SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs144353263 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136980 | ATTTAAGAGTTTGTT[A/C]AAGACGTACATTTCA | 996 |
rs144370733 | snp | G/T | 0.00993419 | 0.0697739 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118673 | TTGAAGCAAACATTT[G/T]GCTTGATCAAAATGT | 996 |
rs144441744 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47187162 | TGCTGCTATGAAAAA[C/G]AAGCAAATTTGACAT | 996 |
rs144545702 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47180871 | ACTGTACATTTAAGT[G/T]ACAGGTTAGGATTTG | 996 |
rs144644006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138600 | TCTCTTCCTCTCTGA[A/G]TCCCTGACTAGAGAG | 996 |
rs144657691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135474 | GCATCAAATGAATAA[C/G]AAAAAAGCACAACAT | 996 |
rs144676189 | snp | C/T | 5.01836e-05 | 0.00500892 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171958 | AAGCAGGTATTTGCA[C/T]TGCGGTGTAGTACAA | 996 |
rs144762081 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137482 | GGAGGAGCTTCAGTA[-/G]GATACTCAATTCTAA | 996 |
rs144785568 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47151083 | CTATTTGTTTGACTC[C/T]AAAGTGAAATGTACA | 996 |
rs144880397 | snp | A/C/G/T | 0.0284327 | 0.115793 | intron-variant | CDC27 | GRCh38.p7 | 17:47137120 | CCAGCACCATCAATA[A/C/G/T]GACTTTGTCTTTGTA | 996 |
rs144985864 | snp | G/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157233 | TAAGACACTTACAAT[G/T]GTGTCCTGGGGTGTT | 996 |
rs144986630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47173583 | TAACTCCCAGTCACA[A/G]TAATGCTGTCTCAAT | 996 |
rs145069806 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CDC27 | GRCh38.p7 | 17:47141346 | CTTTAGGTTAATCAT[C/T]CTCTCCTTTTCTGGT | 996 |
rs145171680 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47148753 | ATATAAGCCAAAAAA[C/G]CAGTAAAGCAACATC | 996 |
rs145199949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159230 | CCGGGTCCTCTGTAC[A/G]GAGACTCTAGTGTGG | 996 |
rs145325689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47126415 | GTCTACTGTGGCTCA[C/G]GGGGCTGCCTGATAT | 996 |
rs145379298 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47157617 | CAAGAACACTAATTT[G/T]AAACATAACAAATCG | 996 |
rs145390571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179087 | TTATATCATTCTGCT[C/G]TTCCTTCTTTCTGAT | 996 |
rs145466111 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CDC27 | GRCh38.p7 | 17:47160466 | CCTGGACTCAAGTGA[C/T]CCACCCGCTTCAGCC | 996 |
rs145632553 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | CDC27 | GRCh38.p7 | 17:47176315 | TGTTCAGAGTCATTT[C/G]TACTGTTGAACATTT | 996 |
rs145709830 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CDC27 | GRCh38.p7 | 17:47134503 | TTGTTTTGTTTTGTT[C/T]TGTTTTTGAGATGGA | 996 |
rs145802800 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47182713 | TAAATAATATTTCCA[C/T]TGTATAAACATATCA | 996 |
rs145846012 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131935 | CTCGGCCTCCTAAAG[C/T]GCTGGCATTACAGGC | 996 |
rs145847421 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140602 | TCTTTAATTAAATAT[G/T]TGGGTCACCACTATA | 996 |
rs145925799 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CDC27 | GRCh38.p7 | 17:47128742 | TAATGCACACACATT[C/T]GTTTTCTTTTTCTGT | 996 |
rs145945685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47124018 | AAAGTTTTGACCAAG[C/T]GTTTTTACTTATTTG | 996 |
rs145956947 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136866 | AGCAACAAAGTAACA[A/C]AACTAAACAAACAAA | 996 |
rs146003838 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150768 | CCAGGCACGGTGGCT[A/C]ATGCCTGTAATCCCA | 996 |
rs146006352 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137107 | AAATTAGTAAGTACC[A/G]GCACCATCAATACGA | 996 |
rs146040423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47177167 | AGTAGGGCGCAGCAG[C/T]ACATGCCTGTATTCC | 996 |
rs146057722 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47138092 | AGGTGTGAGCCACCA[C/T]ACCCAGCAGCATTCT | 996 |
rs146143202 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CDC27 | GRCh38.p7 | 17:47147929 | AAAAAGGCTGGGCGC[A/G]GTGGCTCACACCTGT | 996 |
rs146208684 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47146344 | CCAGAACCTACAACT[C/G]GGCAGTTCAGACAGT | 996 |
rs146301864 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47169790 | ATTTTAATAAGGTCA[C/T]AGAATCAGACTATGT | 996 |
rs146307308 | in-del | -/ACAC/ACACAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124178 | TCTAGTACACTGAAA[-/ACAC/ACACAC]ACACACACACACACA | 996 |
rs146444727 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | CDC27 | GRCh38.p7 | 17:47161057 | TTAGATCAAAAATTT[A/C]TTTCTTTTTTTTTTT | 996 |
rs146484354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47135309 | GCTATGTAATAGTGT[A/G]TTAGGTTAATATGCA | 996 |
rs146488360 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47132505 | TGGTGGTCTTAGAGG[A/G]GAGGCAAAAAATACC | 996 |
rs146488361 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47165771 | TTTTCTAAAAGTTTA[A/C]TAGTTTTATGTTTTA | 996 |
rs146569035 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47183494 | TTTGGGATCTCCAGA[A/G]CCTCTTGTTTAACCT | 996 |
rs146584045 | snp | A/G | 0.000126687 | 0.00795784 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181608 | CGCATCTCGGTAAGC[A/G]TAGTGGTTTAGTGCT | 996 |
rs146808547 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47145128 | ATTCTCCCATTTCAG[A/G]TAACTACAAACTGAA | 996 |
rs146850848 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CDC27 | GRCh38.p7 | 17:47148279 | TAAAAAAACAAAACA[A/G]AACAAAAAACCCAAC | 996 |
rs146889026 | snp | C/T | 0.00438332 | 0.0466095 | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117325 | TCAGCTGACATTAAA[C/T]GGCAGGTCCTAGGGA | 996 |
rs146936699 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47166804 | CTTTCATTCAGTTCA[A/G]TATATTTTTAAAATC | 996 |
rs146997390 | snp | C/T | 1.66161e-05 | 0.00288232 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138802 | AAGAGCAACATCTTT[C/T]TGAAGATGCCAAAGT | 996 |
rs147022277 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47153194 | TGACACTGCATGCAG[A/T]CCTACATGCGTGACT | 996 |
rs147156754 | snp | A/C | 0.00270619 | 0.0366847 | intron-variant | CDC27 | GRCh38.p7 | 17:47181526 | TTCATATATGTTATT[A/C]ATTTATCATTCTACA | 996 |
rs147192717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47186482 | TAATTGCTAAATCTA[C/T]ATAAAATCTCTTTGC | 996 |
rs147282427 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47134104 | AGGTCTCACTATGTT[A/G]ACCAAGCTGGTTTCA | 996 |
rs147298194 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132780 | ATTATTATTATTATT[A/T]TATTTTAAAGATAGC | 996 |
rs147305442 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CDC27 | GRCh38.p7 | 17:47135967 | AACATGGTGAAATCC[C/T]GTCTCTACTAAAAAT | 996 |
rs147346652 | snp | A/T | 4.54969e-05 | 0.00476932 | intron-variant | CDC27 | GRCh38.p7 | 17:47137364 | AGCACACCAGGCCTT[A/T]AAAAAATGGGAACAA | 996 |
rs147410397 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47146771 | TCCAGTAATCAACAA[C/T]GTAAAATTTATAGCC | 996 |
rs147507965 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47133884 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCATGTGT | 996 |
rs147511271 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47163669 | TTAACTGCATCTTTA[A/G]AAAAACTTTAATGAT | 996 |
rs147511356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47130233 | GGGCGTGGTGTCACA[C/T]GCCTGTAGTCCGAGC | 996 |
rs147557114 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CDC27 | GRCh38.p7 | 17:47178943 | GGGTGGCTGGGATTA[C/T]AGGCATGTGCCACTA | 996 |
rs147617501 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157336 | AGACAGTTGCTAAAG[C/T]TCTGTAAAGATGTGA | 996 |
rs147666773 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47131586 | AGAACTTAAGGTACC[A/G]TACTTACACAGAAGC | 996 |
rs147669982 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47126550 | CTATCACTATATATA[C/T]CATAGTCCAGACAAC | 996 |
rs147721623 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137122 | AGCACCATCAATACG[A/G]CTTTGTCTTTGTACT | 996 |
rs147769898 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47139907 | GTTTGAGGATTTAGG[C/T]TATATAAAATCAGTT | 996 |
rs147815063 | snp | A/C | 0.00199809 | 0.0315445 | splice-donor-variant | CDC27 | GRCh38.p7 | 17:47158204 | CAACCCCACCCACCT[A/C]CCTATTTCACATAAT | 996 |
rs147873995 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131966 | ATGAGCCACTGCAAC[C/T]GGCCAGGAGATATCT | 996 |
rs147890925 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131960 | ACAGGCATGAGCCAC[C/T]GCAACTGGCCAGGAG | 996 |
rs148044751 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47149811 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCACA | 996 |
rs148087250 | snp | A/C | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137267 | TATAGGCATAAGCGT[A/C]ATTTGGATCAACTTG | 996 |
rs148098429 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47146001 | TCAATCATGTGGCCA[A/G]TGATTCCATCAATCA | 996 |
rs148216483 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178810 | CTCTTTCCTTTTTCC[-/G]TTTTTTTTTTGAGAC | 996 |
rs148257449 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CDC27 | GRCh38.p7 | 17:47121548 | GCTCAAGTGGTATGA[C/T]TCTCCTGCCTCAGCC | 996 |
rs148329804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168711 | TGCTTACTCATGTTC[G/T]CAAGAGTGGTGTTAA | 996 |
rs148410755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47188101 | TTAAAATATTTACTG[C/T]TTGATACCTCAAGCC | 996 |
rs148462470 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47181027 | GAGGCCAAGGCAGGT[A/G]GATCACCTAAGCTCA | 996 |
rs148470613 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47134623 | TGGGACTACAGGCAC[C/G]CATCACCACACCCAG | 996 |
rs148497428 | snp | A/C/T | 0.000828038 | 0.0203309 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157383 | AGGATCTGGCTTTTC[A/C/T]CCTGTGAAGACAAAA | 996 |
rs148510863 | snp | A/C/T | 3.34517e-05 | 0.00408961 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171961 | CAGGTATTTGCATTG[A/C/T]GGTGTAGTACAACTG | 996 |
rs148551974 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131964 | GCATGAGCCACTGCA[A/C]CTGGCCAGGAGATAT | 996 |
rs148566591 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47151720 | TTATTCTAGAATCCA[C/T]GAGAGTCACTATCTG | 996 |
rs148688644 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47159253 | TAGTGTGGGTCTTGA[C/T]GAGGTGGTCAGTGAA | 996 |
rs148694711 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47177241 | GCATGGGCAACATAG[A/G]GAGATCTTGACTTAA | 996 |
rs148731873 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47135968 | ACATGGTGAAATCCC[A/G]TCTCTACTAAAAATA | 996 |
rs148851448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47173468 | TAAGTTAGAAAGTTT[G/T]ATTTCCTCTAGATTT | 996 |
rs148886367 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47127361 | AAAGGAATTACTAGA[A/T]AAATTATATATTTAA | 996 |
rs148892033 | in-del | -/AGGAA/AGGACAGGAA | 0.510425 | 0.0508886 | intron-variant | CDC27 | GRCh38.p7 | 17:47174990 | AGGACAGGACAGGAC[-/AGGAA/AGGACAGGAA]AGGAAAGGAAAGGAG | 996 |
rs148956369 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145282 | GAAAAGAAAATGTTG[A/G]GAATTTGAGAAAGCC | 996 |
rs149056353 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47165823 | TGAGTTAAATTTTTA[A/G]TAAGGTATGGGGTTT | 996 |
rs149076670 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47153222 | ACTTTTCTGGGAATG[G/T]CTTGTAATAAGGTAA | 996 |
rs149146701 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47149248 | AGGTGCGGTGGGGCT[C/T]ATGACTGTAATCCCA | 996 |
rs149217282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47162097 | TTTCTTTCTGTGTGT[A/G]TTTTAAGGACACCAC | 996 |
rs149282669 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CDC27 | GRCh38.p7 | 17:47187106 | TTCACCTAGTCATAT[C/T]CTAAAACTTTCTACC | 996 |
rs149334649 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47180715 | GGTGTTTATTAAGCA[C/T]TGATTACCAAGCCAG | 996 |
rs149379098 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CDC27 | GRCh38.p7 | 17:47175966 | CTATGACTTAGGGCA[A/G]AGTTACTTAACTTCT | 996 |
rs149474782 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157319 | TTGTGCAAGAGTTGG[A/G]CAGACAGTTGCTAAA | 996 |
rs149486294 | snp | A/C | 0.191147 | 0.242974 | intron-variant | CDC27 | GRCh38.p7 | 17:47147153 | CGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 996 |
rs149583496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47167986 | TCACAAAGGATACAG[A/C]TGAAGAGTGCATAGG | 996 |
rs149591730 | snp | A/G | | | splice-donor-variant, intron-variant | CDC27 | GRCh38.p7 | 17:47171915 | AATATTTTAAAACTT[A/G]CTTGCTGAGATCAAC | 996 |
rs149606787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155623 | TGTATTTATACATAC[A/C]TATACTTCTAATAAT | 996 |
rs149742046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164859 | AAACTAAACCACAGA[A/G]CTTATTTGAATTTTA | 996 |
rs149757322 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | CDC27 | GRCh38.p7 | 17:47165683 | ATAAAATTTATCAAC[-/T]TTTTATTTTATGTAC | 996 |
rs149765071 | snp | G/T | 0.00915221 | 0.067025 | intron-variant | CDC27 | GRCh38.p7 | 17:47134480 | TGCCTAATTGTTTTT[G/T]TTTTGTTTTGTTTTG | 996 |
rs149805671 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191109 | AATAGAAGCTGTGAG[A/G]TCCCTTAGGCCTAGG | 996 |
rs149826276 | in-del | -/TTATTATTATTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132742 | AGCCATTAAAGCAGT[-/TTATTATTATTA]TTATTATTATTATTA | 996 |
rs149846983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140499 | TTCAAAGTTTTCAGA[A/G]TCTGTTGCTTCCTCT | 996 |
rs149864837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47182147 | ACAGAGATATTAAAA[C/T]GTATGTCATCCTCCC | 996 |
rs150022690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148683 | AGAGAAAAGACATAT[C/T]ACTACATATAGAGGA | 996 |
rs150076661 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47161863 | TTTCTTCTTGTAGTT[C/T]CTAAGTAAAGCCATT | 996 |
rs150116111 | snp | A/C/G | 3.3975e-05 | 0.00412148 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154691 | TTTGAAGGGGCTCCG[A/C/G]TGGATGGCACATCAA | 996 |
rs150179985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47126777 | AAACGGGCTTATTAG[A/G]TTTAAAATAAGCTTT | 996 |
rs150229852 | snp | A/G | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119115 | TTTGCCAATTAAAAA[A/G]ATAAAAGAATCTAAA | 996 |
rs150250105 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47175331 | GCCTTTCTAAAATGG[A/G]CCAATTTTGACAAAT | 996 |
rs150337028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132148 | AATAGGCTCCAGAAT[A/G]CTGTTTCAACACAAA | 996 |
rs150384989 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CDC27 | GRCh38.p7 | 17:47185478 | GTGAGGCACCGCGCC[C/T]GGCCTGTAATCATTA | 996 |
rs150409033 | snp | A/C | 3.45101e-05 | 0.00415378 | intron-variant | CDC27 | GRCh38.p7 | 17:47142040 | TCTAGGAGAAAACAA[A/C]ATAGTAAACAAAGGA | 996 |
rs150451511 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47152745 | ATCAGATATTAAAAC[-/C]TTATTTTAGCCTTTC | 996 |
