synonymous-codon, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352326 | GAAGTAGAGGCTCTC[A/G]TGGACGCTGGCCATG | 51433 |
rs782088848 | snp | A/C | 1.78931e-05 | 0.00299102 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331480 | TCACAAACATGCATA[A/C]GCAACCATAGCAGGA | 51433 |
rs782091990 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329053 | TTGTAGTTAAGCCTG[A/C]GCTTACTTCAAGGAG | 51433 |
rs782092193 | snp | A/G | 1.66969e-05 | 0.00288932 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330552 | GGCTCGACCATTTAT[A/G]GAAACAATCTCACAG | 51433 |
rs782095323 | snp | C/T | 4.97335e-05 | 0.00498641 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352214 | CTGTGCGGCTCATCT[C/T]GTTCAGCAGCACCAG | 51433 |
rs782098688 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350069 | ATGCATTTATAGTAA[C/T]AGCAGACGTGGCTAG | 51433 |
rs782099164 | snp | C/T | 1.81427e-05 | 0.00301182 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335760 | GTATTTTAAACGCTG[C/T]AAATATCTCTGGTGT | 51433 |
rs782100359 | snp | C/T | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355471 | CTGAGGCAGGAGGAT[C/T]GGTTGAACCCAGGAG | 51433 |
rs782104727 | snp | A/G | 1.84191e-05 | 0.00303467 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346056 | AAGACGAGAGACAAG[A/G]GGAAAGCATTAACTG | 51433 |
rs782106239 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345769 | TGAATTCTAAATGAA[A/C]AAGGACTTATTGCAC | 51433 |
rs782106616 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352071 | CCAAGCCCAGGGTTC[C/T]GCACAGAGCAGATGC | 51433 |
rs782110095 | snp | A/T | 5.02382e-05 | 0.00501164 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337401 | AAGAAGCCTGAAATT[A/T]AAAAATGGTAACTCA | 51433 |
rs782113808 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333042 | TATTTGTGGCCGGGC[A/G]CAGTGGCTCACGCCT | 51433 |
rs782114192 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344516 | TTGAACCCAGGAGGT[A/G]GAGGTTGCAGTGAGT | 51433 |
rs782114966 | snp | C/T | 7.21436e-05 | 0.00600555 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335757 | AATGTATTTTAAACG[C/T]TGTAAATATCTCTGG | 51433 |
rs782118615 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327536 | GTTAATTAGTTTTCA[C/T]GGGTGAATTCAGACC | 51433 |
rs782120209 | snp | G/T | 1.66156e-05 | 0.00288228 | missense, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331417 | TCCTGCAGGGCGAGC[G/T]CTGCCTGTTGACTAA | 51433 |
rs782120409 | snp | A/C | 1.66871e-05 | 0.00288847 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346993 | CAACTCGCCTTCAGC[A/C]ATCAGTTTGATTCTG | 51433 |
rs782121964 | snp | A/G | 1.6777e-05 | 0.00289624 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330542 | AAGAGACAAAGGCTC[A/G]ACCATTTATGGAAAC | 51433 |
rs782122962 | snp | A/C | 1.66738e-05 | 0.00288732 | intron-variant, stop-gained, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352196 | GGCTGACGGCGCCCT[A/C]GCCTGTGCGGCTCAT | 51433 |
rs782125510 | snp | C/T | 1.65776e-05 | 0.00287898 | missense, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331375 | AGACACACGTGATCG[C/T]TGGACTCCTGGGCAA | 51433 |
rs782126050 | snp | G/T | 1.66142e-05 | 0.00288216 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328298 | GAATTCACACCCCCA[G/T]GGCCTTGGGAGACCT | 51433 |
rs782127593 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336871 | CCAAGAACACGATTT[C/T]CTTCAAGAACCTGGG | 51433 |
rs782131361 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353988 | CATGCATGGCTAATT[-/T]TTTTTTTTTTTTTTT | 51433 |
rs782132363 | snp | C/T | 1.73396e-05 | 0.0029444 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352348 | CTGGCCATGGCGGCC[C/T]GAGACTAAGTCTCGG | 51433 |
rs782134243 | snp | C/T | 3.30704e-05 | 0.00406622 | missense | ANAPC5 | GRCh38.p7 | 12:121327164 | TGTTGTTCTGCTGCA[C/T]GCCCGCATTCACCGC | 51433 |
rs782134306 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346828 | TAGCAGAACAATGAT[-/A]GACATGACTTAGAAA | 51433 |
rs782135648 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328865 | TCATAAAGAATTATC[A/G]TAAGGATTACAATGA | 51433 |
rs782136344 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347259 | TCAATTATCTGCAAT[G/T]ACTAAAAAGAGTAAG | 51433 |
rs782138935 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351835 | CCCTGTGTCTCCAAC[C/G]CTCTATTGTATAGCC | 51433 |
rs782140250 | snp | A/G | 1.64906e-05 | 0.00287142 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347884 | TAATATCTGGGCCCT[A/G]TGTAAAGGAGAGATA | 51433 |
rs782143236 | snp | C/T | | | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352340 | CGTGGACGCTGGCCA[C/T]GGCGGCCCGAGACTA | 51433 |
rs782144653 | snp | C/T | 1.68403e-05 | 0.0029017 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328265 | GAACCAGCTTGCTAG[C/T]TCCTGCTTCTCTCTA | 51433 |
rs782146233 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345612 | GAATCCACACTCCAC[A/G]TCATTCTCCCTGGCC | 51433 |
rs782147469 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341636 | TATTAATTGTAGAAT[C/T]GAGGTAATAGGTATG | 51433 |
rs782154458 | snp | G/T | 1.86048e-05 | 0.00304993 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330718 | AACAGTGGCAATGGC[G/T]GATGTTCTAGTGAAA | 51433 |
rs782157779 | snp | A/G | 1.65384e-05 | 0.00287557 | missense | ANAPC5 | GRCh38.p7 | 12:121327178 | ACGCCCGCATTCACC[A/G]CCTCCAGGCTGTTCA | 51433 |
rs782159197 | snp | A/T | 1.67787e-05 | 0.00289639 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121342031 | AAAAATTCTGCTTGT[A/T]TTTGGGACAGAGGCC | 51433 |
rs782160562 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335610 | ATAGCCCTCTTCCCC[A/G]TTACTTTTGCTTTCG | 51433 |
rs782160830 | snp | C/T | 1.64857e-05 | 0.00287099 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345875 | TCTTTTTCCATTTTT[C/T]TTTCACCCTCATCTC | 51433 |
rs782165073 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327389 | GCCAGCAACCTTGCC[C/T]TCAGGATAAGAAAGG | 51433 |
rs782171182 | snp | A/C/T | 3.30454e-05 | 0.0040647 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352280 | TGCCGAACACATTGG[A/C/T]GTGCACAACCCCATT | 51433 |
rs782172573 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338283 | CTAATTCCATTGTTA[A/G]TTTATGTCATTATAG | 51433 |
rs782174446 | snp | A/G | 2.11943e-05 | 0.00325526 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346872 | ATGAAAATACTCTCT[A/G]CTCTTCTTAGAAGAG | 51433 |
rs782176493 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343939 | GAAATACATACATAT[A/C]TTTTTGCCTGCAAGT | 51433 |
rs782177661 | snp | C/T | 1.65113e-05 | 0.00287322 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352374 | CTCGGGCCCGCGGCG[C/T]GCTGCCGCCAGTTGT | 51433 |
rs782179450 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351171 | AGTCCAGGAGTTCCC[A/G]GCCAGCCTGGGTAAC | 51433 |
rs782180743 | snp | A/C | 1.6552e-05 | 0.00287676 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335558 | AGCGGCAGTGCAGGG[A/C]GGCAAGATTCAGAGC | 51433 |
rs782183222 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346388 | ATGTCTATCTTACAC[A/G]TCCAGAGCCTGGCAC | 51433 |
rs782184445 | snp | A/C | 1.64776e-05 | 0.00287028 | utr-variant-5-prime, missense | ANAPC5 | GRCh38.p7 | 12:121347833 | TTGCCAGCTGTGGAC[A/C]AGACTCTTCAATTAA | 51433 |
rs782189163 | snp | A/C | 1.64988e-05 | 0.00287213 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345868 | AAGTTCTTCTTTTTC[A/C]ATTTTTCTTTCACCC | 51433 |
rs782190228 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328132 | AAGAAGGAACATGCA[C/T]GGGAAAAAAGTTTTC | 51433 |
rs782190762 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333994 | TAAAGCCTCACAACT[A/G]GGTTGGCCCAGTGGC | 51433 |
rs782193704 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337479 | ATCACCTGATTATTT[G/T]CTTTTCTACAGGGGT | 51433 |
rs782198385 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326692 | TGAAGTGGATTCTAT[C/G]AGACAGTACCCATAA | 51433 |
rs782203591 | snp | C/T | 1.68374e-05 | 0.00290145 | intron-variant, missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121352171 | TGGTTGAGCCTCCGC[C/T]GCTCCATGAGGCTGA | 51433 |
rs782209689 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337987 | AATTATATAAAATAT[A/G]TAGAAAGTTAGCTAC | 51433 |
rs782210294 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324793 | TGTAGTCCCAGCTAC[C/T]AGGCAGGTTGAGGTG | 51433 |
rs782210508 | snp | A/T | 1.67279e-05 | 0.002892 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346014 | TGTAGGCCAAGATCA[A/T]GTGACGCAGAAACAA | 51433 |
rs782213818 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352427 | GGGTCTACATCTCCG[C/G]CCGCCCTCACAATAT | 51433 |
rs782216638 | snp | A/C | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355238 | TTATTCCTAGATGGT[A/C]ACAACTGACTGGATA | 51433 |
rs782217687 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336400 | ACTGTCATTTAGGCT[A/G]GGCGTGATGGCTCAT | 51433 |
rs782220730 | snp | C/T | 1.68091e-05 | 0.00289901 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327266 | AGGATTTCCTTTCAG[C/T]AGCAGACCTGGCTGC | 51433 |
rs782220937 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332469 | GAAAACAAGAGCACT[A/T]CACCTTCACTTTCTA | 51433 |
rs782229596 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346298 | GGCTGTTACACTATC[C/T]GAAATGATATTTATG | 51433 |
rs782230328 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325034 | AGCTGTGTGGTAGCA[C/T]GCTCCTATAGTCTCA | 51433 |
rs782235948 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334962 | GGGGGCAGACTATTT[A/G]GGCAGAAGGTTTTCA | 51433 |
rs782240354 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351272 | CAGCTACTTGGGAGG[C/G]TGAGGTGGGAGGATC | 51433 |
rs782244195 | snp | C/T | 1.6661e-05 | 0.00288621 | intron-variant, missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121328491 | GTATTCCCAGGGAGG[C/T]GAGGTACTAAGGGGA | 51433 |
rs782249972 | in-del | -/AG | 1.69029e-05 | 0.00290709 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341972 | CAGGACTAGAACAGA[-/AG]AGTTCATGATAAATT | 51433 |
rs782251288 | snp | C/T | 1.6604e-05 | 0.00288127 | splice-acceptor-variant | ANAPC5 | GRCh38.p7 | 12:121335725 | TAGCTGAGATAATGC[C/T]AAAACAAGAAATAAT | 51433 |
rs782251690 | snp | A/G | 1.66953e-05 | 0.00288918 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327243 | GGTGCTGGGTGGGGA[A/G]AGGGAACAGGATTTC | 51433 |
rs782255870 | snp | A/T | 1.65392e-05 | 0.00287564 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347776 | CTTCACACCTTTTCA[A/T]ATATAAAGAAGAAAA | 51433 |
rs782262540 | snp | G/T | 1.68972e-05 | 0.0029066 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341974 | AGGACTAGAACAGAA[G/T]TTCATGATAAATTAC | 51433 |
rs782267122 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334106 | CAAAGCAAGATCCTA[C/T]CTCTACAAAAAATAA | 51433 |
rs782267730 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344283 | GGAGGAATAAAGAAA[C/T]AGAAAGTATTTGGGG | 51433 |
rs782268869 | snp | C/T | 0.0004111 | 0.0143311 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351074 | CCTGTGTCTGCAAAA[C/T]GAAATAACACATGAC | 51433 |
rs782269270 | snp | C/G | 1.66443e-05 | 0.00288477 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345839 | GAAAAGCCAAATTAC[C/G]TTACAGATACATCAA | 51433 |
rs782270838 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339305 | ATCCACCTGCCTCTG[A/C]CTCCCAAAGTGCTGG | 51433 |
rs782272516 | snp | A/G | 1.65996e-05 | 0.00288089 | synonymous-codon, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331368 | GTGCTGGAGACACAC[A/G]TGATCGTTGGACTCC | 51433 |
rs782275374 | snp | A/C | 1.65446e-05 | 0.00287612 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330660 | TCTTCTGCCCCAGCA[A/C]ATAAAGCCAGCTCTG | 51433 |
rs782278207 | snp | C/T | 1.65375e-05 | 0.0028755 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347908 | AGAGATAGGGAGGTA[C/T]GGATTTTAAAGAGCT | 51433 |
rs782285246 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345965 | TGCTGAAGGGCAGTG[C/T]ACAGTTTAAACACTT | 51433 |
rs782286059 | snp | C/T | 1.68388e-05 | 0.00290158 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121327102 | CCTGCCTACCTGCTC[C/T]GCGTGTAGCTCTGCG | 51433 |