rs150459989 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47137429 | AACCAAATCTATGAC[C/T]AAAATCAAGCCTCAA | 996 |
rs150561636 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137492 | CAGTAGATACTCAAT[C/T]CTAATTATTCACAGA | 996 |
rs150602555 | in-del | -/GGG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168169 | AAACCATTGGCTGTT[-/GGG]GGTGATAATCTTATC | 996 |
rs150700044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47129307 | CAGATCAAAATTAAA[C/T]AAATAACTTTCAGTT | 996 |
rs150753357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47122687 | ATACTTATTTATTTA[C/T]TTTTGAGATGGAGTC | 996 |
rs150771216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136967 | TTATCATTAGTTAAT[G/T]TAAGAGTTTGTTAAA | 996 |
rs150774271 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47177428 | CTAAAAATACAAAAA[C/T]TAGGTGGGCGTGGCC | 996 |
rs150913248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155436 | ATTTTAGTAGAGATA[C/G]GGTTTCACCATGTTG | 996 |
rs151002779 | snp | C/T | 8.39116e-05 | 0.00647679 | intron-variant | CDC27 | GRCh38.p7 | 17:47157211 | TAATATTTTGAACAC[C/T]AGAATATAAGACACT | 996 |
rs151053521 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CDC27 | GRCh38.p7 | 17:47152332 | AAAAAATAATAATAC[A/G]ATAAGATTTTATACT | 996 |
rs151090024 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118699 | AATGTGTTCTTCTTC[A/G]GGTTGTTTGATCCCC | 996 |
rs151137179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166437 | TCCTTTCACTGTCCT[C/T]AGGGTAGGTAGTGAT | 996 |
rs151160074 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CDC27 | GRCh38.p7 | 17:47135498 | ACAACATATCTGCTT[C/T]ATTTGAGTGGCTTTA | 996 |
rs151273354 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147432 | AACAAACAAACAAAA[-/C]AAAAAAACACTAGGC | 996 |
rs151311385 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47179349 | ACCAAGAAAACTGTT[A/G]CCAAGAATTCTGAGG | 996 |
rs180772914 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190449 | CAGATGAGGAAACAG[G/T]TTTTGAAAGTTACTT | 996 |
rs180777711 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47169082 | CAGCAGCTCCAACCT[C/T]CTGGGCTCAAGAGAT | 996 |
rs180781315 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179412 | TAGTGATGCCTACTA[C/T]GGTTGCAAATCAGAG | 996 |
rs180800345 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126520 | AAACAATCAAAGAAA[A/T]CCCCACAAAAATGGC | 996 |
rs180804636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47144362 | TTGAACTAAAAATAA[A/T]CCTCATAAAACTCTG | 996 |
rs180834032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135597 | AAAACAAAAGAAAGG[C/T]TATCTATTTTGTACT | 996 |
rs180842772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47141401 | ATTTAATTAAAATCC[A/G]AAGAGTAAAAAGCCT | 996 |
rs180855598 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165096 | AACTTCTGAAATTGG[C/T]TTTTTTCACTTGCCA | 996 |
rs180877710 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47159330 | GGGGTCAGGTAGTTG[A/C/T]AGGTCTTAGAGATGG | 996 |
rs180917098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47185020 | AATCTGACTGATTAA[G/T]GGGTTAGTCCCCAGG | 996 |
rs180934339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47123441 | TCTGAGACAGAATCT[C/T]GTTCTCTTGCCCAGG | 996 |
rs180955998 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47152609 | TATGACTATTGTATC[A/G]GTGCACTGTTTTTCC | 996 |
rs180985776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47130506 | AAAAGATTTAAAAAG[C/T]ACCAAACCTCACTAT | 996 |
rs181120186 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47174958 | AACTCGGTCGAAACA[A/G]GACTATCGAAACAGG | 996 |
rs181127507 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47154602 | GATTTTCCCTGAGAT[A/T]ACCTTTAAAAGATTG | 996 |
rs181293032 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47122812 | CTGAGTAGCTCGGAC[A/T]ACAGGTGCCCACCAC | 996 |
rs181414358 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47164804 | CCTGAGCGACAGAGC[A/G]CAAGATTCCATTTCA | 996 |
rs181418695 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132828 | AGGCTGGAGTGCAGT[A/G]GCTCAATCACGGCTC | 996 |
rs181535327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174712 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA | 996 |
rs181561220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184227 | TTATTGGAGTTGTTT[G/T]GTGGATTAAATGAAA | 996 |
rs181574577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47131936 | TCGGCCTCCTAAAGC[A/G]CTGGCATTACAGGCA | 996 |
rs181578061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47153310 | TGTGCCTGCCCACTG[C/T]CTTAACTTGCTCTGG | 996 |
rs181601953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158972 | GCCCAGGCAGGTCTC[C/G]AACTCATGAGCTCAA | 996 |
rs181613738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148082 | ACATGCCTGTAATCC[C/T]AGCTACTCAGGAGGC | 996 |
rs181658554 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47170363 | CCACCACACCCAGCT[A/C]ATTTTTAATTTTTTT | 996 |
rs181671161 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47178847 | TCGCTCTGTTGCCCA[A/G]GCTGGAGTGCAGTGG | 996 |
rs181845173 | snp | A/G | 1.67251e-05 | 0.00289176 | missense, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151932 | GACTGTAAAACACGA[A/G]AAGTCTAAGGTTTGT | 996 |
rs182009077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134624 | GGGACTACAGGCACG[C/T]ATCACCACACCCAGC | 996 |
rs182018838 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47158366 | TGTATCATAAACTTT[C/T]AGTATAAAAAATTAG | 996 |
rs182073580 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47134979 | TACATGTGTGCCAAG[A/G]CCATTGCTAAATTAT | 996 |
rs182180178 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119889 | AATCTGAAGCAGAGA[A/G]TCAAAAAGAATGGAA | 996 |
rs182245823 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47126985 | TTTCAGTAGAGACAG[G/T]GTTTCACCATGTTGG | 996 |
rs182285668 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47128250 | TGGCCAGGCTGGTCT[C/G]GAACTTCTGACCTCA | 996 |
rs182287651 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47169604 | GAACTGAGATCACAC[A/C]ATTGCACTCCAGCCT | 996 |
rs182288360 | snp | C/T | 0.00861728 | 0.0650721 | intron-variant | CDC27 | GRCh38.p7 | 17:47172111 | GTTCAGTATATTGAA[C/T]GATAATCAGTTTATC | 996 |
rs182289393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47137046 | ATGTACCATCCCTAA[A/G]TATAAGTAACCAAAT | 996 |
rs182296265 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47149032 | TGCAGGGAGCCAAGA[G/T]TGTGCCATTGCACTC | 996 |
rs182333352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124603 | GATTTATTTTTTAAC[A/G]AAAAATAACTATATA | 996 |
rs182337313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143205 | CTAAGCTCAAGTGAT[C/T]GGCCCACCTTGGCCT | 996 |
rs182366358 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47176479 | GTATTTTAAAACCAC[A/C/G]CTTAGAGTAAAAAGA | 996 |
rs182419868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47187340 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 996 |
rs182425317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47167687 | CATCAATACAGAAGA[A/C]TTCTGTGACCAAATG | 996 |
rs182486825 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47137767 | CACTTTTAAGTAGGA[C/T]GGCTTCAGGCAAGTC | 996 |
rs182531663 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47147738 | CTCTACAAAAAAATA[A/C]AAAATAAAAATAATC | 996 |
rs182545445 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47124439 | CAGGCATGCGCCACC[A/G]CACCCAGCTAATTTT | 996 |
rs182554120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47142724 | TTTAAAAGTAAGAAA[A/G]TAAGTAGATGTAATT | 996 |
rs182604402 | snp | A/C | 0.000883759 | 0.0210023 | intron-variant | CDC27 | GRCh38.p7 | 17:47154641 | AAGTTGCTTTAATCA[A/C]TTCCCAAACTGCATT | 996 |
rs182754912 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47160975 | TGGACAAAGTAGGAA[A/G]CAGAAGTAGGATGCA | 996 |
rs182796760 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47166864 | ATTATTTATTTATTT[A/T]ATTTTTTTGAGATGG | 996 |
rs182797028 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47133381 | GACCTCAGGTGATCC[A/G]CCCGCCTTGGCCTCC | 996 |
rs182807211 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47155049 | AGAAATAAAGAAGAG[C/T]AGCTTTATAAATCTA | 996 |
rs182869263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176041 | CCTTTAAAGGTTGCT[A/G]TTAGGATTAAATGAC | 996 |
rs182876060 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133066 | ACACATACATATACA[C/T]ACACACACACACACA | 996 |
rs182908145 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175498 | ACCTATGGAACTTTT[C/T]ATGATTTGTGACACA | 996 |
rs183047531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127495 | GCAACCTCTGCCTTC[C/T]AGTTTCAAGCGATTC | 996 |
rs183078406 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47186578 | CACTTAGGCTAGTGT[C/G]TCTTTCCAAATAGTT | 996 |
rs183086580 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47180599 | AGTACATAACCCAAG[A/G]AAATGACTCAAAAAA | 996 |
rs183107417 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47136164 | AAACAAACAAACAAA[A/C]AAAAAACTGAGTTCT | 996 |
rs183165362 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135730 | TTTGATATGGTTAAG[G/T]TTTTTAAGAATGCAA | 996 |
rs183327589 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156366 | GATGGTCTCGATCTC[C/T]TGACCTCGTGATCTG | 996 |
rs183415078 | snp | G/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118065 | GACACAAAATTACAT[G/T]GTTTCAATGCAAACA | 996 |
rs183421855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141651 | CTATAAACCTATTCC[A/G]AGAAGTTGCAAAGAA | 996 |
rs183428277 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47186241 | CCAATGCACATTAAA[A/T]CTAAATTTCTCATTG | 996 |
rs183461305 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119338 | CCTAAAGACCCTGAC[C/T]TGAATTAATTTATAA | 996 |
rs183480758 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47160418 | TTTAGTAGAGATAGG[G/T]TTTCACCAGGTTGGC | 996 |
rs183586491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174085 | GGTGACAGAGTGAGA[G/T]TCTGTTTAAATAAAT | 996 |
rs183641768 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124180 | CTAGTACACTGAAAA[C/T]ACACACACACACACA | 996 |
rs183650342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172739 | TTCTTAATGCAAGTG[A/G]CATTTTTCACCCTTA | 996 |
rs183675905 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47166009 | CCACAAGTGGAATTA[C/T]TGGCTCAAATAGTAA | 996 |
rs183708682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136700 | ACTAAGTTCTTAATA[G/T]TAACTCAATAAACCA | 996 |
rs183712558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47129616 | ACATAATCAAATTAT[C/T]AGAGATAAGGTTGTA | 996 |
rs183799686 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191208 | GTCTACTTCTTAATG[G/T]GAAGAGTGGCAAAGT | 996 |
rs183807198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47144302 | CGTTACTACAAAATA[C/G]TAAAGATTATAGCAT | 996 |
rs183810492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47181372 | TATAAACCTGAATCA[A/G]TTCTACATAGTTATT | 996 |
rs183878164 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47168745 | ATAAACATACCACCG[A/T]TACACCTGAAAACGG | 996 |
rs183890937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47125934 | TATGTTTTCTTTCTA[C/T]GATTGCATATTATAA | 996 |
rs183934049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47150085 | TATTACAGCCATCCC[G/T]CCCATAAAGACTAAG | 996 |
rs184399527 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47130316 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 996 |
rs184453501 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47173489 | CTCTAGATTTTACAA[C/T]GGTCTGGTTTCTTTT | 996 |
rs184474699 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47151002 | ACACCACTGCACTCC[A/T]GCTTGGGCAACAAGA | 996 |
rs184479823 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47134792 | ATTGTTTTCTTTTTT[C/T]TTTTTTTTTTTTGTT | 996 |
rs184521617 | snp | A/C | 1.69726e-05 | 0.00291308 | intron-variant | CDC27 | GRCh38.p7 | 17:47157403 | TGAAGACAAAAAAAA[A/C]AAAAGTTTGTCTCTG | 996 |
rs184602383 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47177634 | TTTAAGATAAAACAG[G/T]AGACCTTAAGCAATT | 996 |
rs184631652 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47133940 | ATTTTTAGTAGAGAC[A/G]AGGTTTCCCCATGTT | 996 |
rs184642725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134057 | CCCCCAGCCTTCTTA[C/T]ATTAACATATTTTTA | 996 |
rs184724718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47162887 | ATACACATATGGATA[C/G]ATATATGTATAAATC | 996 |
rs184782835 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156054 | TTCATGAGGCTCACC[A/G]CTATCCATTAATGCA | 996 |
rs184794510 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47121628 | TAAAAATTTGTTTAG[A/C]GACAGGGTCTCACTG | 996 |
rs184794863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47183434 | AAAAGTAGTAAATGA[C/G]TTAGCCCTTTCTATT | 996 |
rs184805890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138427 | TTTATTTTAATTTAA[A/G]ATTATTAATTTTTTC | 996 |
rs184955378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47178142 | TCTCAACTCACTAGT[A/G]GACTGTGATGTCAAT | 996 |
rs184963221 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47158383 | GTATAAAAAATTAGG[G/T]AAAAGTTACAGAAGT | 996 |
rs185097402 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47143741 | TAACTTCACAAAAAT[C/T]ATAGATGGCCCTCTA | 996 |
rs185126384 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47188577 | GCACTGAGGCTTGGA[A/G]TTGTCTTCTCAAACC | 996 |
rs185175938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135880 | GGGTATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 996 |
rs185200438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124835 | ATTATTGTAAAAATA[C/G]CTTTGACCTCTAGGA | 996 |
rs185249853 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47168367 | AAAAAGATATCACTT[C/T]GGAGTTTCTAAGTGT | 996 |
rs185254861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47145574 | ATGAAGTAACTCCTA[A/G]ATACTTTCTGGATGG | 996 |
rs185259037 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117820 | TAGATAAACATTGCT[C/G/T]TAGTTTTTTGTGAAA | 996 |
rs185330758 | snp | C/T | 3.32762e-05 | 0.00407885 | synonymous-codon, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122586 | GAGGTGCGTTTGACC[C/T]AACTTCTTGTAAACC | 996 |
rs185350357 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47164408 | AATTTTAGACTTACA[C/G/T]AGAACTTGCAAAAAC | 996 |
rs185392970 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47183654 | TTGTAATACTTCCCA[C/T]TGCTATAATTCTGTA | 996 |
rs185429810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174298 | TTACTGGATAGGATT[A/G]ACAAAGATTTCATCT | 996 |
rs185459815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47139051 | AATTCAGCAATCTAC[C/T]ATGGCAGGTCAAATA | 996 |
rs185525802 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47140584 | AAGTTGAAACAGAGG[A/C]TTTCTTTAATTAAAT | 996 |
rs185533965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164926 | ATTTACAAATTTCTA[C/T]AACCACTACTACAAT | 996 |
rs185541144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127613 | TCACCAAGTTGGCCG[A/G]GCTGGCCTCAAACTC | 996 |