rs782288482 | in-del | -/T | 1.76247e-05 | 0.00296851 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331478 | AATCACAAACATGCA[-/T]AAGCAACCATAGCAG | 51433 |
rs782291208 | snp | A/G | 1.8479e-05 | 0.0030396 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346887 | GCTCTTCTTAGAAGA[A/G]TTTCATACCTACTAC | 51433 |
rs782291524 | snp | A/G | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352887 | AAGCTGGGACTACAG[A/G]CAGCGCGCCTGGCTT | 51433 |
rs782292084 | snp | A/C | 1.64781e-05 | 0.00287033 | utr-variant-5-prime, missense | ANAPC5 | GRCh38.p7 | 12:121347843 | TGGACAAGACTCTTC[A/C]ATTAACTTGTAAAGT | 51433 |
rs782293524 | snp | A/C | 1.69893e-05 | 0.00291451 | intron-variant, missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121352155 | CAGGGGCAGGAGCAG[A/C]TGGTTGAGCCTCCGC | 51433 |
rs782296148 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342938 | TGTAAGTACATCCTA[C/T]AAAATAAAAAGGTTC | 51433 |
rs782297405 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340317 | GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 51433 |
rs782298804 | snp | A/G | 1.681e-05 | 0.00289909 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327267 | GGATTTCCTTTCAGC[A/G]GCAGACCTGGCTGCG | 51433 |
rs782300017 | snp | C/T | 6.6131e-05 | 0.00574988 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352294 | GCGTGCACAACCCCA[C/T]TGGTCATCATGGGAT | 51433 |
rs782305483 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334054 | GCCAAGGTGGGAGGA[C/T]TGCTGGAAGCCAGGA | 51433 |
rs782307103 | snp | A/T | 1.69937e-05 | 0.00291488 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331463 | TAATATCCCATTAAT[A/T]ATCACAAACATGCAT | 51433 |
rs782308445 | snp | A/G | 1.66499e-05 | 0.00288525 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337282 | CAACAAATTCTGGGA[A/G]AGACTTACCGCTTCA | 51433 |
rs782309178 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351644 | TTGTGTTTTTAGTAG[A/G]GACGGGGTTTCACTA | 51433 |
rs782311213 | snp | A/G | 6.65358e-05 | 0.00576745 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121327117 | CGCGTGTAGCTCTGC[A/G]AGGTGGCAGAGTGCG | 51433 |
rs782311751 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342080 | TTCTCTGGAAAAAAT[-/A]AAAAAAACAAAAATA | 51433 |
rs782316918 | snp | C/T | 1.6804e-05 | 0.00289858 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331338 | CCCAAGACCAGAGGA[C/T]GGCCTCACCAAACAG | 51433 |
rs782317893 | snp | A/T | 1.68547e-05 | 0.00290294 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341983 | ACAGAAGTTCATGAT[A/T]AATTACAGAATTCAC | 51433 |
rs782322052 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345476 | GGGGTACCTTTCACC[G/T]GGGGCCTGCAAACAC | 51433 |
rs782322833 | snp | C/T | 2.05818e-05 | 0.00320788 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346875 | AAAATACTCTCTGCT[C/T]TTCTTAGAAGAGTTT | 51433 |
rs782326181 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355319 | CCCAACATTTTGGGA[A/G]GCCAAGGCAGGCAGA | 51433 |
rs782328332 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334161 | TGTGGTGCATGCCTG[C/T]AGTCACAGCTAGGAG | 51433 |
rs782328672 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349582 | AAAAAAATTAAAAAA[A/T]AAATAAATTTAAAAA | 51433 |
rs782328894 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338106 | GGGCAGGGTGTGGTG[C/G]TTGATGCCTGTAATC | 51433 |
rs782330075 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344326 | GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 51433 |
rs782330692 | snp | A/G | 1.64776e-05 | 0.00287028 | utr-variant-5-prime, missense | ANAPC5 | GRCh38.p7 | 12:121347836 | CCAGCTGTGGACAAG[A/G]CTCTTCAATTAACTT | 51433 |
rs782335317 | snp | C/T | 4.9597e-05 | 0.00497956 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347778 | TCACACCTTTTCATA[C/T]ATAAAGAAGAAAATG | 51433 |
rs782336229 | snp | C/T | 1.65718e-05 | 0.00287848 | synonymous-codon, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331380 | CACGTGATCGTTGGA[C/T]TCCTGGGCAATCCTA | 51433 |
rs782337541 | snp | C/G | 1.66352e-05 | 0.00288398 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335730 | GAGATAATGCTAAAA[C/G]AAGAAATAATCAATG | 51433 |
rs782339225 | snp | C/T | | | missense | ANAPC5 | GRCh38.p7 | 12:121327230 | GTTGCAGTGCCATGG[C/T]GCTGGGTGGGGAGAG | 51433 |
rs782339756 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340722 | CACACCCGGCTAATT[G/T]TTGTGTGTGTGTTTT | 51433 |
rs782343418 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346342 | CAACTGGCTCCCCCA[A/G]CCAGAGGTAATCTCC | 51433 |
rs782345635 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335068 | TCTTCTTTTTAAAAA[A/G]TACATTTTTTAAAAA | 51433 |
rs782346740 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325132 | TTGCACCACTACATT[A/C]CAGCCCTGGTGATAC | 51433 |
rs782351097 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329930 | AGATAAGCCTTTTCA[A/G]TGCCCCTCTGTGTAT | 51433 |
rs782351807 | snp | G/T | 1.65162e-05 | 0.00287365 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345859 | AGATACATCAAGTTC[G/T]TCTTTTTCCATTTTT | 51433 |
rs782352375 | snp | A/G | 6.72325e-05 | 0.00579756 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346018 | GGCCAAGATCATGTG[A/G]CGCAGAAACAAACCT | 51433 |
rs782358237 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346810 | TGTGTCTGTTCACAG[A/T]TATAGCAGAACAATG | 51433 |
rs782359375 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351367 | GACAAAGCGAGACCC[C/T]GTCTCAAAAAAATAA | 51433 |
rs782361297 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328057 | GATGTGTGAACCCTG[A/G]TTTACTCTCCCAGCA | 51433 |
rs782361863 | snp | A/G | 1.6574e-05 | 0.00287867 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346940 | TCAGTTCCAGAGAAA[A/G]AATCTGAAAGGTCAT | 51433 |
rs782362477 | snp | A/T | 1.66125e-05 | 0.00288201 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121337354 | CTGCAAGGAAGCTGG[A/T]GTGAGGGCCTTAGTC | 51433 |
rs782363356 | in-del | -/T | 1.67778e-05 | 0.00289631 | frameshift-variant, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121342030 | AAAAAATTCTGCTTG[-/T]TTTTGGGACAGAGGC | 51433 |
rs782369727 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335232 | GTGCAATGGCGTGCT[C/T]TCGGCTCACTGCAAC | 51433 |
rs782370072 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354164 | CGGCTAATTTTTGTA[C/T]TGTTTGTAGAGATGG | 51433 |
rs782375551 | snp | A/G | 3.32768e-05 | 0.00407888 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121337292 | TGGGAAAGACTTACC[A/G]CTTCAGCAAAATCAG | 51433 |
rs782375575 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328891 | AATGAAATAATAGAT[A/G]TCAAACAGTGCTGCG | 51433 |
rs782378833 | snp | A/G | 1.72692e-05 | 0.00293842 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331473 | TTAATAATCACAAAC[A/G]TGCATAAGCAACCAT | 51433 |
rs782378935 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334108 | AAGCAAGATCCTACC[G/T]CTACAAAAAATAATT | 51433 |
rs782378980 | snp | C/T | 3.2956e-05 | 0.00405918 | utr-variant-5-prime, missense | ANAPC5 | GRCh38.p7 | 12:121347845 | GACAAGACTCTTCAA[C/T]TAACTTGTAAAGTTT | 51433 |
rs782379679 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344300 | GAAAGTATTTGGGGC[C/T]GAGTGCGGTGGCTCA | 51433 |
rs782379843 | snp | A/G | 1.65367e-05 | 0.00287543 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352300 | ACAACCCCATTGGTC[A/G]TCATGGGATTGAAGT | 51433 |
rs782383098 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339473 | GCCTTTTAATTTTTT[A/C]ATTTTATTTCTTTTT | 51433 |
rs782384066 | in-del | -/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339054 | ATATGACTTTTTTTT[-/C]TTTTTTTTTTTTTTT | 51433 |
rs782384727 | snp | A/G | | | missense | ANAPC5 | GRCh38.p7 | 12:121327128 | CTGCGAGGTGGCAGA[A/G]TGCGACAGCAAAGGA | 51433 |
rs782385414 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324899 | AAAAATAAAAAATAC[A/G]CTGGGTGTGGTAATC | 51433 |
rs782388495 | in-del | -/A | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352354 | TGGCGGCCCGAGACT[-/A]AAGTCTCGGGCCCGC | 51433 |
rs782390170 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332210 | TCAAGCGATCCTCCT[C/T]CTTTGGCCTCCCAAA | 51433 |
rs782392192 | snp | C/T | 3.41518e-05 | 0.00413216 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328519 | GGACAGATATACCCA[C/T]GACCCAAGATAGAGA | 51433 |
rs782399124 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348667 | AAGACTCCGTCTCCA[A/G]TAAAAAAAAAAGAGT | 51433 |
rs782406921 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355392 | TGAAACCCTGTCTCT[A/G]TTAAAAATATAAAAA | 51433 |
rs782408658 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342968 | CTCTAACAAAGTAAT[C/T]TCTTTTAGACAAAGA | 51433 |
rs782409424 | snp | A/G | 1.65146e-05 | 0.0028735 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335700 | ATCTTGGACACGGAG[A/G]TTGTTTAAGTAGCTG | 51433 |
rs782410889 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341021 | AATGAAAAAATATGG[C/T]TGAAAAGCATCCATA | 51433 |
rs782414769 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336447 | CTTTGGGAGGCCGAG[A/G]AGGGTGGATCACCTG | 51433 |
rs782415180 | snp | A/C/G | 4.97437e-05 | 0.00498696 | missense, synonymous-codon, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331374 | GAGACACACGTGATC[A/C/G]TTGGACTCCTGGGCA | 51433 |
rs782416834 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351189 | CAGCCTGGGTAACAT[A/G]GCAAAATCCCGTCTC | 51433 |
rs782418596 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338820 | AAAAATATGTGTATA[C/T]ATATTATATAAATTT | 51433 |
rs782420273 | snp | C/T | 1.67156e-05 | 0.00289093 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328288 | TCTCTCTAAAGAATT[C/T]ACACCCCCAGGGCCT | 51433 |
rs782424843 | snp | C/T | 1.8541e-05 | 0.00304469 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352361 | CCCGAGACTAAGTCT[C/T]GGGCCCGCGGCGCGC | 51433 |
rs782427866 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345350 | AGAAAACAAAGAACA[C/T]ATTCAAATTGAGTAG | 51433 |
rs782429238 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330316 | TGTGCTAAATTAATG[-/T]TGCTCAATAAACTAA | 51433 |
rs782438051 | snp | C/T | 1.65902e-05 | 0.00288008 | stop-gained, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330667 | CCCCAGCACATAAAG[C/T]CAGCTCTGGCAAGAG | 51433 |
rs782441636 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335121 | AATTCATTTCTTCCA[C/T]TTCTTTTCCCTTTTC | 51433 |
rs782442480 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332024 | TTTTTTAAAAATAGA[C/T]ATAGAGTCTCACTAT | 51433 |
rs782442851 | snp | A/G | 4.95626e-05 | 0.00497784 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347902 | TAAAGGAGAGATAGG[A/G]AGGTATGGATTTTAA | 51433 |
rs782444009 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338557 | TCACGCCACTGCACT[A/C]CAGCCTGGGTGACAG | 51433 |
rs782445257 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335643 | TCCGGTAAGAATCAG[A/G]CGATCAAAATAATGG | 51433 |
rs782445374 | snp | G/T | 1.6476e-05 | 0.00287014 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345943 | TTTCTCACCATTCTG[G/T]AAGTACTGCTGAAGG | 51433 |
rs782445493 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336086 | TAAAACCTGAATTCA[C/T]ATACAAATTATAAAA | 51433 |
rs782446439 | snp | A/T | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335605 | CGGCCATAGCCCTCT[A/T]CCCCATTACTTTTGC | 51433 |
rs782447912 | snp | A/G | 3.62345e-05 | 0.00425628 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347028 | AGAAAATCGAGGTGC[A/G]TATTTTAGAAAGGCC | 51433 |
rs782455496 | snp | A/G | 1.70577e-05 | 0.00292037 | intron-variant, synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121352143 | TCTCACCTGCAGCAG[A/G]GGCAGGAGCAGCTGG | 51433 |
rs782459617 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331239 | AACTTGTTTCCTTTT[A/G]CTGCTGAAGATCTCT | 51433 |
rs782461046 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325932 | CTTCTCTTATCCAAG[A/G]CACCAGGAAAGGAAG | 51433 |
rs782463114 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354401 | CTGCCTCAGCCTCCC[A/G]AATTGCTACGATTAA | 51433 |
rs782472022 | snp | C/G/T | 3.74295e-05 | 0.00432592 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352372 | GTCTCGGGCCCGCGG[C/G/T]GCGCTGCCGCCAGTT | 51433 |