rs185551633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148239 | AAACCAAATCAATCT[A/G]GAGATGAAAGACAAA | 996 |
rs186094904 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47141508 | TGTCAAAAATTCACC[C/T]CAGTAATTAACTCTG | 996 |
rs186103048 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165303 | CACCTTACATTCCCA[A/C]CAGCAGTGTACGAGG | 996 |
rs186129379 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47126803 | GCTTTATGAAAAAAA[A/T]TTTTTTTTGAGACAG | 996 |
rs186172641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134981 | CATGTGTGCCAAGAC[C/T]ATTGCTAAATTATCT | 996 |
rs186208870 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47185238 | GGCTGGAGTGCAGTG[C/G]CGCGATCTCGGCTCA | 996 |
rs186214185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178961 | GCATGTGCCACTACA[C/T]CGGCTAATTTTGTAT | 996 |
rs186256637 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47180913 | TAGAGTCTAAATCCA[C/T]GTTCTTCACCATAGA | 996 |
rs186269182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179612 | TACAGTAAGAAATCA[A/G]TAAGTGATAGAATTA | 996 |
rs186278072 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47132165 | TGTTTCAACACAAAA[A/G]AGGACCAATTTTTAT | 996 |
rs186282931 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47174813 | ATACAAAAATCAGCC[A/G]GGTGTGGTGGCGTGC | 996 |
rs186283814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47154326 | CAGACATAATTTCTG[C/T]TATTTATAGTCAAGT | 996 |
rs186331400 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47158982 | GTCTCGAACTCATGA[A/G]CTCAAGTGATCTGCC | 996 |
rs186347643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136218 | TATCGGAAGAGACAG[C/T]AGCATTGGCAAGTTG | 996 |
rs186375548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184244 | TGGATTAAATGAAAT[G/T]ATCCATTTATAATGC | 996 |
rs186396982 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136696 | GTACACTAAGTTCTT[A/C]ATAGTAACTCAATAA | 996 |
rs186447343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47154615 | ATTACCTTTAAAAGA[C/T]TGAAATAAACAAGTT | 996 |
rs186452221 | snp | C/T | 0.231356 | 0.249304 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154677 | TGGAAAATACCTTTT[C/T]TGAAGGGGCTCCGGT | 996 |
rs186608264 | snp | C/G/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151834 | CAGAACTTTGTGTTT[C/G/T]TGCAAGAATTGGAGT | 996 |
rs186626416 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133002 | GCATATATATATATA[C/T]ATATATATATATATA | 996 |
rs186663950 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155284 | AGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 996 |
rs186899383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166342 | AGTTTTGGTAGTGTG[G/T]CTTATTAAGAAATTG | 996 |
rs186919326 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47173567 | CTCCCACAAACTAAT[G/T]TAACTCCCAGTCACA | 996 |
rs186921791 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120794 | TGTATACAGTCAGGG[C/T]CCAATGAAAGTGGCA | 996 |
rs186930073 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138099 | AGCCACCACACCCAG[A/C]AGCATTCTCTCTTTT | 996 |
rs186936423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47161238 | GCTATGTTGCCCAGG[C/T]TGGTCTCAAACCTGG | 996 |
rs186950159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172330 | TCTGTAAATATTTAA[A/G]AAAAGCATACACACA | 996 |
rs186989015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47130071 | ATTTATTTGAAAAAT[G/T]ATTTTACTGGCCAGG | 996 |
rs187007538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47151331 | TTTTAGAAAGGAGAA[A/G]GAAAATTGTATCTTC | 996 |
rs187081544 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47142156 | ATGAAGGTACTGTAA[C/T]GAACATAAAGAAATT | 996 |
rs187146180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47186412 | ATTAAATTAATTTTC[A/G]AAAGGCTTATTTACA | 996 |
rs187208573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124019 | AAGTTTTGACCAAGC[A/G]TTTTTACTTATTTGA | 996 |
rs187252449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124531 | TCAAGTAATCTGCCC[A/G]CCTCAGCCTACCAAA | 996 |
rs187255909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47142794 | AGCGATTCTCCTGCT[G/T]CAGCCTCCCGCGTAA | 996 |
rs187259209 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CDC27 | GRCh38.p7 | 17:47166978 | TCGTGCCTCAGACTC[C/T]CAAGTAGCTGAGATT | 996 |
rs187272126 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CDC27 | GRCh38.p7 | 17:47147815 | CTAACGCAAGAGAAT[C/T]GCTTGAGCCAAGGAG | 996 |
rs187418928 | snp | C/T | 0.000564576 | 0.0167919 | intron-variant | CDC27 | GRCh38.p7 | 17:47170075 | AAAGATTTTTAAAAA[C/T]CAATATAAAAAGCAG | 996 |
rs187462446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127183 | GGGTACAAGGAATTC[A/G]GCCTAGGAATTTGAG | 996 |
rs187483701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47133543 | CTCCCAGGTTCAAGC[A/G]TTTCTCCTGCCTCAG | 996 |
rs187488034 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47155255 | TAGCATATATGTATA[C/T]ATTTTTTTGAGACAG | 996 |
rs187497741 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176240 | TTCATCAACTTTTTT[C/T]TTTTCTGTTTTCAAT | 996 |
rs187573625 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47133299 | ATGCACCATCACGCC[C/T]GGCTAATTTTGTATT | 996 |
rs187695107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128320 | ACAGGTGTGAGCCAC[A/T]GCGCCCAGCCCTGAA | 996 |
rs187721374 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182540 | CATTTGTACATATCA[C/T]CTCTAAGCAGTATAA | 996 |
rs187747232 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137050 | ACCATCCCTAAGTAT[A/T]AGTAACCAAATTCAT | 996 |
rs187807226 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187946 | AGACAGGTAAATTTC[A/G]TAAGATATAATCTTA | 996 |
rs187813720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168007 | AGTGCATAGGGCGAG[G/T]CATGGGGAAAGAGAG | 996 |
rs187824241 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119005 | CTTCAGCAAGTTATG[C/T]TCTAAGCTTAGCTTT | 996 |
rs187942016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47136725 | AAACCAGAACACTGT[C/T]AAAAAGCAGCAACTA | 996 |
rs187955769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184691 | TGCCATCTCGAGAAT[A/C]TCACATACTGCTTCC | 996 |
rs187991581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47149540 | AAAAAAGAAATGTTA[A/G]AAAGAAGTCCTTCAA | 996 |
rs187998130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156232 | CAACCTCTGTCTCCC[G/T]GGTTCAAGTGATTCT | 996 |
rs188021170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47123255 | GTTATATCAACTCTT[C/T]ACAACTGTCCACAGT | 996 |
rs188033399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47140700 | TTAAATGGCTTTTCC[A/G]AACACAGCTCTTGCC | 996 |
rs188042602 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165077 | ATATAAATGGAATTA[C/T]AGAAACTTCTGAAAT | 996 |
rs188215062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168607 | ATCTCAAAGTTTCTT[C/G]ACTAAATGACAAGAA | 996 |
rs188219399 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119476 | CAGCTTGACTAACAA[A/T]TACAGGTAAGTTTGT | 996 |
rs188233175 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160659 | AAATGGAAAAAAATT[A/C]AGAACAGCAATTCTT | 996 |
rs188257538 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156561 | CAAGCAATTCTCCTG[C/T]CTCAGCCTCCTGAGT | 996 |
rs188270375 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47133998 | TTAAGTGATCTGCTT[A/G]TCCCAGCCTACCAAA | 996 |
rs188336773 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176583 | AGGAGAAAAAAGATG[A/G]CCAAATTGTGCAGGG | 996 |
rs188493350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47188957 | GGGTGAAGTAATGTA[C/G]GGCCAGAGGTAACAC | 996 |
rs188569226 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CDC27 | GRCh38.p7 | 17:47126049 | CACATAGCATCAGAG[C/T]TCTTACTTTTACCTT | 996 |
rs188577370 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47144352 | AATTCTTAATTTGAA[A/C]TAAAAATAATCCTCA | 996 |
rs188603524 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47168962 | GAAGCATTCCCATGG[C/G]CAGAGTTACTTGTTC | 996 |
rs188692008 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190313 | AGGATTAAGAGAATT[C/T]GATGTATTATAAATG | 996 |
rs188709921 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175859 | ATCTGTTAAGTTTTT[A/T]AATCAACTATAAGTA | 996 |
rs188780826 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47150511 | AACACCTGGGGTTAT[C/G]AGAAGCTGGAGGAGG | 996 |
rs188889322 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47178301 | AGCACTTTGGGAGAC[A/G]GAGGTGGGAGGACTG | 996 |
rs188940173 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47134963 | TTTACTGAGTAGTTA[C/T]TACATGTGTGCCAAG | 996 |
rs188950565 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47158686 | TGCAGTGGCATGATC[G/T]TGGCTCACTGCAACC | 996 |
rs188999729 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47174157 | GAGCAATCTGAAGTG[G/T]TGTGACACGGGTGGT | 996 |
rs189019339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47124649 | AAAAAGTTATTGAGA[A/G]GAGTGGCATTAACAT | 996 |
rs189028638 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47130403 | GAAAAAAAAGAAAAA[G/T]GATTTTACTGTTTTA | 996 |
rs189142664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47173113 | GAGAACCACTGTTGT[A/G]AAGTACAAGACAAAC | 996 |
rs189150646 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47129738 | AGTTCAACTGCTTCA[C/T]TAAAGATGAGAATAC | 996 |
rs189321943 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47152271 | ACTAAAAAATTTTAA[C/G]ACAGCTAAATTCTCA | 996 |
rs189458289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134258 | AATCAAATCAAATCA[A/G]ACTATGATAATAAGG | 996 |
rs189464692 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157968 | CTAGAGGACACCAGA[C/T]ACTTGAAAATAGATT | 996 |
rs189473236 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47139165 | TTCTACCAAAAAGAC[C/T]GAAGAGAAATCTATA | 996 |
rs189484779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138539 | AATGAAATAGCTGCT[C/T]TGTGATTTTTCTATT | 996 |
rs189495010 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164262 | TTGTGCATATGCACT[C/T]TATGATGTTCACAAA | 996 |
rs189500954 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47131596 | GTACCGTACTTACAC[A/G]GAAGCTAATAAATGC | 996 |
rs189526491 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CDC27 | GRCh38.p7 | 17:47183605 | AGATTAGGCACCATT[A/G]TTATACACTCTAATT | 996 |
rs189552691 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47183970 | GATAAATAGAAGAAT[C/T]ATTTTATTATGCAAA | 996 |
rs189715352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47186992 | ATTTGCAGCACTATC[C/T]CTGATCATTGATCTT | 996 |
rs189749140 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CDC27 | GRCh38.p7 | 17:47159167 | TCCAGGCTTAATTCA[C/T]TTTATTTTTCTTGTG | 996 |
rs189755094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47164535 | CAAAACTGTAAACTA[C/T]GCTGGACACGGTGGC | 996 |
rs189837608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47122777 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCTTCAG | 996 |
rs189979653 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47178994 | TTTAGTAGAGATGGG[G/T]TTTCTCCATGTTGGT | 996 |
rs190095345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47144124 | TGATCAGTTCTTTTC[A/G]TGGTTTCTCTATGAA | 996 |
rs190133624 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47125103 | TTTGTATTTTTAGTA[G/T]AGATGGGGTTTCACT | 996 |
rs190164295 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47132575 | TTTTAAATAAAAAAA[A/T]TTTTTTTTGAATTAG | 996 |
rs190169844 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47154578 | GGCAAAAGCAATTAC[A/G]TAAAGTAAGATTTTC | 996 |
rs190213189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174847 | TGTGATCCCAGCTAC[A/T]CGGGAGGCTGAGGCA | 996 |
rs190297549 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CDC27 | GRCh38.p7 | 17:47147443 | CAAAAAAAAAAACAC[G/T]AGGCATAGAAAACAG | 996 |
rs190319543 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47160414 | ATATTTTAGTAGAGA[C/T]AGGGTTTCACCAGGT | 996 |
rs190362959 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47171658 | AAGAAAACGAAATAT[C/T]TGTGATCATTTAAGA | 996 |
rs190374473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47181054 | CTCAGGAATTTGAGA[A/C]CAGCCTGGGCAACAT | 996 |
rs190379445 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47177882 | CACACACACACACAT[A/C]TCTCCAAAGAGCTAT | 996 |
rs190393361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47121808 | GCAATGGCGTGATTT[C/T]GGCTCACTGCAACTT | 996 |
rs190408349 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47127976 | CCTCCAAAGTGACGG[A/G]ATTATAGGGATTTTT | 996 |
rs190417159 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47148854 | GGAGGCCAAGATGGG[C/G]GATCACCTGAGGTCA | 996 |
rs190431885 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47153157 | GTACACTGCACTCAA[A/T]ACCTGGTTTGATATT | 996 |
rs190521918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47127316 | TAAAAATAGAAACCC[A/G]TGTCTTCATAAAGAA | 996 |
rs190542640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47126920 | TGCCTCAGCCACTTG[A/G]GTAGCTGGGATTACA | 996 |
rs190670322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175474 | GTTGTGTGAATTTAA[A/G]GGCATAGAACCTATG | 996 |
rs190706891 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134509 | TGTTTTGTTTTGTTT[C/T]TGAGATGGAGTCTCA | 996 |
rs190731720 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156249 | GTTCAAGTGATTCTC[C/T]TGCCTCAGCCTCCCG | 996 |
rs190781834 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47174478 | ACCATCCTTTATTTA[C/T]AGACTTAATTAAAAT | 996 |
rs190819495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47135920 | CCAAAGTGGGTGGAT[A/C]ATGAGGTCAGGAGAT | 996 |
rs190829506 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47159576 | CCCAGTAGCCTCTGC[A/G]CACGGGGACAATCGA | 996 |
rs190832816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47149774 | AGCCTGGCCAACATC[A/G]TGAAACCCTGTCTCT | 996 |
rs190840742 | snp | C/T | 2.81821e-05 | 0.0037537 | intron-variant | CDC27 | GRCh38.p7 | 17:47154621 | TTTAAAAGATTGAAA[C/T]AAACAAGTTGCTTTA | 996 |
rs190846076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47179800 | GTACATAAATAACGT[A/G]GATTAAACAGCTTTA | 996 |
rs191009767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47185644 | TTGGCTCAAGTGATC[C/T]GTCTGCCTCAGCCTC | 996 |
rs191054875 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165353 | CTCTCACCAGCACTT[A/G]GTATTGTCAGTAGTT | 996 |
rs191062942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47133300 | TGCACCATCACGCCC[A/G]GCTAATTTTGTATTT | 996 |
rs191068147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172584 | TATATTTAAGATAAA[C/T]TATAAATTGTGAATG | 996 |
rs191069814 | snp | A/G | 0.00633908 | 0.0559406 | intron-variant | CDC27 | GRCh38.p7 | 17:47154809 | GAGGTTGAAATCAAG[A/G]TGTCAAAAAGTCATC | 996 |
rs191120547 | snp | C/T | 2.86217e-05 | 0.00378286 | intron-variant | CDC27 | GRCh38.p7 | 17:47142197 | AAGTACATAATAAAA[C/T]ACAAAGATAATATTA | 996 |
rs191238420 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CDC27 | GRCh38.p7 | 17:47124564 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 996 |