rs782477271 | snp | A/C | 1.65241e-05 | 0.00287433 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352254 | CTTGTACGGCGTCAC[A/C]CAGTCCTTGATGCCG | 51433 |
rs782477474 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349140 | AAGTGATCCTCCCAC[A/G]TTGGCCTCCCAAAGT | 51433 |
rs782477759 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348393 | GAGAGGCCGGGCACA[-/T]GTGGCTCATGCCTAT | 51433 |
rs782478417 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343898 | CTTCCTCACCAGATC[A/G]CAGGCTCTTTGACAT | 51433 |
rs782480729 | snp | C/T | 1.65419e-05 | 0.00287588 | missense | ANAPC5 | GRCh38.p7 | 12:121327190 | ACCGCCTCCAGGCTG[C/T]TCATGCTCAGCAACA | 51433 |
rs782483578 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338701 | CAAAAATCTTCTGCA[A/G]TCTCACTACCCAGAA | 51433 |
rs782484553 | snp | C/G | 1.68281e-05 | 0.00290065 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337409 | TGAAATTTAAAAATG[C/G]TAACTCAGTAGAAAG | 51433 |
rs782488179 | snp | C/T | 1.65091e-05 | 0.00287303 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330643 | AACATAGCTATCGGA[C/T]CTCTTCTGCCCCAGC | 51433 |
rs782492260 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335795 | CAACTGCAGAGAGTT[C/T]CACTGTCTACAAACA | 51433 |
rs782498102 | snp | G/T | 1.74775e-05 | 0.00295608 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335502 | CATCGGTTCCTTCAA[G/T]TTGCGCAAGGACAAA | 51433 |
rs782498524 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329398 | ACCTCACGATCCACC[C/T]GCCTTGGCCTCCCAA | 51433 |
rs782502655 | snp | C/T | 1.65061e-05 | 0.00287277 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330612 | GTACTGCCTTCTTCA[C/T]AGAATGCTCCAGCAG | 51433 |
rs782502769 | snp | C/G | 1.66751e-05 | 0.00288744 | splice-acceptor-variant, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331429 | AGCTCTGCCTGTTGA[C/G]TAATGACAGACTAAA | 51433 |
rs782505196 | snp | C/T | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354768 | GAAAAAGCATACTTA[C/T]AATCTCCCAGCTCTT | 51433 |
rs782507541 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346267 | CACCTGAAGGCTTCC[A/G]TTTTACTTTCTTCAT | 51433 |
rs782510028 | snp | A/G | 0.000922722 | 0.0214595 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121328366 | TGCGATGCTGATATC[A/G]ATGAGCTCTGACAGG | 51433 |
rs782511138 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324558 | CAGAAAAAAAAGACA[C/T]AAAATTCTAACAAAT | 51433 |
rs782511441 | snp | A/G | 3.36095e-05 | 0.00409922 | missense | ANAPC5 | GRCh38.p7 | 12:121327103 | CTGCCTACCTGCTCC[A/G]CGTGTAGCTCTGCGA | 51433 |
rs782513087 | snp | A/C | | | intron-variant, synonymous-codon, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352224 | CATCTCGTTCAGCAG[A/C]ACCAGCACCGCGATC | 51433 |
rs782517850 | snp | C/T | 1.71817e-05 | 0.00293096 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331321 | AACCCGTGAACAAAA[C/T]TCCCAAGACCAGAGG | 51433 |
rs782519769 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336291 | TTTAAGAAAATTTTC[C/T]GAGTAAAAAATCCAT | 51433 |
rs782520252 | snp | C/T | 1.70348e-05 | 0.00291841 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345794 | TTGCACTTGAAATTA[C/T]ACTATTTCACAGGAA | 51433 |
rs782522470 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344747 | CCTGAGGTAGAAACT[A/G]ATTGGAGTAGTCAAG | 51433 |
rs782523287 | snp | C/T | 3.33661e-05 | 0.00408436 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337253 | AGTTGCCTTGTCATT[C/T]CTTTCCAACACAGCA | 51433 |
rs782528523 | snp | A/C | 1.67638e-05 | 0.0028951 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331439 | GTTGACTAATGACAG[A/C]CTAAACATTAATATC | 51433 |
rs782537629 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349193 | ACTAATTTAAGAAAT[C/T]AAACAGTTAGTAAAG | 51433 |
rs782538599 | snp | C/T | 1.73769e-05 | 0.00294757 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337441 | AAGGGTCAATAAACA[C/T]ATGAAAAGATATACT | 51433 |
rs782538891 | snp | C/T | 1.66098e-05 | 0.00288177 | missense | ANAPC5 | GRCh38.p7 | 12:121327227 | CCTGTTGCAGTGCCA[C/T]GGTGCTGGGTGGGGA | 51433 |
rs782540524 | snp | G/T | 1.64754e-05 | 0.00287009 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345908 | CTGGTCAGTTCCATA[G/T]CAGCATCCTCCACTG | 51433 |
rs782541033 | snp | C/G | 1.9525e-05 | 0.00312444 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352106 | TAAAAGTTTGCTGCA[C/G]GAGCAGGAGCCAGCG | 51433 |
rs782541218 | snp | C/T | 2.29972e-05 | 0.00339088 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346845 | ACATGACTTAGAAAG[C/T]TGCTCACTTCAATGA | 51433 |
rs782542772 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333568 | GTTGCAAAAATCATG[A/G]AGTTTTGAGGAGCCT | 51433 |
rs782544104 | snp | A/G | 1.69375e-05 | 0.00291006 | splice-donor-variant | ANAPC5 | GRCh38.p7 | 12:121335531 | AAGGTCTATAAACTT[A/G]CTAGTGACCGAAGCG | 51433 |
rs782548651 | in-del | -/T | 1.64781e-05 | 0.00287033 | frameshift-variant, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335604 | CCGGCCATAGCCCTC[-/T]TCCCCATTACTTTTG | 51433 |
rs782548790 | snp | C/G | 1.91507e-05 | 0.00309434 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347044 | TATTTTAGAAAGGCC[C/G]TTTGAATAATTTCTC | 51433 |
rs782549471 | snp | C/T | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354467 | TTTTGTTTTCTCAAT[C/T]GCTATTTGTTTAATG | 51433 |
rs782549649 | snp | A/G | 3.30759e-05 | 0.00406655 | intron-variant, synonymous-codon, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352236 | CAGCACCAGCACCGC[A/G]ATCTTGTACGGCGTC | 51433 |
rs782554549 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343977 | GTTTATTTGGAAGCA[A/G]TCTCAGATAACAGTA | 51433 |
rs782558078 | snp | A/C | 1.65734e-05 | 0.00287862 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345849 | ATTACCTTACAGATA[A/C]ATCAAGTTCTTCTTT | 51433 |
rs782565208 | snp | C/G | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352855 | CTGGGCTCGAGCGAT[C/G]CTCCCGCCTTCCCGA | 51433 |
rs782565936 | snp | C/T | 3.34762e-05 | 0.00409108 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331436 | CCTGTTGACTAATGA[C/T]AGACTAAACATTAAT | 51433 |
rs782567342 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325641 | GGAGGCTGAGGCAGG[C/T]GGATCACCTGAGGCC | 51433 |
rs782570189 | snp | C/T | 1.84773e-05 | 0.00303946 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352367 | ACTAAGTCTCGGGCC[C/T]GCGGCGCGCTGCCGC | 51433 |
rs782571963 | snp | C/G | 1.64846e-05 | 0.0028709 | missense | ANAPC5 | GRCh38.p7 | 12:121328393 | CAGGCTGTGTTTCCA[C/G]TGCAGGAGGTCGGAG | 51433 |
rs782572294 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349162 | TCCCAAAGTCTAGGC[A/C]CCAAGCCAAAAATTA | 51433 |
rs782574328 | snp | C/G | 1.87429e-05 | 0.00306123 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347040 | TGCATATTTTAGAAA[C/G]GCCCTTTGAATAATT | 51433 |
rs782576102 | in-del | -/A | 1.65905e-05 | 0.0028801 | frameshift-variant, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331408 | CTAATTGCCTCCTGC[-/A]GGGCGAGCTCTGCCT | 51433 |
rs782576230 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329508 | TTCCATTTTACTGAA[A/G]TCTGTCACAAACTTC | 51433 |
rs782576841 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338721 | ACTACCCAGAAATAA[C/T]GCTATTAATACTTTA | 51433 |
rs782577827 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340767 | GGGTTTCACCATGTT[C/G]GTCAGGCTGCTCTCA | 51433 |
rs782578968 | snp | C/T | 1.67063e-05 | 0.00289014 | synonymous-codon, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331347 | AGAGGATGGCCTCAC[C/T]AAACAGTGCTGGAGA | 51433 |
rs782580075 | snp | C/T | 1.65452e-05 | 0.00287616 | missense | ANAPC5 | GRCh38.p7 | 12:121327194 | CCTCCAGGCTGTTCA[C/T]GCTCAGCAACATCTG | 51433 |
rs782582390 | snp | A/G | 3.40142e-05 | 0.00412383 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337428 | CTCAGTAGAAAGAAA[A/G]GGTCAATAAACATAT | 51433 |
rs782583756 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327805 | AAATGTGAAAGTACA[A/C]AATAAGATGAAAATA | 51433 |
rs782584245 | snp | C/T | 1.66418e-05 | 0.00288455 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337288 | ATTCTGGGAAAGACT[C/T]ACCGCTTCAGCAAAA | 51433 |
rs782584534 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346343 | AACTGGCTCCCCCAA[A/C]CAGAGGTAATCTCCA | 51433 |
rs782585043 | snp | A/G | 1.65274e-05 | 0.00287462 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347904 | AAGGAGAGATAGGGA[A/G]GTATGGATTTTAAAG | 51433 |
rs782585262 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337443 | GGGTCAATAAACATA[C/T]GAAAAGATATACTAA | 51433 |
rs782587496 | snp | C/T | 3.33545e-05 | 0.00408364 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337255 | TTGCCTTGTCATTCC[C/T]TTCCAACACAGCAAC | 51433 |
rs782587988 | snp | A/C/G | 5.51205e-05 | 0.00524955 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352362 | CCGAGACTAAGTCTC[A/C/G]GGCCCGCGGCGCGCT | 51433 |
rs782589631 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328089 | GGAGATCACCCACCC[A/G]TTACCTCACAAAGTG | 51433 |
rs782589996 | snp | A/G | 1.68001e-05 | 0.00289823 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345824 | AAAGGATCCCTGTCA[A/G]AAAAGCCAAATTACC | 51433 |
rs782590227 | snp | A/C | 1.64762e-05 | 0.00287016 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345944 | TTCTCACCATTCTGG[A/C]AGTACTGCTGAAGGG | 51433 |
rs782594144 | snp | C/T | 6.87711e-05 | 0.00586351 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352127 | GGAGCCAGCGGGCGC[C/T]TCTCACCTGCAGCAG | 51433 |
rs782595703 | snp | G/T | 1.65181e-05 | 0.00287381 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330651 | TATCGGATCTCTTCT[G/T]CCCCAGCACATAAAG | 51433 |
rs782598255 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326570 | AGTCAACCAGGTTTC[C/G]GTTGGAGACCTGCCT | 51433 |
rs782600216 | snp | C/T | 3.35402e-05 | 0.00409499 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327260 | GGGAACAGGATTTCC[C/T]TTCAGCAGCAGACCT | 51433 |
rs782602157 | snp | C/T | 4.95618e-05 | 0.00497779 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352276 | TTGATGCCGAACACA[C/T]TGGCGTGCACAACCC | 51433 |
rs782604638 | snp | A/G | 3.29484e-05 | 0.00405871 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335631 | TTTGCTTTCGGCTCC[A/G]GTAAGAATCAGACGA | 51433 |
rs782607306 | snp | A/T | 3.38679e-05 | 0.00411495 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331459 | ACATTAATATCCCAT[A/T]AATAATCACAAACAT | 51433 |
rs782609377 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343936 | TATGAAATACATACA[C/T]ATCTTTTTGCCTGCA | 51433 |
rs782613584 | snp | A/G | 6.7555e-05 | 0.00581145 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331333 | AAACTCCCAAGACCA[A/G]AGGATGGCCTCACCA | 51433 |
rs782615086 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329400 | CTCACGATCCACCCG[C/T]CTTGGCCTCCCAAAG | 51433 |
rs782615694 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331843 | AATCACTTTTATGTT[A/T]GTTTGTTTGTTTTTT | 51433 |
rs782618623 | snp | A/C/T | 3.30438e-05 | 0.0040646 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345857 | ACAGATACATCAAGT[A/C/T]CTTCTTTTTCCATTT | 51433 |
rs782622147 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342586 | ATCGAGGAGGCCAAG[C/T]GCGGTGGCTCACACC | 51433 |
rs782624625 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349560 | GGGAGTGAGATCCCA[C/G]CACTCTAAAAAAATT | 51433 |
rs782625733 | snp | C/T | 2.18243e-05 | 0.00330328 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346867 | CTTCAATGAAAATAC[C/T]CTCTGCTCTTCTTAG | 51433 |
rs782626145 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329907 | GGTGTGAGCCACCAC[A/G]CCCAGCCAGATAAGC | 51433 |
rs782631974 | in-del | -/TT | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327765 | AATGCGGCAACAAAG[-/TT]TTTACTTCCAGGCTA | 51433 |
rs782633186 | snp | C/T | 1.6489e-05 | 0.00287128 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347798 | AGAAGAAAATGAAGT[C/T]TACCTGATCTGCACT | 51433 |
rs782635394 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336392 | GCCTCAAAACTGTCA[G/T]TTAGGCTGGGCGTGA | 51433 |