rs191246523 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142838 | CATGAGCCACCACGC[C/T]CGGTTAATTTTTATT | 996 |
rs191299996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47167609 | ATGTGATAATAAAAA[C/T]GAACTTTGAGTGTGG | 996 |
rs191352596 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47124424 | GCGTAACTGGGATTA[A/C]AGGCATGCGCCACCA | 996 |
rs191372464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166399 | CATGTGCATAGAGTT[C/G]TTTTAAGTTTTCAGC | 996 |
rs191391386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47136237 | ATTGGCAAGTTGATT[A/G]TTACATTGGTCAGCA | 996 |
rs191442983 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47182857 | GATTCATCTCCTGGG[G/T]TATATATTTAAGAAT | 996 |
rs191480947 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47170187 | CTTCCTTCCTTCATC[C/T]CTCCCTCTCTCTGTC | 996 |
rs191491981 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47138198 | CTGTTTCAAACTCTC[C/T]ATCACTCCCAGGAAC | 996 |
rs191502067 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47161913 | TCTTTAGAAAATCTC[C/T]GTCTGGTGAGAATCC | 996 |
rs191623781 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47186552 | AATATTCAAAAAGCT[C/T]TCACTGAAGTCACTT | 996 |
rs191727743 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47147983 | AGGTGGGCGGATCAC[A/G]AGTCAGGAGTTTGAG | 996 |
rs191785273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47130222 | AAAAATTAGCCGGGC[A/G]TGGTGTCACACGCCT | 996 |
rs191797923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47151339 | AGGAGAAAGAAAATT[G/T]TATCTTCCTTTTAAA | 996 |
rs191862447 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173914 | CCTGGCCAACATGGC[A/G]AAACCCCGTCTTCTA | 996 |
rs191913185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47150940 | AGGAAGCTGAGGCAG[A/G]AGAATCACTTGAACC | 996 |
rs192088631 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CDC27 | GRCh38.p7 | 17:47124079 | TAAATCTTAATCAAT[A/G]TACTTCCTTATTGTA | 996 |
rs192093051 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47183649 | TTCCTTTGTAATACT[C/T]CCCACTGCTATAATT | 996 |
rs192122410 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CDC27 | GRCh38.p7 | 17:47176421 | TTTCAATACCAACTG[A/G]TTTTATACCTGTTGT | 996 |
rs192149415 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133906 | GGCATGTGTCACCAC[A/G]CCCAGCTAATTTTCT | 996 |
rs192167120 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47125926 | AGAATTGATATGTTT[C/T]CTTTCTATGATTGCA | 996 |
rs192170318 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47134023 | ACCAAAGTGCCGGGA[A/C/T]TGCAGGTGTGAGCTA | 996 |
rs192265983 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47176594 | GATGGCCAAATTGTG[C/T]AGGGCTTTGTAAACT | 996 |
rs192410899 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47175911 | ACCGACTCTGAAGCT[A/T]GACTGCTTGGGTTCA | 996 |
rs192468303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47141650 | TCTATAAACCTATTC[C/T]GAGAAGTTGCAAAGA | 996 |
rs192566247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156302 | TGCCACCACACCCGG[A/C]TAGTTTTTTGTATTT | 996 |
rs192667062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47178040 | CAGGTATTGGTGGTG[A/G]GAAAGAAAAATACAT | 996 |
rs192684254 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47188384 | ACAGCACTGTGCGTC[A/G]AAGCATACCCTGGTG | 996 |
rs192792234 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119697 | TTATCATTTTATATG[A/C]ATAATTGAATTCTTA | 996 |
rs192802443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47160826 | GGTACCCTTGGGGAA[C/T]CAGATATTAGTTTGC | 996 |
rs192833478 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47173463 | TTACATAAGTTAGAA[A/G]GTTTGATTTCCTCTA | 996 |
rs192904204 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189880 | TAAGGGAAAAGCAGT[A/G]TAACAGAGAACGCTA | 996 |
rs192941971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47144196 | GCTTCTCAGCTTGCA[A/G]ATGGCCTCTTGTGGG | 996 |
rs193006158 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47137514 | ATTCACAGATTCCAT[A/C]TTTGTGAATTTGTCT | 996 |
rs193008947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47182226 | ACTCCAGGAAGCATA[C/T]TGGAATGCAAATGAG | 996 |
rs193030816 | snp | A/T | 6.59239e-05 | 0.00574087 | synonymous-codon, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122547 | AGGATCTAAATCCAT[A/T]GCCCAAGAGAAATTC | 996 |
rs193061947 | snp | A/G | 0.499717 | 0.0118838 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157051 | ATTACAGCTGAATCA[A/G]TATAAGACACTGAGG | 996 |
rs193087627 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164349 | CATGACTGTATAACA[C/T]ATTTGTGATTTTAAC | 996 |
rs193150560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168172 | ACCATTGGCTGTTGG[C/T]GATAATCTTATCACC | 996 |
rs193151027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124706 | CAGCTAGATTCTCAC[A/G]TCTATCTGCTTCTCC | 996 |
rs193157511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168710 | TTGCTTACTCATGTT[C/T]GCAAGAGTGGTGTTA | 996 |
rs193302633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143608 | CTAATAATCACTGAT[C/T]TGTTGTCCATTCCTA | 996 |
rs199529489 | snp | A/C | 0.00157638 | 0.0280305 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169967 | AGCTGAATCACCAAA[A/C]TCAGTAACAATATCA | 996 |
rs199536674 | in-del | -/GTT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132779 | ATTATTATTATTATT[-/GTT]ATATTTTAAAGATAG | 996 |
rs199551316 | in-del | -/AT | | | frameshift-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138879 | TTCTAACCTCTGAGA[-/AT]ATTCTTTCAGCCTGA | 996 |
rs199585923 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136664 | AAAGTAAAATAGAGA[G/T]ACTGCTAAATAAAAG | 996 |
rs199588106 | snp | C/G | 0.00143427 | 0.026741 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137360 | CTGCAGCACACCAGG[C/G]CTTAAAAAAATGGGA | 996 |
rs199588648 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136964 | CTATTATCATTAGTT[A/C]ATTTAAGAGTTTGTT | 996 |
rs199588670 | snp | G/T | 0.0456505 | 0.144018 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156934 | GTTAATGGACTAAGA[G/T]CTGCTGGTCCTCCTA | 996 |
rs199609959 | in-del | -/CCACTTACCAT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137144 | CTTTGTACTTCATTA[-/CCACTTACCAT]GCATTATAATGTCTA | 996 |
rs199626169 | snp | A/C | 0.000568847 | 0.0168553 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138794 | AGAACTGAAAGAGCA[A/C]CATCTTTTTGAAGAT | 996 |
rs199660984 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135560 | AAAGGTATTAAACAC[G/T]ATGCTAATGATAGTG | 996 |
rs199678268 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132144 | GTGTAATAGGCTCCA[A/G]AATACTGTTTCAACA | 996 |
rs199702746 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147346 | GGAGCTTGCAGTGAG[C/T]CGAGATCGCGCCACT | 996 |
rs199711781 | snp | A/T | 0.0625051 | 0.165365 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154709 | GATGGCACATCAATT[A/T]CAGGAGGTGTATTAG | 996 |
rs199718821 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135669 | GCATTTAAACTCCTC[C/T]TAGTAAAAGCTTGCC | 996 |
rs199734317 | snp | C/T | 0.00115278 | 0.0239804 | intron-variant | CDC27 | GRCh38.p7 | 17:47129348 | AAGGGATAACGTTGT[C/T]TTTAAGCAATACAAC | 996 |
rs199743911 | snp | G/T | 0.00498757 | 0.0496881 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143921 | TAAAGAGTCGTGAAC[G/T]TCTTCGAGGCAGTGC | 996 |
rs199746290 | snp | A/T | 0.000225712 | 0.010621 | intron-variant | CDC27 | GRCh38.p7 | 17:47143871 | TGTGACATACAGAAA[A/T]CTTTAAATTACCTTG | 996 |
rs199754068 | snp | C/T | 0.00199798 | 0.0315436 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142284 | TGTGATTGTGGATAT[C/T]TTCCCTTCTGAAATG | 996 |
rs199771997 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174604 | ATCAATCGTGTACTA[A/G]TTAAATTATGCTATG | 996 |
rs199779693 | snp | G/T | | | synonymous-codon, missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141976 | GCAGTTGTATGAACA[G/T]AAAGCTAAATAACCT | 996 |
rs199782161 | snp | C/G | 0.021577 | 0.101602 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47170035 | AGATTTGTTCCCCTT[C/G]TGCAAGCCTTTAAAA | 996 |
rs199786640 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142956 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 996 |
rs199808134 | snp | A/C/T | 0.000148583 | 0.00861808 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132320 | CGCTTTTTGGAAATG[A/C/T]ATTTCTGCAAGGCTG | 996 |
rs199828413 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160405 | TAATTTTTATATTTT[-/G]AGTAGAGATAGGGTT | 996 |
rs199829285 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141787 | GCCTTCTTAAGCATG[A/G]GCATTTATTTTAATG | 996 |
rs199829880 | snp | A/C/G | 0.000272992 | 0.0116803 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189215 | GTGCCTCAGGCCCCC[A/C/G]CTGTAGCGGCTCCGG | 996 |
rs199831009 | in-del | -/AAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133286 | GGGATTACAGGCATG[-/AAC]CACCATCACGCCCGG | 996 |
rs199862699 | in-del | -/AGT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134297 | ACCACACCCCTAAAC[-/AGT]CCATATAGATTTTTT | 996 |
rs199867550 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156614 | ACCATGCCCAGCTAA[-/C]TTTTTGTATTTTTAG | 996 |
rs199871618 | in-del | -/GCTCCTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184258 | TGATCCATTTATAAT[-/GCTCCTA]GTATACTATCATACA | 996 |
rs199890121 | snp | C/T | 4.95913e-05 | 0.00497928 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151891 | AGAAGACAGACTTTG[C/T]TCCAGTTTGGCCGAT | 996 |
rs199899451 | snp | A/T | | | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157355 | GTAAAGATGTGAATT[A/T]AAATGTTTGGTCAGG | 996 |
rs199907013 | snp | A/G/T | 0.0315097 | 0.121501 | stop-gained, synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171994 | TCCTTTCAAGAGTCT[A/G/T]TATGCTTTATATGCC | 996 |
rs199907808 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158899 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 996 |
rs199927167 | snp | G/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138882 | TAACCTCTGAGAATA[G/T]TCTTTCAGCCTGAAA | 996 |
rs199929234 | in-del | -/T | 0.107341 | 0.205301 | intron-variant | CDC27 | GRCh38.p7 | 17:47126802 | GCTTTATGAAAAAAA[-/T]TTTTTTTTTGAGACA | 996 |
rs199939780 | in-del | -/CCG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133988 | CTCCTGGCCTTAAGT[-/CCG]GATCTGCTTGTCCCA | 996 |
rs199958545 | in-del | -/AAG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174937 | TCCAGCCTGGGCAAC[-/AAG]AGCGAAACTCGGTCG | 996 |
rs199984087 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130128 | GCACGTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 996 |
rs200005516 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139415 | GGGACTACAGGCGCC[C/T]GCCACCACACCTGGC | 996 |
rs200013071 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161488 | AGGCACGGTGGCTCA[A/T]GCCTGTAATCTCAGC | 996 |
rs200040594 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134509 | GTTTTGTTTTGTTTT[-/C]TGAGATGGAGTCTCA | 996 |
rs200044815 | in-del | -/ACTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174600 | AGAAATCAATCGTGT[-/ACTA]GTTAAATTATGCTAT | 996 |
rs200045428 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187426 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 996 |
rs200049256 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150798 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 996 |
rs200061079 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154727 | GGAGGTGTATTAGTG[C/T]AGTTTTGTAAATAGG | 996 |
rs200099646 | snp | C/G/T | 0.00572081 | 0.0531784 | intron-variant | CDC27 | GRCh38.p7 | 17:47137102 | AAGAAAAATTAGTAA[C/G/T]TACCAGCACCATCAA | 996 |
rs200109000 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185306 | GCCTCAGCCTCCTGA[G/T]TAGCTGGGACTACAG | 996 |
rs200113063 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160289 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 996 |
rs200138369 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168995 | TTTCTTTTTTTTTTT[C/T]TTTTTTTTTTTTTGG | 996 |
rs200148088 | snp | C/T | 0.000103822 | 0.00720417 | intron-variant | CDC27 | GRCh38.p7 | 17:47156886 | TTTGGTATTATAGCA[C/T]ATTTGAAAGTATCTT | 996 |
rs200148949 | snp | A/T | 0.00912975 | 0.0669442 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157001 | GTTTAGATAATATGG[A/T]AGTTCCTGTTCCCAG | 996 |
rs200174584 | snp | C/T | 0.000252634 | 0.0112362 | intron-variant | CDC27 | GRCh38.p7 | 17:47122418 | GTAACTTTCTAAATA[C/T]TCAAAATCATATGTA | 996 |
rs200176916 | snp | A/C | 0.00199806 | 0.0315442 | intron-variant | CDC27 | GRCh38.p7 | 17:47158200 | CTCTCAACCCCACCC[A/C]CCTACCTATTTCACA | 996 |
rs200177060 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136527 | GAAAAATACAATAAA[C/T]GTCAACAGTAAGTAT | 996 |
rs200184818 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139361 | AAGCTCCGCCTCCCG[A/G]GTTCACGCCCTTCTC | 996 |
rs200189475 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142404 | GTTTGGGATTTTAGG[C/T]GGAAACTTCATTTTT | 996 |
rs200200993 | snp | C/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137270 | AGGCATAAGCGTAAT[C/T]TGGATCAACTTGGAT | 996 |
rs200208345 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128964 | TTTTAGTAGAGATGG[A/G]GTTTCACCATGTGGC | 996 |
rs200208812 | snp | C/T | 0.00020724 | 0.0101773 | intron-variant | CDC27 | GRCh38.p7 | 17:47123981 | AAAGGCAAAGAAAAA[C/T]CTTAAAGTAGCAAAA | 996 |
rs200216131 | in-del | -/AT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142183 | ATTTACTTAAAATAA[-/AT]GTACATAATAAAATA | 996 |
rs200218137 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161522 | TTGGGAGGCCAAGGC[A/C]GGTGGATCACTTGAG | 996 |
rs200224683 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161857 | TTTTTTTTTCTTCTT[A/C]TAGTTCCTAAGTAAA | 996 |
rs200226011 | snp | C/T | 0.00199802 | 0.0315439 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142286 | TGATTGTGGATATTT[C/T]CCCTTCTGAAATGAT | 996 |
rs200232067 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135664 | CGTCAGCATTTAAAC[C/T]CCTCCTAGTAAAAGC | 996 |
rs200233075 | in-del | -/AAGGAAGT | 0.370974 | 0.218781 | intron-variant | CDC27 | GRCh38.p7 | 17:47175091 | AGGAAGGAAGGAAGG[-/AAGGAAGT]AAGTTGTAGCAGCAC | 996 |
rs200248769 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133827 | AATCTCAGCTCACTG[C/G]AACCTCTGCCTCCTG | 996 |
rs200250209 | in-del | -/AC/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147430 | CAAACAAACAAACAA[-/AC/C]AAAAAAAAACACTAG | 996 |
rs200268612 | snp | C/T | 0.0148893 | 0.0849881 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154689 | TTTTTGAAGGGGCTC[C/T]GGTGGATGGCACATC | 996 |
rs200272570 | in-del | -/CC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135511 | TTATTTGAGTGGCTT[-/CC]TATATATCATTATAC | 996 |
rs200288937 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131877 | GGTCTCGCTATGTTG[-/C]CCAGGCTGGTCTCCA | 996 |
rs200291606 | in-del | -/GAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159997 | CTGCTGAAACCTCTG[-/GAC]CTTCTTTTTTTTTTT | 996 |
rs200305810 | in-del | -/AC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136313 | CTACTGCAAAATGAG[-/AC]ATAATCCATTAACAA | 996 |
rs200308794 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130189 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 996 |
rs200309713 | in-del | -/AGCACCTGGT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160515 | ACAGGCGTGAGCCAC[-/AGCACCTGGT]CGCCTCCTCCTTAGC | 996 |
rs200313358 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174605 | TCAATCGTGTACTAG[A/T]TAAATTATGCTATGT | 996 |
rs200323430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47142928 | TGATCTGCCTGCCTT[A/G]GCCTCCCAAAGTGCT | 996 |
rs200329637 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142959 | GGGATTACAGGCATG[A/G]GCCACCGTGCCCGGC | 996 |
rs200340309 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157231 | TATAAGACACTTACA[A/G]TTGTGTCCTGGGGTG | 996 |
rs200340830 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135712 | CCTCCTTTAAACACA[G/T]TTTTTGATATGGTTA | 996 |
rs200367374 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161728 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 996 |
rs200389111 | snp | C/T | 0.00212983 | 0.0325635 | intron-variant | CDC27 | GRCh38.p7 | 17:47137408 | TTAAAATTTTACTTT[C/T]TCTAAAACCAAATCT | 996 |
rs200397153 | in-del | -/AGAAACC | 0.104149 | 0.203046 | intron-variant | CDC27 | GRCh38.p7 | 17:47171670 | ATTTGTGATCATTTA[-/AGAAACC]AGAAACCAATAAGAA | 996 |
rs200443406 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142764 | CCGCAACCCAACCTC[C/T]GCCTCCCGGGTTCAA | 996 |
rs200454606 | in-del | -/T | 0.0225045 | 0.103662 | intron-variant | CDC27 | GRCh38.p7 | 17:47185187 | CTATAAATTTTTCTC[-/T]TTTTTTTTTGAGACA | 996 |
rs200456245 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136894 | AAAAAACAACTACAG[C/T]ATCTGCAAAAGTTTG | 996 |
rs200469306 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | CDC27 | GRCh38.p7 | 17:47136163 | AAACAAACAAACAAA[-/C]AAAAAAACTGAGTTC | 996 |
rs200483082 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142341 | CAGGCTATCATTTAT[A/G]TTAGGTTGAGTTATT | 996 |
rs200529536 | snp | G/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151858 | TTGGAGTTACCTCTC[G/T]GCTATTTCCACTCTG | 996 |
rs200543265 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132390 | CTGAAAGTATAAAAC[A/G]AAGTATAATTTTAAA | 996 |
rs200565458 | snp | C/T | 0.0168555 | 0.0902421 | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47138892 | GAATATTCTTTCAGC[C/T]TGAAATAAAAAAAAC | 996 |
rs200576636 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173944 | ACTAAAAATACAAAA[-/A]TTAGCCAGGCGCGGT | 996 |
rs200577228 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175795 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 996 |
rs200590868 | snp | G/T | 0.000247392 | 0.0111191 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129480 | AATGGCTTTGTTTAG[G/T]GTATCCAAAGCCTTC | 996 |
rs200592731 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158203 | TCAACCCCACCCACC[C/T]ACCTATTTCACATAA | 996 |
rs200611688 | snp | C/G | 0.498978 | 0.0225869 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156937 | AATGGACTAAGAGCT[C/G]CTGGTCCTCCTAATA | 996 |
rs200626406 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148075 | CAGTGGCACATGCCT[A/G]TAATCCCAGCTACTC | 996 |
rs200673051 | in-del | -/ACA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184280 | TATACTATCATACAT[-/ACA]TAAGCACTTGGAAAA | 996 |
rs200676775 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143930 | GTGAACTTCTTCGAG[C/T]CAGTGCGTTTGGGGG | 996 |
rs200697385 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151811 | TGATAAATACCTTGT[C/T]TGTGGACCAGAACTT | 996 |
rs200707548 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177858 | TTTATATGTGTGTGT[A/G]CACACACACACACAC | 996 |
rs200717000 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136580 | CAAACTTTTTCATAT[C/G]TTATTCAGTTGATAA | 996 |
rs200720095 | in-del | -/CATGCATTAT | | | frameshift-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137152 | TTCATTACCACTTAC[-/CATGCATTAT]AATGTCTAGGATTGA | 996 |
rs200732402 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147323 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 996 |
rs200758374 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168996 | TTCTTTTTTTTTTTC[C/T]TTTTTTTTTTTTGGA | 996 |
rs200764837 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | CDC27 | GRCh38.p7 | 17:47133438 | CCAAGCTGTTTTTTT[-/T]GTTTTTTTTTTGAGA | 996 |
rs200768419 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47152532 | TTGCTTGGCTCTTCA[A/G]TCTTCTCTAATTTAT | 996 |
rs200776434 | in-del | -/AC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134064 | CTTCTTATATTAACA[-/AC]TATTTTTAATTTTTT | 996 |
rs200785494 | in-del | -/AG | 0.0283406 | 0.115616 | intron-variant | CDC27 | GRCh38.p7 | 17:47175029 | GAAAGAAAGAGAGAA[-/AG]AGAGAGAGAGAGGAA | 996 |
rs200816984 | in-del | -/CA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133085 | ACACACACACACACA[-/CA]AACACACACACACAA | 996 |
rs200820305 | in-del | -/TG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140261 | GGGACCACAGGTGAG[-/TG]CCACCACACCCAGCT | 996 |
rs200828523 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147388 | TGGGCGACAGAGCGA[A/G]ACTCCGTCTCAAAAA | 996 |
rs200834582 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151887 | TGTGAGAAGACAGAC[G/T]TTGTTCCAGTTTGGC | 996 |
rs200836601 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151841 | TTGTGTTTGTGCAAG[A/G]ATTGGAGTTACCTCT | 996 |
rs200857474 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143135 | TACCATCCCAGCTAA[-/T]TTTTTTTTTTCAGAG | 996 |
rs200888347 | in-del | -/AG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169230 | CCTGGCCTCAAGTGA[-/AG]TCCTCCCACCTCCAC | 996 |
rs200895472 | snp | C/T | 0.00034562 | 0.0131412 | intron-variant | CDC27 | GRCh38.p7 | 17:47123873 | TGTTTGGGACCATGA[C/T]CCCAGTCTTTACCTT | 996 |
rs200907637 | snp | C/G | 0.00639799 | 0.0561966 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137332 | TGTTCCCGTTGCAGA[C/G]TGAAACAGTTCCCTG | 996 |
rs200923883 | in-del | -/TGATCT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155308 | TGGAGTGCAGTGGCA[-/TGATCT]CAGCTCACTGCAACC | 996 |
rs200940073 | snp | A/G | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141881 | GAAAGTTCAAAATAG[A/G]CCCTTCCAATTTGGC | 996 |
rs200957941 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139371 | TCCCGAGTTCACGCC[A/C]TTCTCCTGCCTCAGC | 996 |
rs200959496 | in-del | -/TTAAT | 0.0263992 | 0.111815 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118624 | AGGATGTCAAACTAC[-/TTAAT]TTAATTTCTGTAAAA | 996 |
rs200963865 | snp | A/C | | | splice-donor-variant | CDC27 | GRCh38.p7 | 17:47156911 | TATCTTGTTTGACTT[A/C]CCTTGGGGTTAATGG | 996 |
rs200965819 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160309 | CTCGGCTCACTGCAA[C/G]CTCCACCTTCTGGAT | 996 |
rs200968250 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139472 | CAGGGTTTCACCATG[G/T]TAGCCAGGATGGTCT | 996 |
rs200969858 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133060 | ACACACACACATACA[C/T]ATACACACACACACA | 996 |
rs200982071 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133562 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAT | 996 |
rs200992815 | in-del | -/TCACTCTG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134522 | TTTTGAGATGGAGTC[-/TCACTCTG]TTGCCATGCTGGAGT | 996 |
rs201009764 | snp | A/G | 0.000297069 | 0.0121839 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137193 | TCTGATAGCATTTCG[A/G]AAACAAGCTAATGCT | 996 |
rs201024697 | in-del | -/AGG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130259 | GAGCTACTTGGGAGG[-/AGG]CTGAGGCAGGAGAAT | 996 |
rs201040580 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47130378 | AATAAAAATAAAAAT[-/A]AAAAAAAGAGAAAAA | 996 |
rs201075752 | snp | C/T | 0.0281144 | 0.115181 | intron-variant | CDC27 | GRCh38.p7 | 17:47137118 | TACCAGCACCATCAA[C/T]ACGACTTTGTCTTTG | 996 |
rs201087179 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148953 | GCATGATAGCACATG[C/T]CTGTAATCCCAGCTA | 996 |
rs201098929 | snp | A/G | 1.6525e-05 | 0.00287441 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157252 | TCCTGGGGTGTTTCC[A/G]TAAGAACTGTCTCAG | 996 |
rs201122029 | snp | A/C | 0.00199804 | 0.0315441 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154705 | GGTGGATGGCACATC[A/C]ATTACAGGAGGTGTA | 996 |
rs201126146 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161561 | TTCGAGACCAGCCTG[A/G]CCAACACGGTGAAAA | 996 |
rs201136602 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125258 | TTTTTTTTTTTTTTT[C/T]TTTTTTGAGATGGCG | 996 |
rs201137275 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144870 | TGCATGTGTGTGTAT[A/G]TCACACACACACACA | 996 |
rs201141157 | snp | C/T | 0.000247523 | 0.0111221 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47170001 | TGGCTTTTCTGCTTA[C/T]TAAACACTCCACCAG | 996 |
rs201152963 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143962 | GATGTAATAGTGGGG[A/C]TCAATACCTGAGGTG | 996 |
rs201159396 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130136 | GGAGGCCAAGGCAGG[C/T]GGATCACGAGGTCAG | 996 |
rs201167280 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186760 | CATTAAAACTTTAAA[-/G]AAAAAAAAATGCAGA | 996 |
rs201187810 | snp | G/T | 0.0232499 | 0.105283 | CDC27 | 17 | allele_origin=G(germline)/T(somatic) | 17:47157066 | ATATAAGACACTGAG[G/T]AATCTGTATTCAAGG | 996 |
rs201191792 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150830 | CTGAGGTTGGGAGTT[C/T]GAGACCAGCCTGACC | 996 |
rs201199955 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183380 | CAAGTAAATGTTTAA[-/T]AATTCTGCAATGAGT | 996 |
rs201202261 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130714 | ACCCCCGTCTCTACT[A/G]AAAATACAAAAAATT | 996 |
rs201208180 | in-del | -/TT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134307 | CTAAACCCATATAGA[-/TT]TTTTTTTTTTTTTTA | 996 |
rs201209799 | snp | A/T | 0.00199805 | 0.0315441 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154784 | AATGGCAAAATCCCA[A/T]AACTGAGAAGAGGTT | 996 |
rs201212063 | in-del | -/TATTTTT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156621 | CCCAGCTAATTTTTG[-/TATTTTT]AGTAGAGACAGGGTT | 996 |
rs201216462 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136473 | TTATGGCTTCAGAAT[C/T]ATACCTTATCTTGAT | 996 |
rs201218251 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147163 | CCCAGCACTTTGGGA[G/T]GCCGAGACGGGCGGA | 996 |
rs201230368 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158931 | GCCTTTTTGTATTTT[-/G]CGTCGAGATGGGGTT | 996 |
rs201236032 | in-del | -/TC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137797 | ACCTCTGAACCTCAT[-/TC]TCTCTCTCTTTTTTT | 996 |
rs201293466 | snp | C/T | 0.00593145 | 0.0541345 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137342 | GCAGACTGAAACAGT[C/T]CCCTGCAGCACACCA | 996 |
rs201296720 | snp | A/T | 0.00199801 | 0.0315438 | intron-variant | CDC27 | GRCh38.p7 | 17:47141845 | ATATAACCATTTTCT[A/T]TACTTACTTGCATGT | 996 |
rs201303434 | snp | G/T | 0.00302436 | 0.038769 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169945 | CCAACAATGAAAGAG[G/T]AAAGCAAGCTGAATC | 996 |
rs201309315 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161744 | GACAGAGCGAGACTC[C/T]GTCTCAAATAAATAA | 996 |
rs201314539 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161495 | GTGGCTCATGCCTGT[A/C]ATCTCAGCACTTTGG | 996 |
rs201321536 | snp | G/T | 0.000625407 | 0.0176724 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143915 | CACTAGTAAAGAGTC[G/T]TGAACTTCTTCGAGG | 996 |
rs201322653 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140355 | CTGAGCTCAAGTGAT[C/T]CCCCTTCCTTGGCCT | 996 |
rs201331122 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134348 | CTTGCTCTGTCGCCC[A/G]GGCTGGAGTGCAATG | 996 |
rs201336226 | snp | A/G | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141857 | TCTATACTTACTTGC[A/G]TGTACTCTGAAAGTT | 996 |
rs201351582 | snp | C/T | 0.047771 | 0.146981 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154704 | CGGTGGATGGCACAT[C/T]AATTACAGGAGGTGT | 996 |
rs201366386 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136939 | CTGTTGAGTATAAGG[A/G]TCTGGTATTCTATTA | 996 |
rs201385499 | in-del | -/CG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137135 | GACTTTGTCTTTGTA[-/CG]CTTCATTACCACTTA | 996 |
rs201391440 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161731 | TCCAGCCTGGGTGAC[-/A]AGAGCGAGACTCTGT | 996 |
rs201397588 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180970 | AAAAAAAAAAAAAAA[A/T]ACATGGCATGGTGGC | 996 |
rs201398298 | snp | C/T | 0.041118 | 0.137362 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142373 | CTCCTTTATTAGTTT[C/T]ACTTTTTGTTTTTCT | 996 |
rs201416822 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147138 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 996 |
rs201421257 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147335 | ACCCGGGAGGCGGAG[C/G]TTGCAGTGAGTCGAG | 996 |
rs201424193 | in-del | -/AC/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123401 | CTACTTTTTTTTCTA[-/AC/C]CTTTTTTTTTTTTTT | 996 |
rs201442130 | in-del | -/TTG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160004 | AACCTCTGCTTCTTT[-/TTG]TTTTTTTTTTTCAAA | 996 |
rs201447460 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151843 | GTGTTTGTGCAAGAA[C/T]TGGAGTTACCTCTCG | 996 |
rs201461275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134764 | CAGGCGTGAGCCACC[A/G]TGCCCGGCCTTAATT | 996 |
rs201468566 | snp | C/T | 1.65971e-05 | 0.00288067 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141955 | CAAAATATTTATAGC[C/T]TCTTTGCAGTTGTAT | 996 |
rs201479165 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176916 | AATCTGGTAAATAAG[-/T]TTTTTTTTTATATGT | 996 |
rs201490378 | snp | A/G | 0.000466527 | 0.0152658 | intron-variant | CDC27 | GRCh38.p7 | 17:47157224 | ACTAGAATATAAGAC[A/G]CTTACAATTGTGTCC | 996 |
rs201495927 | in-del | -/AG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135635 | TTGCTCAGTATTTAG[-/AG]TTACCTAAATACGTC | 996 |
rs201503928 | in-del | -/ATATATAT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133107 | CACACACAAATATAC[-/ATATATAT]ATATATATATATATA | 996 |
rs201519931 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158270 | AAGGCTCTTTTGGTA[A/G]CATTCTGATCCTTTG | 996 |
rs201530600 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136895 | AAAAACAACTACAGT[A/G]TCTGCAAAAGTTTGG | 996 |
rs201562778 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174100 | TCTGTTTAAATAAAT[-/A]AAATAAATATAATGA | 996 |
rs201594266 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151814 | TAAATACCTTGTTTG[C/T]GGACCAGAACTTTGT | 996 |
rs201599370 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47170330 | AGCCTTGTGAGTAGC[-/T]GGGACTACAGGTGCA | 996 |
rs201601589 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155336 | TGCAACCTCCACCTG[-/C]CTGGGTTCAAATGAT | 996 |