rs782636173 | snp | A/G | 1.68043e-05 | 0.0028986 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335538 | ATAAACTTACTAGTG[A/G]CCGAAGCGGCAGTGC | 51433 |
rs782637455 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346297 | TGGCTGTTACACTAT[C/T]TGAAATGATATTTAT | 51433 |
rs782639128 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344960 | AGGGGCTTCCCCAGA[C/T]GCTGCCTGAAGAACA | 51433 |
rs782639940 | snp | A/G | 3.35154e-05 | 0.00409348 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121327105 | GCCTACCTGCTCCGC[A/G]TGTAGCTCTGCGAGG | 51433 |
rs782644583 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327974 | GCCCGGTGCTTGGAG[C/T]CAGATGACGTGGGTT | 51433 |
rs782646633 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333637 | ATACCCTTAATAACA[A/T]CTTTGGTCTAGGCCT | 51433 |
rs782647462 | snp | A/T | 1.65056e-05 | 0.00287272 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330637 | CAGCAGAACATAGCT[A/T]TCGGATCTCTTCTGC | 51433 |
rs782652251 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345393 | TTAACAAAGGATCAA[C/T]TGACAAAAGTAGGGG | 51433 |
rs782652513 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338657 | GGGGAAAAATTATTC[C/G]AAAAATATAGAAAAC | 51433 |
rs782660104 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354489 | TGTTTAATGAATAAT[A/G]AATGAATATGCATTA | 51433 |
rs782665427 | snp | A/G | 9.29982e-05 | 0.00681839 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346886 | TGCTCTTCTTAGAAG[A/G]GTTTCATACCTACTA | 51433 |
rs782665869 | snp | A/G | 1.70122e-05 | 0.00291647 | intron-variant, missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121352153 | AGCAGGGGCAGGAGC[A/G]GCTGGTTGAGCCTCC | 51433 |
rs782666547 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346094 | GGCTACGCAATGGCA[A/G]CTCCACAATGGCAAT | 51433 |
rs782671501 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343983 | TTGGAAGCAATCTCA[A/G]ATAACAGTAGTTAGG | 51433 |
rs782672840 | snp | C/T | 1.69611e-05 | 0.00291209 | splice-donor-variant | ANAPC5 | GRCh38.p7 | 12:121327095 | CCGGCCACCTGCCTA[C/T]CTGCTCCGCGTGTAG | 51433 |
rs782674844 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351244 | TGGGCGTAGTGACCC[A/G]CGCCTGTACTCCCAG | 51433 |
rs782677197 | snp | A/G | 0.000151112 | 0.00869098 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331442 | GACTAATGACAGACT[A/G]AACATTAATATCCCA | 51433 |
rs782677803 | snp | C/T | 1.72633e-05 | 0.00293791 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331316 | AATTCAACCCGTGAA[C/T]AAAACTCCCAAGACC | 51433 |
rs782678299 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342364 | CATCCACATGCAAAA[C/G]CATGAAGGTGGATCC | 51433 |
rs782680330 | snp | A/G | 1.65004e-05 | 0.00287227 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121328447 | GTTTGCCGTCTTCCC[A/G]GCAAAAGCTCTCTGT | 51433 |
rs782684542 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346862 | GCTCACTTCAATGAA[A/G]ATACTCTCTGCTCTT | 51433 |
rs782689692 | snp | A/G | 8.32882e-05 | 0.00645269 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327238 | GCCATGGTGCTGGGT[A/G]GGGAGAGGGAACAGG | 51433 |
rs782691105 | snp | G/T | 1.66868e-05 | 0.00288845 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337246 | CAAAAAAAGTTGCCT[G/T]GTCATTCCTTTCCAA | 51433 |
rs782691156 | snp | A/C | 1.87577e-05 | 0.00306243 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352384 | CGGCGCGCTGCCGCC[A/C]GTTGTCACCACAAGG | 51433 |
rs782692427 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352121 | CGAGCAGGAGCCAGC[A/G]GGCGCCTCTCACCTG | 51433 |
rs782697365 | snp | A/T | 1.64827e-05 | 0.00287073 | utr-variant-5-prime, missense | ANAPC5 | GRCh38.p7 | 12:121347871 | AGTTTTGACAGTGTA[A/T]TATCTGGGCCCTGTG | 51433 |
rs782698170 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333148 | TGGTGAAATCCCATC[G/T]CTACTAAAAATACAA | 51433 |
rs782699007 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349017 | CGCCTGTAATACCAG[C/T]GCCTTGGGAGGCTGA | 51433 |
rs782699989 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341584 | GAAATGGTGGCTGAA[G/T]AGAGAGTGGTTAGAT | 51433 |
rs782700933 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338578 | TGGGTGACAGGGCAA[C/G]ACTCAGTCTCAAAAA | 51433 |
rs782703883 | in-del | -/C | 5.62308e-05 | 0.0053021 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352381 | CGCGGCGCGCTGCCG[-/C]CCAGTTGTCACCACA | 51433 |
rs782704382 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326007 | ACAAGCGAGAGACAG[A/G]CTTGCAACATTCCCA | 51433 |
rs782705163 | snp | A/G | 0.000134385 | 0.00819599 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346085 | TGACATCCAGGCTAC[A/G]CAATGGCAACTCCAC | 51433 |
rs782708433 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347128 | GATTTGTATAAAATG[A/G]TGGCTCATAAAACAA | 51433 |
rs782709603 | snp | C/T | 1.65343e-05 | 0.00287521 | missense | ANAPC5 | GRCh38.p7 | 12:121327170 | TCTGCTGCACGCCCG[C/T]ATTCACCGCCTCCAG | 51433 |
rs782710597 | snp | C/T | 3.35351e-05 | 0.00409468 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335540 | AAACTTACTAGTGAC[C/T]GAAGCGGCAGTGCAG | 51433 |
rs782711392 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324005 | AAAGAATTCACTCTA[C/T]CTCCTCTGGGTTGCA | 51433 |
rs782713280 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331258 | CTGAAGATCTCTGCT[C/G]CAACTGCAAAACAAC | 51433 |
rs782713877 | in-del | -/A | 1.65244e-05 | 0.00287436 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347781 | CACCTTTTCATATAT[-/A]AAGAAGAAAATGAAG | 51433 |
rs782720615 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329067 | GCGCTTACTTCAAGG[A/T]GCCACTTTTGTCATT | 51433 |
rs782722967 | snp | C/G/T | 8.25724e-05 | 0.006425 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347898 | TGTGTAAAGGAGAGA[C/G/T]AGGGAGGTATGGATT | 51433 |
rs782723850 | snp | C/T | 0.00123846 | 0.0248534 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352353 | CATGGCGGCCCGAGA[C/T]TAAGTCTCGGGCCCG | 51433 |