rs201607934 | snp | A/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138881 | CTAACCTCTGAGAAT[A/T]TTCTTTCAGCCTGAA | 996 |
rs201607944 | in-del | -/TGCTTTTT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133777 | TTTTTGAGACAGTCT[-/TGCTTTTT]GTCACCCAGGTTGGA | 996 |
rs201613328 | snp | A/C | 0.000215022 | 0.0103665 | splice-donor-variant | CDC27 | GRCh38.p7 | 17:47156912 | ATCTTGTTTGACTTA[A/C]CTTGGGGTTAATGGA | 996 |
rs201627057 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158893 | CCAAAATGCTGGGAT[G/T]ACAGGTGTGAGCCAC | 996 |
rs201646524 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133809 | GTTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 996 |
rs201672676 | in-del | -/GAT | 0.0980476 | 0.198521 | intron-variant | CDC27 | GRCh38.p7 | 17:47135408 | TCATGGCCATAACTA[-/GAT]GATGATGATGATGAT | 996 |
rs201679109 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177859 | TTATATGTGTGTGTA[C/T]ACACACACACACACA | 996 |
rs201694245 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163978 | CGTGTTGGCCAGGCT[A/G]GTCTCGAACTCTTGA | 996 |
rs201703180 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142949 | CCAAAGTGCTGGGAT[G/T]ACAGGCATGAGCCAC | 996 |
rs201711178 | snp | G/T | 0.00299549 | 0.0385846 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151859 | TGGAGTTACCTCTCG[G/T]CTATTTCCACTCTGT | 996 |
rs201714005 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135649 | TTAGTTACCTAAATA[C/T]GTCAGCATTTAAACT | 996 |
rs201715412 | snp | C/T | 6.64772e-05 | 0.00576491 | intron-variant | CDC27 | GRCh38.p7 | 17:47129381 | TGAAGACCCTTAAGA[C/T]ATTTATCTTACCTTA | 996 |
rs201720462 | snp | G/T | 0.1792 | 0.239765 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142017 | CACGAAGAAGGCTCA[G/T]CAAACCTTCTAGGAG | 996 |
rs201721869 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157590 | GATAAAGCTGTAAAT[G/T]AAAATAAACTACAAG | 996 |
rs201724426 | snp | C/G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130117 | CTGTAATCTGAGCAC[C/G/T]TTGGGAGGCCAAGGC | 996 |
rs201735152 | snp | A/G | 0.0305196 | 0.119701 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154706 | GTGGATGGCACATCA[A/G]TTACAGGAGGTGTAT | 996 |
rs201746835 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147145 | GTGGCTCACGCCTGT[A/C]ATCCCAGCACTTTGG | 996 |
rs201784583 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147404 | ACTCCGTCTCAAAAA[C/T]AAACAAACAAACAAA | 996 |
rs201793243 | in-del | -/AAGT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175095 | AGGAAGGAAGGAAGG[-/AAGT]AAGTTGTAGCAGCAC | 996 |
rs201803403 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156921 | GACTTACCTTGGGGT[G/T]AATGGACTAAGAGCT | 996 |
rs201804958 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151888 | GTGAGAAGACAGACT[G/T]TGTTCCAGTTTGGCC | 996 |
rs201815594 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136768 | AATTTTTTTTCCTAT[G/T]ATCCAATAAGTGAAT | 996 |
rs201816724 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161650 | AGCTACCTGGGAGGC[C/T]GAGGCAGGAGAACTG | 996 |
rs201822387 | in-del | -/TATTATA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140384 | CTCCCAAAGTGCTGG[-/TATTATA]GGCATGAGCCACCAC | 996 |
rs201826729 | in-del | -/GAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174860 | CTCGGGAGGCTGAGG[-/GAC]CAGAACAATCACTTA | 996 |
rs201829573 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160285 | CAGGCTGGAGTGCAG[C/T]GGCATGATCTCGGCT | 996 |
rs201835938 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151366 | TAAAATGTTAGCTAT[A/T]ATCTATTGAGTCCTT | 996 |
rs201840116 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139324 | CAGGCTGGAGTGCAG[C/T]GGCGCAATCTCGGCT | 996 |
rs201853513 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132100 | ATTCTGTGATTTTTT[A/T]TGCTAAGCCAAATGG | 996 |
rs201896917 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136607 | ATAACAATATGACCT[A/G]GGTAGTAATTTCCTA | 996 |
rs201923531 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139517 | TGTGATCCACCCGCC[C/T]CGGCCTCCCAAAGTG | 996 |
rs201928826 | snp | A/C | 1.66371e-05 | 0.00288414 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138814 | TTTTTGAAGATGCCA[A/C]AGTGTTGTAGAGTAG | 996 |
rs201949920 | in-del | -/A | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117473 | TTTCTCCAAGATACC[-/A]AAAAAAAAAAAATTT | 996 |
rs201967700 | in-del | -/CT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159011 | CCACCACAGCCTCCC[-/CT]AAAATGCTGGAATTA | 996 |
rs201977841 | snp | C/T | 0.0029955 | 0.0385847 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154675 | CATGGAAAATACCTT[C/T]TTTGAAGGGGCTCCG | 996 |
rs202004640 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136853 | TGTTCGAAGAAAAAG[C/T]AACAAAGTAACAAAA | 996 |
rs202013191 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176234 | TTCTATTTCATCAAC[-/T]TTTTTTTTTTCTGTT | 996 |
rs202016550 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142793 | AAGCGATTCTCCTGC[C/T]TCAGCCTCCCGCGTA | 996 |
rs202020147 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173842 | TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 996 |
rs202026262 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136191 | TTCTTAAAATATTAC[A/G]GAGAACATAGCTATC | 996 |
rs202030153 | snp | A/G | 4.89524e-05 | 0.0049471 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142332 | TGTAATTTCCAGGCT[A/G]TCATTTATGTTAGGT | 996 |
rs202044028 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144031 | TTTACTTGATTTATG[A/G]CCATTAACCATTGTT | 996 |
rs202052665 | snp | A/G | 0.227678 | 0.249001 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141918 | CCCAACCAGTATTGT[A/G]GTGGTGAGAAGGTAG | 996 |
rs202065276 | in-del | -/TC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134085 | TAATTTTTTGTGGAG[-/TC]ACGAGGTCTCACTAT | 996 |
rs202094301 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130143 | AAGGCAGGTGGATCA[C/T]GAGGTCAGGAGATCG | 996 |
rs202100614 | snp | C/T | 0.000219541 | 0.0104748 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157118 | CTAAATTCAATCTGT[C/T]TAATTCCTGAAACAG | 996 |
rs202105785 | in-del | -/CCA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134348 | TTGCTCTGTCGCCCG[-/CCA]GGCTGGAGTGCAATG | 996 |
rs202120807 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168235 | CTCACCTCCTGGGAG[C/G/T]TTGCGGGGTGGGGAT | 996 |
rs202126011 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135964 | GCTAACATGGTGAAA[C/T]CCCGTCTCTACTAAA | 996 |
rs202161114 | in-del | -/ACCT | 0.0279526 | 0.114869 | intron-variant | CDC27 | GRCh38.p7 | 17:47144994 | AGCAAATGACACACA[-/ACCT]ACCTTTCTTGGATGA | 996 |
rs202164898 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161499 | CTCATGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 996 |
rs202172905 | in-del | -/AGGAAGGA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175040 | GAGAAAGAGAGAGAG[-/AGGAAGGA]AGGAAGGAAGGAAGG | 996 |
rs202182614 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157354 | TGTAAAGATGTGAAT[C/T]TAAATGTTTGGTCAG | 996 |
rs202185735 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178841 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 996 |
rs202188863 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139395 | CCTCAGCCTCCCAAG[C/T]AGCTGGGACTACAGG | 996 |
rs202191622 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133062 | ACACACACATACATA[C/T]ACACACACACACACA | 996 |
rs202241282 | in-del | -/ACAGC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126098 | TAATTAAATATCAGT[-/ACAGC]ACATTAAATAAGGTG | 996 |
rs367624910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47182573 | TTTACTTTTTCCTGT[C/T]TTTGAACTTTAAATA | 996 |
rs367644695 | snp | A/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157300 | CTATGATTAGGTACT[A/T]GTGTTGTGCAAGAGT | 996 |
rs367664829 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47127126 | AGACTCCAGTTAGAT[-/A]AAAAAAATTAGCTGA | 996 |
rs367705594 | in-del | -/TCTC | 0.029116 | 0.117091 | intron-variant | CDC27 | GRCh38.p7 | 17:47170150 | GAGACACAAATTTTT[-/TCTC]TCTCTCTCTTTCCTT | 996 |
rs367779900 | in-del | -/ATATAT | 0.206336 | 0.246157 | intron-variant | CDC27 | GRCh38.p7 | 17:47133107 | CACACACAAATATAC[-/ATATAT]ATATATATATATATA | 996 |
rs367805919 | snp | C/G | 0.000149757 | 0.00865193 | intron-variant | CDC27 | GRCh38.p7 | 17:47124006 | GCAAAAATTTTTAAA[C/G]TTTTGACCAAGCGTT | 996 |
rs367809956 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157711 | AAGTAGGAGATGAGG[C/T]TGAAGAGTTAAAACC | 996 |
rs367856634 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136861 | GAAAAAGCAACAAAG[G/T]AACAAAACTAAACAA | 996 |
rs367910677 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129994 | CTTCTCAAAACTGTG[A/T]TAACACTCCTGTTTA | 996 |
rs367926175 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147228 | ACACGGTGAAACCCC[C/G]TCTCTACTAAAAATA | 996 |
rs367927544 | in-del | -/AAA | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47129997 | TCAAAACTGTGTTAA[-/AAA]CACTCCTGTTTACAA | 996 |
rs368006079 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140756 | TAAAGGACCATAATC[A/G]AAACATGGGTTTTGT | 996 |
rs368016453 | snp | C/T | 0.000100308 | 0.00708122 | intron-variant | CDC27 | GRCh38.p7 | 17:47129541 | AAGAAATAAAGATCA[C/T]GTTAATACTCCCTCT | 996 |
rs368042550 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160708 | ATATATAAAGGACCA[G/T]AAGAAATCTAACCGA | 996 |
rs368043685 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177825 | ATGTCTGGTTGATTT[C/T]CTGAACATAACTCTT | 996 |
rs368048550 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47159579 | AGTAGCCTCTGCGCA[C/G]GGGGACAATCGAGAG | 996 |
rs368080491 | snp | C/T | 1.83018e-05 | 0.00302499 | intron-variant | CDC27 | GRCh38.p7 | 17:47170079 | ATTTTTAAAAACCAA[C/T]ATAAAAAGCAGTTCA | 996 |
rs368113433 | in-del | -/C | 0.0517044 | 0.152246 | intron-variant | CDC27 | GRCh38.p7 | 17:47137806 | CCTCATTCTCTCTCT[-/C]TTTTTTTTTTTTGAG | 996 |
rs368174839 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142895 | TGGTCAGGCTGGTCT[C/G]GAACTCCTGACCTTA | 996 |
rs368193891 | snp | G/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189515 | AGCCACGCACACCAC[G/T]CCCAATCGGCCGTCC | 996 |
rs368256588 | snp | A/C | 4.19463e-05 | 0.00457945 | intron-variant | CDC27 | GRCh38.p7 | 17:47181514 | AAGTTATGGAATTTC[A/C]TATATGTTATTCATT | 996 |
rs368294576 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136758 | AAATTTTTTCAATTT[A/T]TTTTCCTATTATCCA | 996 |
rs368304141 | snp | C/G | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157314 | TTGTGTTGTGCAAGA[C/G]TTGGGCAGACAGTTG | 996 |
rs368324912 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124980 | TGGAGTGCAGTGGTG[C/T]GATCTCTGCTCACTG | 996 |
rs368329572 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131700 | AAGAGATGGAGTCTC[A/G]TTCTGTTGCCCAGGC | 996 |
rs368488170 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131759 | CAGCAGCCTTGCACT[C/T]CTGGGCTCAAGTGAT | 996 |
rs368551618 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131772 | CTCCTGGGCTCAAGT[A/G]ATCCTTGTGCTTCAG | 996 |
rs368559383 | snp | C/G | 5.06308e-05 | 0.00503119 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189204 | CACTTTCTGCAGTGC[C/G]TCAGGCCCCCCCTGT | 996 |
rs368560459 | snp | A/G | 8.34857e-05 | 0.00646033 | intron-variant | CDC27 | GRCh38.p7 | 17:47138694 | CTATCTGTTGAGGGT[A/G]ATCAAAAAGGTAACT | 996 |
rs368566307 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151538 | CTAAACTATAGAAAG[A/G]GTCATGTGCATAAGA | 996 |
rs368594485 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134805 | TTTTTTTTTTTTTTT[-/G]TTAGGGAAGGGGTCT | 996 |
rs368750026 | snp | G/T | 1.64808e-05 | 0.00287057 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157292 | GAGATAAACTATGAT[G/T]AGGTACTTGTGTTGT | 996 |
rs368926843 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181294 | AAAAAAAACCCAAAA[A/C]AACAAAAACCCTGGG | 996 |
rs368935549 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118295 | TCAAATGTTACTTGT[A/G]GTTCTCGGAAAAATT | 996 |
rs368943114 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186711 | GACGGAGTTTTAATT[C/T]AGGCATATATGGTAT | 996 |
rs368968887 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131718 | CTGTTGCCCAGGCTG[G/T]AGTGCAGTATCACCT | 996 |
rs369006854 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141575 | TAAATATAAATATGT[A/C]TTTTCAGACACAACT | 996 |
rs369014344 | snp | A/T | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117352 | GGGAAGGTTATGAGG[A/T]CTGCATTGTTCCCCT | 996 |
rs369065482 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131779 | GCTCAAGTGATCCTT[C/G]TGCTTCAGCCTCCCA | 996 |
rs369068321 | snp | A/G | 0.000228646 | 0.0106897 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154741 | GTAGTTTTGTAAATA[A/G]GATCCATCTCCAGGA | 996 |
rs369161217 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128063 | TGTGAGACAGAGTGT[C/T]GCTGTTGCCCAGGCT | 996 |
rs369181174 | snp | C/T | 7.20955e-05 | 0.00600354 | intron-variant | CDC27 | GRCh38.p7 | 17:47157153 | TTTCTACCAAGTCAT[C/T]CACAATATATTATTT | 996 |
rs369185345 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131729 | GCTGGAGTGCAGTAT[C/T]ACCTTCTTAGCTCAC | 996 |
rs369215989 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149123 | AAATTCTTGCCTAGT[A/G]AAAATATTGTTCAAA | 996 |
rs369249410 | snp | A/T | 1.67125e-05 | 0.00289067 | missense, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151931 | AGACTGTAAAACACG[A/T]AAAGTCTAAGGTTTG | 996 |
rs369263739 | in-del | -/AATC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136857 | GAAGAAAAAGCAACA[-/AATC]AAGTAACAAAACTAA | 996 |
rs369264197 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179712 | AAATATGGTTAAACC[C/G]AATGGTGAGGTTCTA | 996 |
rs369302713 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145175 | ATGGTTTTCAGACAC[C/T]GGACAATAGGCAAAA | 996 |
rs369407748 | in-del | -/T | 0.473726 | 0.111565 | intron-variant | CDC27 | GRCh38.p7 | 17:47134307 | CTAAACCCATATAGA[-/T]TTTTTTTTTTTTTTT | 996 |
rs369448767 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165260 | GGCTTTTATGAATAA[A/C]GTTGCTATGAACTCC | 996 |
rs369501361 | snp | A/G | 1.70035e-05 | 0.00291572 | intron-variant | CDC27 | GRCh38.p7 | 17:47129569 | TCTTGATATTTATGA[A/G]GAAAGGTGAGAACCA | 996 |
rs369524997 | snp | C/T | 8.44245e-05 | 0.00649655 | intron-variant | CDC27 | GRCh38.p7 | 17:47151782 | TTATGCCAAGAAAAG[C/T]TGAATAATTACAATG | 996 |
rs369577736 | in-del | -/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118785 | TTACTACGTGGGAAA[-/T]TAAGGCTTCAAATAC | 996 |
rs369585038 | snp | C/T | 2.67598e-05 | 0.00365776 | intron-variant | CDC27 | GRCh38.p7 | 17:47181673 | ACATAAATATACATA[C/T]ATACAGACTTTCAAG | 996 |
rs369614908 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133024 | ATATATATATATATA[C/T]ATATACACACACACA | 996 |
rs369624230 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159552 | CGTAGGGCTTGCCAA[C/T]CTTGTTCCCCCAGTA | 996 |
rs369639656 | snp | C/G/T | 4.96285e-05 | 0.00498118 | synonymous-codon, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122577 | CATCAGGGCGAGGTG[C/G/T]GTTTGACCTAACTTC | 996 |