rs782730699 | snp | G/T | 1.69913e-05 | 0.00291468 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345807 | TATACTATTTCACAG[G/T]AAAAGGATCCCTGTC | 51433 |
rs782735823 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353855 | CCTCAGCCTCCAGTT[-/A]AAAGTAGGTAATTAG | 51433 |
rs782735998 | snp | A/G | | | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121342044 | GTTTTTGGGACAGAG[A/G]CCCACTGCAAGATAC | 51433 |
rs782737088 | snp | A/G | | | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345905 | CTACTGGTCAGTTCC[A/G]TATCAGCATCCTCCA | 51433 |
rs782739179 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334537 | ACCATTATTTACATT[A/G]TTTCATTATTTCCAA | 51433 |
rs782739674 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336991 | TTGGGAGGCCGACGC[A/G]GGCAGATCATGAGGT | 51433 |
rs782741112 | in-del | -/A | 1.67528e-05 | 0.00289415 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328279 | CTCCTGCTTCTCTCT[-/A]AAAGAATTCACACCC | 51433 |
rs782742660 | snp | A/G | 1.65605e-05 | 0.0028775 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328307 | CCCCCAGGGCCTTGG[A/G]AGACCTACCTGCGGC | 51433 |
rs782742735 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355501 | GGCAGAGGTTGTAGT[A/G]AGCCGAGGTCATGCC | 51433 |
rs782743805 | snp | A/C | 1.76225e-05 | 0.00296833 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335482 | AACAGCAGACTTTTT[A/C]TTGTCATCGGTTCCT | 51433 |
rs782744057 | snp | C/T | 4.12218e-05 | 0.00453974 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330742 | AGTGAAATATCAATG[C/T]GGTCATAAGAAAGAA | 51433 |
rs782745124 | snp | C/T | 1.648e-05 | 0.0028705 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335599 | AAGCTCCGGCCATAG[C/T]CCTCTTCCCCATTAC | 51433 |
rs782753405 | snp | A/G | 1.65993e-05 | 0.00288086 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330567 | GGAAACAATCTCACA[A/G]AAAGATGAGCCTTAC | 51433 |
rs782755157 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344582 | GTGAGACTTGATCTC[-/A]AAAAAAAAAAAAAAA | 51433 |
rs782755332 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327661 | ATACAAAAACAAGAC[G/T]GGTAAAAAAGGCACT | 51433 |
rs782763427 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330515 | CTGGTTAATGACAGA[-/G]GTGGGCAGAAAAAGA | 51433 |
rs782765400 | snp | A/G | 3.42924e-05 | 0.00414065 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342073 | ACCTCCTCTTCTCTG[A/G]AAAAAATAAAAAAAC | 51433 |
rs782769195 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331040 | ACAACATCTCACCCA[A/G]TTACTAAGTGTAGTA | 51433 |
rs782773565 | snp | A/G | 8.07722e-05 | 0.00635449 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330739 | TCTAGTGAAATATCA[A/G]TGTGGTCATAAGAAA | 51433 |
rs782774292 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331558 | TGTAACTATTTCTGG[A/G]CTTATTCTCTCAGAG | 51433 |
rs782776336 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341663 | TATGGGTAATTACCA[C/T]ACACTGCTTTTCAGG | 51433 |
rs782777339 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345880 | TTCCATTTTTCTTTC[A/G]CCCTCATCTCTACTG | 51433 |
rs782782474 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329193 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 51433 |
rs782785477 | snp | G/T | 1.85317e-05 | 0.00304393 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346057 | AGACGAGAGACAAGG[G/T]GAAAGCATTAACTGA | 51433 |
rs782788637 | snp | A/G | 1.87443e-05 | 0.00306134 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342111 | GTAAAGAATTACACA[A/G]AAGTAAAAATGATAA | 51433 |
rs782795244 | snp | C/G | 1.65935e-05 | 0.00288036 | missense, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331409 | TAATTGCCTCCTGCA[C/G]GGCGAGCTCTGCCTG | 51433 |
rs782795936 | snp | A/T | 4.98649e-05 | 0.00499299 | synonymous-codon, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331419 | CTGCAGGGCGAGCTC[A/T]GCCTGTTGACTAATG | 51433 |
rs782798597 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327395 | AACCTTGCCCTCAGG[A/G]TAAGAAAGGCAGAAA | 51433 |
rs782798768 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355789 | ACCTTGAGCCCAGGA[A/G]TTCAAGGCTGCAGTG | 51433 |
rs782799438 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338354 | CAGCACTTTGGGAGG[C/T]CGAGGAGGGCAGATC | 51433 |
rs782799456 | snp | A/C | 3.3095e-05 | 0.00406773 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346961 | GAAAGGTCATCAAAA[A/C]ACTGTTCCATATCCT | 51433 |
rs782800081 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337239 | AAACAAACAAAAAAA[G/T]TTGCCTTGTCATTCC | 51433 |
rs782801355 | snp | A/C/T | 0.00018352 | 0.00957749 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121337392 | TCTTTAGCAAAGAAG[A/C/T]CTGAAATTTAAAAAT | 51433 |
rs782801972 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324344 | AAGATGAAGAAAGGG[G/T]TAAAGGACTGACTTA | 51433 |
rs782801975 | snp | A/G | 3.51822e-05 | 0.00419402 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335491 | CTTTTTATTGTCATC[A/G]GTTCCTTCAATTTGC | 51433 |
rs782802352 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334355 | ACACAGAGAAAGGGA[C/T]AGATGTCTCCATTAT | 51433 |
rs782808071 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325422 | GAGCTGAGATCACAC[C/T]ATTGCACTCCAGCCT | 51433 |
rs782810221 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332962 | AGAACAACCTGGGCA[A/G]CATAGCAAAACCTTG | 51433 |
rs782819146 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335617 | TCTTCCCCATTACTT[C/T]TGCTTTCGGCTCCGG | 51433 |
rs796314109 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311319 | TAGAAAAATATTCCA[C/T]GCAAACAATAACCAA | 51433 |
rs796561423 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313052 | GAAAAGAGGCCGGGC[A/G]CGGTGGTTCACGCCT | 51433 |
rs796925548 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318208 | TTATCCTTTCAATAC[A/T]CAAACGTAGTCACAG | 51433 |
rs4545636 | snp | G/T | | | | | | : | TTTACACAGGGCCCA[G/T]ATATTACACTGTCAA | 51433 |
rs200117205 | snp | A/C | | | | | | : | GAGCTACACATTGTT[A/C]GTTTTTTTTTTTTTT | 51433 |
rs200994464 | snp | C/T | | | | | | : | CAAGTTTTTTTTTTT[C/T]TTTTTCACTGCTGTA | 51433 |