rs369759236 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131733 | GAGTGCAGTATCACC[A/T]TCTTAGCTCACAGCA | 996 |
rs369869167 | in-del | -/AGAAACACACAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136872 | AAGTAACAAAACTAA[-/AGAAACACACAC]ACAAACAAAAAACAA | 996 |
rs369880455 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47179297 | AGGAGGCCCCTGAGC[A/C]AACAGGTTACATCTA | 996 |
rs369887414 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164237 | GTGTAGTAGGCTACA[A/C]CATCTAGGTTTGTGC | 996 |
rs369894719 | in-del | -/CT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148449 | GCAACTTCAAGCAAT[-/CT]AATATACAAGTACCT | 996 |
rs369929300 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168077 | CAGGAACCTCCATGT[A/G]TTCAGTTTTCTGGAA | 996 |
rs369937187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47141264 | TCTTTTTTTAAGTTG[A/G]GGGTGGAGAAAATGC | 996 |
rs369988089 | snp | A/C | 0.433438 | 0.169854 | intron-variant | CDC27 | GRCh38.p7 | 17:47157394 | TTTCACCTGTGAAGA[A/C]AAAAAAAAAAAAAGT | 996 |
rs370085817 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144439 | TCATTTGCAACTACA[A/T]CAAGTTAGAGAAAAA | 996 |
rs370098078 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CDC27 | GRCh38.p7 | 17:47122427 | TAAATACTCAAAATC[A/G]TATGTATGATACTTA | 996 |
rs370101394 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174177 | ACACGGGTGGTTTCT[C/T]AGGCTCCTCACAAGT | 996 |
rs370133846 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186576 | GTCACTTAGGCTAGT[A/G]TGTCTTTCCAAATAG | 996 |
rs370159272 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124288 | ATCTATCTATCTATT[C/T]ATTTTTATTTATTGA | 996 |
rs370261409 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157297 | AAACTATGATTAGGT[A/C]CTTGTGTTGTGCAAG | 996 |
rs370273617 | snp | A/G | 5.00755e-05 | 0.00500352 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189105 | TGCTGCTTCCCGACC[A/G]AGGCTGCCAGCCAAG | 996 |
rs370285264 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136876 | TAACAAAACTAAACA[A/C]ACAAAAAACAACTAC | 996 |
rs370370566 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136187 | TGAGTTCTTAAAATA[G/T]TACAGAGAACATAGC | 996 |
rs370375834 | in-del | -/ATAAAAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136883 | CTAAACAAACAAAAA[-/ATAAAAC]ACAACTACAGTATCT | 996 |
rs370382588 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131749 | TCTTAGCTCACAGCA[A/G]CCTTGCACTCCTGGG | 996 |
rs370497768 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47175313 | TTATAATCTAAATAA[C/G]CAGCCTTTCTAAAAT | 996 |
rs370507003 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151102 | GTGAAATGTACAAAT[C/T]GGAAATTATTTTTAC | 996 |
rs370544866 | snp | A/C | 0.0535932 | 0.154675 | intron-variant | CDC27 | GRCh38.p7 | 17:47147432 | AAACAAACAAACAAA[A/C]AAAAAAACACTAGGC | 996 |
rs370555651 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147196 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 996 |
rs370562138 | in-del | -/TTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132742 | AGCCATTAAAGCAGT[-/TTA]TTATTATTATTATTA | 996 |
rs370562787 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119666 | GTTTAAATCTGTTAC[C/T]GTGGAATTCCAATAA | 996 |
rs370570999 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160339 | TTCAAGTGATTCTCA[G/T]GCCTCAGCCTCCCGA | 996 |
rs370592021 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131755 | CTCACAGCAGCCTTG[C/T]ACTCCTGGGCTCAAG | 996 |
rs370648589 | in-del | -/TTATTATTG/TTATTG/TTG | 0.301177 | 0.244706 | intron-variant | CDC27 | GRCh38.p7 | 17:47132777 | TTATTATTATTATTA[-/TTATTATTG/TTATTG/TTG]TTATATTTTAAAGAT | 996 |
rs370661352 | in-del | -/AA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131841 | GCCAGGCTAATTTTT[-/AA]ATTTTTTTTGTAGAG | 996 |
rs370698835 | snp | A/C | 3.51031e-05 | 0.00418931 | intron-variant | CDC27 | GRCh38.p7 | 17:47169871 | AAACTATAAAACATA[A/C]TTGTATGGAAATGCT | 996 |
rs370796383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47180106 | GTACTCTAGCCTGGG[C/T]GACAGAGTGAGATTC | 996 |
rs370811783 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136198 | AATATTACAGAGAAC[A/G]TAGCTATCGGAAGAG | 996 |
rs370828137 | snp | C/T | 3.67992e-05 | 0.00428932 | missense, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120988 | CATCCGCATCTGTCA[C/T]GCTGCTCTCCTGGGA | 996 |
rs370849730 | snp | A/G | 8.28658e-05 | 0.00643631 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157243 | ACAATTGTGTCCTGG[A/G]GTGTTTCCGTAAGAA | 996 |
rs370852153 | in-del | -/GTTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174604 | ATCAATCGTGTACTA[-/GTTA]AATTATGCTATGTCC | 996 |
rs370898217 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182559 | TAAGCAGTATAACAT[C/T]TACTTTTTCCTGTTT | 996 |
rs370931760 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139635 | CTATTTTTGAACAAT[C/T]TTTACCGAGAGGTTG | 996 |
rs370953694 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47181304 | CAAAACAACAAAAAC[C/T]CTGGGGGAAAAAAAA | 996 |
rs370974520 | snp | A/G | 8.06712e-05 | 0.00635052 | intron-variant | CDC27 | GRCh38.p7 | 17:47138924 | AGTAAGAGAAAACAA[A/G]TTGATACAATTTATA | 996 |
rs371051872 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124370 | CTCTCTGCAATCTCC[A/G]CTTCTCAGATTCAAG | 996 |
rs371071302 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188283 | TACCAAGGCACAAAA[C/G]ATACAGTTTCTCCAG | 996 |
rs371074533 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173874 | GAGGCAGGCAGATCA[C/T]CTGAGGTCAGGAATT | 996 |
rs371075468 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164129 | TACACAAATATTTAC[C/T]ATACTGTTATAACTG | 996 |
rs371098155 | snp | A/G | 1.66241e-05 | 0.00288302 | intron-variant | CDC27 | GRCh38.p7 | 17:47129380 | CTGAAGACCCTTAAG[A/G]TATTTATCTTACCTT | 996 |
rs371143410 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151432 | TGTGTGGAAATAGAT[G/T]CATTATTTGAAGTTT | 996 |
rs371172648 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131727 | AGGCTGGAGTGCAGT[A/G]TCACCTTCTTAGCTC | 996 |
rs371268313 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47165507 | CAATTGTTTTACTTA[-/T]TTTCTAATTGAACTG | 996 |
rs371268834 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148681 | ACAGAGAAAAGACAT[A/C]TTACTACATATAGAG | 996 |
rs371272674 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133737 | GCATGAGCCACCACA[C/T]CTGGCCTACATATAT | 996 |
rs371289217 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127315 | GTAAAAATAGAAACC[C/T]GTGTCTTCATAAAGA | 996 |
rs371365716 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131775 | CTGGGCTCAAGTGAT[C/T]CTTGTGCTTCAGCCT | 996 |
rs371441950 | snp | C/T | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190762 | GGCCTGGAAAGTAGC[C/T]ATTAGCTATTTAAAG | 996 |
rs371455344 | snp | C/T | 1.65411e-05 | 0.00287581 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132262 | AGCTACTTACTACTC[C/T]AATGTGGCAAAGTAA | 996 |
rs371540265 | snp | C/G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136969 | TCTTTAACAAACTCT[C/G/T]AAATTAACTAATGAT | 996 |
rs371541503 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177256 | GGAGATCTTGACTTA[A/C]AAAAAAATGTTTAAA | 996 |
rs371549435 | snp | A/G | 3.29848e-05 | 0.00406095 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47170016 | TTAAACACTCCACCA[A/G]ATAAGATTTGTTCCC | 996 |
rs371553662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47131642 | ACAAACATAATGTAC[A/G]TATCTTTTCTCCTGT | 996 |
rs371568135 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160733 | AACCGAGATCCTCAA[A/C]TGAAACTATCAGGTA | 996 |
rs371622399 | snp | A/C | 4.64026e-05 | 0.00481655 | intron-variant | CDC27 | GRCh38.p7 | 17:47172099 | AAAAAGGCTATTGTT[A/C]AGTATATTGAATGAT | 996 |
rs371671546 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136879 | CAAAACTAAACAAAC[A/C]AAAAACAACTACAGT | 996 |
rs371698926 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166144 | GGAATAGTGGCCTAT[A/G]GTTTTCCTTTTTAGA | 996 |
rs371748410 | snp | G/T | 5.25767e-05 | 0.00512695 | intron-variant | CDC27 | GRCh38.p7 | 17:47151978 | CTGTAAATGATAAAA[G/T]ACAACACAACGCTCC | 996 |
rs371833525 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131843 | CAGGCTAATTTTTAA[A/G]TTTTTTTTGTAGAGA | 996 |
rs371941195 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120229 | AATTTTAAAGTTTGC[A/G]ATACCAAGACAACAA | 996 |
rs371945511 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189225 | CCCCCCCTGTAGCGG[A/C]TCCGGCCCGGCCAGC | 996 |
rs371956906 | snp | A/C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142750 | TAATTCTCAGCTCAC[A/C/T]GCAACCCAACCTCTG | 996 |
rs372057526 | snp | A/G | 0.000100214 | 0.00707791 | missense, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151930 | CAGACTGTAAAACAC[A/G]AAAAGTCTAAGGTTT | 996 |
rs372112572 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185130 | ATATTATTTAAAATA[C/T]AAACAAACCTCTATA | 996 |
rs372149135 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182395 | ACTCACCACCCAGCT[C/T]AAGAAATAAAATATC | 996 |
rs372162279 | snp | C/T | 4.28734e-05 | 0.00462978 | intron-variant | CDC27 | GRCh38.p7 | 17:47156869 | GAGTTATCATAAGAT[C/T]ATTTGGTATTATAGC | 996 |
rs372204129 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47184128 | TGCTCAAATTTGTGT[C/G]CCAGCACTTCCAGTA | 996 |
rs372204712 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131185 | CCTATTTTTAAAAAA[-/A]GTGTTCAACTTCACC | 996 |
rs372212798 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157307 | TAGGTACTTGTGTTG[C/T]GCAAGAGTTGGGCAG | 996 |
rs372307237 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131765 | CCTTGCACTCCTGGG[C/T]TCAAGTGATCCTTGT | 996 |
rs372342211 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144321 | AGATTATAGCATAGA[A/T]CTTCACTCTCTCTGA | 996 |
rs372353301 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129342 | GAAAACAAGGGATAA[C/T]GTTGTTTTTAAGCAA | 996 |
rs372444182 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131701 | AGAGATGGAGTCTCA[C/T]TCTGTTGCCCAGGCT | 996 |
rs372445288 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142439 | TTTTGCTATTCTCCT[C/G]TAAAAGGGAAGAAAT | 996 |
rs372500200 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129995 | TTCTCAAAACTGTGT[A/T]AACACTCCTGTTTAC | 996 |
rs372519488 | in-del | -/GA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175042 | GAAAGAGAGAGAGAG[-/GA]AGGAAGGAAGGAAGG | 996 |
rs372592988 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168486 | CTATTATAAACCTTT[A/G]AGGGTGGGGACTGTG | 996 |
rs372605318 | snp | A/C/G | 4.03967e-05 | 0.00449408 | intron-variant | CDC27 | GRCh38.p7 | 17:47137116 | AGTACCAGCACCATC[A/C/G]ATACGACTTTGTCTT | 996 |
rs372624751 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147767 | TCAGCCACATGTGGT[A/G]GCATGTGCCTGTAGT | 996 |
rs372647297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141336 | TTTTCTTTGGCTTTA[A/G]GTTAATCATTCTCTC | 996 |
rs372666898 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136865 | AGCAACAAAGTAACA[-/C]AAACTAAACAAACAA | 996 |
rs372689190 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123648 | AACTCCTGACCTCAC[A/G]TAATCTACCTGCCTA | 996 |
rs372743228 | snp | C/T | 0.000183384 | 0.00957383 | intron-variant | CDC27 | GRCh38.p7 | 17:47138705 | GGGTGATCAAAAAGG[C/T]AACTATATAAGCAAA | 996 |
rs372768411 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148198 | AGCGAGACTCTATCT[A/C]AAAAAAAAAAAAAAA | 996 |
rs372774440 | snp | A/G | 8.27397e-05 | 0.00643141 | missense, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122578 | ATCAGGGCGAGGTGC[A/G]TTTGACCTAACTTCT | 996 |
rs372829187 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143455 | GTGTATGTGTGTGCA[C/T]AGTTCTATAAAATTT | 996 |
rs372895332 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136188 | GAGTTCTTAAAATAT[G/T]ACAGAGAACATAGCT | 996 |
rs372926889 | in-del | -/GCG | | | cds-indel, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157305 | TTAGGTACTTGTGTT[-/GCG]GTGCAAGAGTTGGGC | 996 |
rs372949976 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181297 | AAAAACCCAAAACAA[A/C]AAAAACCCTGGGGGA | 996 |
rs372994587 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141586 | ATGTATTTTCAGACA[C/G]AACTGAATAGGACAC | 996 |
rs373060646 | snp | C/T | 5.02121e-05 | 0.00501034 | intron-variant | CDC27 | GRCh38.p7 | 17:47122430 | ATACTCAAAATCATA[C/T]GTATGATACTTACTG | 996 |
rs373074410 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169646 | GTGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 996 |
rs373086500 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47152658 | TTTTCTTCAAAACTT[A/C]CTGTTACCCTGATGT | 996 |
rs373098075 | in-del | -/GCAT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136876 | AACAAAACTAAACAA[-/GCAT]ACAAAAAACAACTAC | 996 |
rs373116386 | snp | C/T | 0.000165862 | 0.00910514 | intron-variant | CDC27 | GRCh38.p7 | 17:47132408 | GTATAATTTTAAAAA[C/T]ATAAAGTTTAGGTTG | 996 |
rs373126557 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47126595 | CTTGGGTTTCTTGAA[A/G]CAAGTAAACGCTGAT | 996 |
rs373129272 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166155 | CTATAGTTTTCCTTT[C/T]TAGAACAGTATTTCA | 996 |
rs373154965 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47187598 | TAAGCCACCACGCCC[A/G]GCCTTCCATGCTTTT | 996 |
rs373163271 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172287 | AAGAAACCAAGGAAA[G/T]AATACAATGAAGACA | 996 |
rs373225595 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150004 | AAAGACAACTGACTG[C/T]TTAAGGCAGAAACCA | 996 |
rs373299731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138316 | AGATATGTTACAAAA[C/G]TATCATTAAATATTT | 996 |
rs373303822 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131730 | CTGGAGTGCAGTATC[A/G]CCTTCTTAGCTCACA | 996 |
rs373344958 | snp | A/G | 5.25785e-05 | 0.00512704 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181577 | CTTCTGCATAAAGGC[A/G]TTCTGCGAGGAAAAC | 996 |
rs373381028 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164795 | GTACTCCAGCCTGAG[A/C]GACAGAGCGCAAGAT | 996 |
rs373429427 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137939 | CCGAGCAGCTGGGAC[C/T]ACAGATGCCAGCCAC | 996 |
rs373527070 | snp | C/T | 2.94286e-05 | 0.00383581 | intron-variant | CDC27 | GRCh38.p7 | 17:47181683 | ACATACATACAGACT[C/T]TCAAGGTAACTACTA | 996 |
rs373549470 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178797 | CTGAATTCAGATTCT[C/T]TTTCCTTTTTCCGTT | 996 |
rs373670800 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160695 | ATTCTAAGGTTTTAT[A/G]TATAAAGGACCAGAA | 996 |
rs373677958 | in-del | -/ACAC/ATAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133062 | CACACACATACATAT[-/ACAC/ATAC]ACACACACACACACA | 996 |
rs373686924 | snp | A/G | 0.000118047 | 0.00768178 | intron-variant | CDC27 | GRCh38.p7 | 17:47157160 | CAAGTCATTCACAAT[A/G]TATTATTTAGTTCAG | 996 |
rs373705418 | snp | A/G | 0.00011697 | 0.00764665 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189177 | AGCACCGTCATCCTC[A/G]AGGCTCAGGCCCACT | 996 |
rs373798464 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183019 | GCAAGACTCCCATCA[A/G]AAAAACACAAAAAAG | 996 |
rs373978944 | snp | C/T | 1.65822e-05 | 0.00287938 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156996 | AACCTGTTTAGATAA[C/T]ATGGAAGTTCCTGTT | 996 |
rs374075757 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133026 | ATATATATATATATA[C/T]ATACACACACACACA | 996 |
rs374180360 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136756 | GTAAATTTTTTCAAT[G/T]TTTTTTCCTATTATC | 996 |
rs374220387 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139513 | ACCTTGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 996 |
rs374261629 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156516 | GTAGTGGCTCCATCT[C/T]GGCTCACTACAACCT | 996 |
rs374317486 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142782 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCTTCAG | 996 |
rs374332180 | snp | A/C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189473 | GTCTGACCCAAAGCG[A/C/T]AGGTTTCTCTTCTCA | 996 |
rs374379485 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131699 | TAAGAGATGGAGTCT[C/T]ATTCTGTTGCCCAGG | 996 |
rs374412743 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132304 | GAGGGTTGATATCAA[A/G]CGCTTTTTGGAAATG | 996 |
rs374472811 | snp | A/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157299 | ACTATGATTAGGTAC[A/T]TGTGTTGTGCAAGAG | 996 |
rs374542509 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131771 | ACTCCTGGGCTCAAG[C/T]GATCCTTGTGCTTCA | 996 |
rs374607676 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188607 | CATCATTGTCCGGTG[A/G]GAAATTCACCGAGAA | 996 |
rs374613897 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131737 | GCAGTATCACCTTCT[C/T]AGCTCACAGCAGCCT | 996 |
rs374614181 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157288 | CTGTGAGATAAACTA[G/T]GATTAGGTACTTGTG | 996 |
rs374649873 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131099 | AAGCTTACTCTCTTA[-/A]CCTGACAATTTCTTC | 996 |
rs374665111 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177562 | GACAGAGGGAGACCC[C/T]ATCTGAAACAAACAA | 996 |
rs374697424 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177270 | AAAAAAAAATGTTTA[A/C]AAAGTACTAATATTA | 996 |
rs374698945 | snp | C/T | 0.000140326 | 0.00837517 | intron-variant | CDC27 | GRCh38.p7 | 17:47142061 | AAACAAAGGAAAAAA[C/T]GCAATAAACTAGTCT | 996 |
rs374726979 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131753 | AGCTCACAGCAGCCT[C/T]GCACTCCTGGGCTCA | 996 |
rs374745115 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131756 | TCACAGCAGCCTTGC[A/C]CTCCTGGGCTCAAGT | 996 |
rs374807404 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131778 | GGCTCAAGTGATCCT[C/T]GTGCTTCAGCCTCCC | 996 |
rs374866439 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136856 | CGAAGAAAAAGCAAC[-/T]AAAGTAACAAAACTA | 996 |
rs374897480 | in-del | -/ACG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136950 | AGGATCTGGTATTCT[-/ACG]ATTATCATTAGTTAA | 996 |
rs374993697 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131728 | GGCTGGAGTGCAGTA[G/T]CACCTTCTTAGCTCA | 996 |
rs375064668 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132769 | TTATTATTATTATTA[-/T]TATTATTATTATATT | 996 |
rs375143211 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147312 | GCTGAGGCAGGAGAA[A/T]GGCGTGAACCCGGGA | 996 |
rs375167684 | in-del | -/CAGC | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120751 | AGCCAGTCTTGTTAG[-/CAGC]TAAATATTGCACTGC | 996 |
rs375289721 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129993 | ACTTCTCAAAACTGT[A/G]TTAACACTCCTGTTT | 996 |
rs375381741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47131611 | AGAAGCTAATAAATG[C/T]GATTTTAAAAAGCAA | 996 |
rs375385962 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140577 | AGAAATTAAGTTGAA[A/G]CAGAGGCTTTCTTTA | 996 |
rs375392790 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131707 | GGAGTCTCATTCTGT[C/T]GCCCAGGCTGGAGTG | 996 |
rs375434475 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156285 | CTGGATCTACAGGCG[C/T]GTGCCACCACACCCG | 996 |
rs375494003 | snp | C/T | 0.000269215 | 0.0115989 | intron-variant | CDC27 | GRCh38.p7 | 17:47181524 | ATTTCATATATGTTA[C/T]TCATTTATCATTCTA | 996 |
rs375503037 | snp | A/G | 0.000193981 | 0.00984647 | intron-variant | CDC27 | GRCh38.p7 | 17:47123834 | TTATTCTTATAAAAT[A/G]TCATTATTTGCTATG | 996 |
rs375626715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47151531 | TCTGTACCTAAACTA[C/T]AGAAAGGGTCATGTG | 996 |
rs375653477 | in-del | -/GGC | | | cds-indel, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157307 | AGGTACTTGTGTTGT[-/GGC]GCAAGAGTTGGGCAG | 996 |
rs375733400 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144731 | AACTATCTAAACTTT[A/G]TAATTTATGGGAAAT | 996 |
rs375749345 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120452 | ACTGTTATAGGCAAC[A/G]TCTTTTATTGTTCCA | 996 |
rs375751451 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142965 | ACAGGCATGAGCCAC[C/T]GTGCCCGGCCTTTGT | 996 |
rs375785198 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134909 | GGCTTATAGGTATGA[A/G]CCACCATACCTGTCA | 996 |
rs375919724 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169591 | TGGAGGTTGCAGTGA[A/G]CTGAGATCACACCAT | 996 |
rs376030802 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158620 | CAGTATTATTCTTAA[-/T]TTTTTTTTTTTTTTT | 996 |
rs376078038 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131845 | GGCTAATTTTTAAAT[A/T]TTTTTTGTAGAGATG | 996 |
rs376080277 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167030 | CGGCTAACTTTTTTA[C/T]TTTTAGTAGAGACAA | 996 |
rs376084177 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125437 | TTTTTAGTAGACACG[C/T]GGTTTCACCATATTG | 996 |
rs376084191 | snp | A/G/T | 0.000117555 | 0.00766587 | intron-variant | CDC27 | GRCh38.p7 | 17:47137121 | CAGCACCATCAATAC[A/G/T]ACTTTGTCTTTGTAC | 996 |
rs376106398 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159328 | CCGGGGTCAGGTAGT[C/T]GTAGGTCTTAGAGAT | 996 |
rs376119729 | in-del | -/AGTAGTAT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181398 | TATTAAAAGTAGTAT[-/AGTAGTAT]GTAAGGGAACTACAC | 996 |
rs376251163 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151991 | AAGACAACACAACGC[C/T]CCCATCTACATTTTC | 996 |
rs376251298 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145618 | TGTAAAGGTCAACCA[C/T]GTGGCCGGGCATGGT | 996 |
rs376284085 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128764 | TTTTTCTGTTTTTTA[A/C]TTTTTAATTTTTTTT | 996 |
rs376297134 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181357 | AAGTAAATCATAGCA[C/T]ATAAACCTGAATCAA | 996 |
rs376306346 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148105 | CAGGAGGCTGAGGCA[A/G]GAGAATCGCTTGAAC | 996 |
rs376318111 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136881 | AACTAAACAAACAAA[-/C]AAACAACTACAGTAT | 996 |
rs376322023 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149339 | AACATGGTGAAACCC[C/T]GTTTCTACTAAAAAT | 996 |
rs376328309 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185203 | TTTTTTTTTGAGACA[C/G]AGTCTCACTCTGTCA | 996 |
rs376333382 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136168 | AAACAAACAAAAAAA[A/G]AACTGAGTTCTTAAA | 996 |
rs376392297 | snp | A/G | | | intron-variant, splice-donor-variant | CDC27 | GRCh38.p7 | 17:47188744 | CCGTAAACTTGCCCT[A/G]CCGTCACGAAGATCA | 996 |
rs376395370 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160176 | ATCCCTGGGAACATA[C/T]ATACTTGGAAAAATC | 996 |
rs376447814 | snp | C/T | 1.98124e-05 | 0.00314735 | intron-variant | CDC27 | GRCh38.p7 | 17:47181537 | TATTCATTTATCATT[C/T]TACAGCAATGAATAG | 996 |
rs376451975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155756 | AGGAGTTCCAGATCA[C/G]CTTGGGCAACACAGC | 996 |
rs376533878 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166454 | GGGTAGGTAGTGATA[C/T]TCCTTCTTTCATTCC | 996 |
rs376534443 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178445 | GAGGTTGAGGTGGGA[A/G]GATTGTTTGGGCCTG | 996 |
rs376553593 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141589 | TATTTTCAGACACAA[A/C]TGAATAGGACACACT | 996 |
rs376607788 | snp | A/T | 0.000103945 | 0.00720844 | intron-variant | CDC27 | GRCh38.p7 | 17:47156885 | ATTTGGTATTATAGC[A/T]CATTTGAAAGTATCT | 996 |
rs376627455 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141521 | CCCCAGTAATTAACT[C/T]TGTATATTGCAGAAA | 996 |
rs376633909 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141572 | TGGTAAATATAAATA[A/T]GTATTTTCAGACACA | 996 |
rs376654308 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134785 | GCCTTAATTGTTTTC[-/T]TTTTTTTTTTTTTTT | 996 |
rs376692733 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47160989 | AGCAGAAGTAGGATG[C/T]AGACTTTTGGAAAAC | 996 |
rs376699480 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178249 | TAAGGGTAAAAAAAA[-/A]TCTGGCCAGGCCACA | 996 |
rs376703073 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143605 | CTCCTAATAATCACT[-/G]ATCTGTTGTCCATTC | 996 |
rs376728637 | in-del | -/AT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166771 | ATCATAGTTTTTAAT[-/AT]GTCATATTTATTATC | 996 |
rs376796794 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131732 | GGAGTGCAGTATCAC[C/G]TTCTTAGCTCACAGC | 996 |
rs376818791 | snp | C/G | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157312 | ACTTGTGTTGTGCAA[C/G]AGTTGGGCAGACAGT | 996 |
rs376835265 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121816 | GTGATTTCGGCTCAC[G/T]GCAACTTCAGCCTCC | 996 |
rs376888011 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123296 | ATTGGCATATGGAGG[-/T]TCTAGTCTGTAAAAA | 996 |
rs376994143 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141185 | AAATTAAGCAAAAAA[C/T]GAATCATATCAACTT | 996 |
rs377001795 | in-del | -/GAAACCA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171678 | TCATTTAAGAAACCA[-/GAAACCA]ATAAGAATCGGTTAT | 996 |
rs377099882 | in-del | -/AAAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135704 | GAATAATCCTCCTTT[-/AAAC]AAACACAATTTTTGA | 996 |
rs377129069 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136966 | ATTATCATTAGTTAA[C/T]TTAAGAGTTTGTTAA | 996 |
rs377205142 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47174124 | ATAATGAAACTGTCA[A/G]ATAAGGAAGCAAATC | 996 |
rs377216741 | snp | C/T | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117524 | TTTCTACATCTTACT[C/T]CTTTCAGATCCTGAC | 996 |
rs377237963 | snp | A/G | 0.000125332 | 0.00791518 | intron-variant | CDC27 | GRCh38.p7 | 17:47181520 | TGGAATTTCATATAT[A/G]TTATTCATTTATCAT | 996 |
rs377249897 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158301 | GCAAGCCGATCTGTC[C/T]TGCTGTGGAGAGAAA | 996 |
rs377323844 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153893 | TTTGAGACCATCCCT[A/G]GCAACACAGTGAGAT | 996 |
rs377327023 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135002 | TAAATTATCTCATTT[A/C]ATCCCTAGAGGAATC | 996 |
rs377375611 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131754 | GCTCACAGCAGCCTT[C/G]CACTCCTGGGCTCAA | 996 |
rs377422212 | in-del | -/TAA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136870 | ACAAAGTAACAAAAC[-/TAA]ACAAACAAAAAACAA | 996 |
rs377467381 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124287 | TATCTATCTATCTAT[C/T]CATTTTTATTTATTG | 996 |
rs377472970 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174570 | CTCCATTAAGTCACT[C/T]TTAAAGTAATATTGA | 996 |
rs377519746 | snp | A/T | 0.000687561 | 0.0185286 | intron-variant | CDC27 | GRCh38.p7 | 17:47143991 | TGTTGTACTAAAAAA[A/T]AATTATAAAGGAAGA | 996 |
rs377526614 | snp | A/C | 1.66203e-05 | 0.00288268 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157059 | TGAATCAATATAAGA[A/C]ACTGAGGAATCTGTA | 996 |
rs377543231 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47124344 | GCTGGAGTGCAGTGG[C/T]GCCATCTCTGCTCTC | 996 |
rs377545958 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129638 | AAGGTTGTAGGGTCT[A/C]ACTGGATTGTCCACT | 996 |
rs377592568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47132169 | TCAACACAAAAAAGG[A/G]CCAATTTTTATCACA | 996 |
rs377692067 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131738 | CAGTATCACCTTCTT[A/G]GCTCACAGCAGCCTT | 996 |
rs377741647 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133058 | ACACACACACACATA[C/T]ATATACACACACACA | 996 |
rs386386174 | in-del | -/AAA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129996 | CTCAAAACTGTGTTA[-/AAA]ACACTCCTGTTTACA | 996 |
rs386386175 | in-del | -/TTTT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132096 | GCAATTCTGTGATTT[-/TTTT]TTTATGCTAAGCCAA | 996 |
rs386386176 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137812 | TCTCTCTCTTTTTTT[-/T]TTTTTTGAGATCTGG | 996 |
rs386386177 | in-del | -/AAGGA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175000 | AGGACAGGAAAGGAA[-/AAGGA]AGGAGAGAGAGAAAG | 996 |
rs386797411 | multinucleotide-polymorphism | CG/TA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136894 | AAAAAACAACTACAG[CG/TA]TCTGCAAAAGTTTGG | 996 |
rs386797413 | multinucleotide-polymorphism | AAT/CAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136964 | CTATTATCATTAGTT[AAT/CAC]TTAAGAGTTTGTTAA | 996 |
rs386797414 | multinucleotide-polymorphism | AAC/GAG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148099 | GCTACTCAGGAGGCT[AAC/GAG]GCAGGAGAATCGCTT | 996 |
rs386797415 | in-del | AAAG/GA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175028 | AAGAAAGAAAGAGAG[AAAG/GA]AGAGAGAGAGGAAGG | 996 |
rs397694830 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137818 | TCTTTTTTTTTTTTT[-/T]GAGATCTGGTCTTGT | 996 |
rs397701158 | in-del | -/CA | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47144893 | ACACACACACACACA[-/CA]TAAATCCTTTTAATC | 996 |
rs397737786 | in-del | -/A | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47163234 | AAAAGACAAAAAAAA[-/A]GTCTATACTGGAGAT | 996 |
rs397771464 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187860 | CAGAATAAAAAAAAA[-/A]TCTTAAAAGAAACTA | 996 |
rs397843912 | in-del | -/C | 0.0127383 | 0.0787839 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47188959 | CCGTGTTACCTCTGG[-/C]CCTACATTACTTCAC | 996 |
rs397954818 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175007 | GAAAGGAAAGGAGAG[-/G]AGAGAAAGAAAGAAA | 996 |
rs397977697 | in-del | -/TTTT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132099 | ATTCTGTGATTTTTT[-/TTTT]ATGCTAAGCCAAATG | 996 |
rs527236360 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47137446 | AAATCAAGCCTCAAC[G/T]TAGAACAGAAAGACA | 996 |
rs527282124 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140276 | TGCCACCACACCCAG[C/G]TAATTTTTTCATTTT | 996 |
rs527290409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47130263 | CTACTTGGGAGGCTG[A/G]GGCAGGAGAATTGCT | 996 |
rs527301622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47136774 | TTTTCCTATTATCCA[A/G]TAAGTGAATTATGCT | 996 |
rs527332471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178064 | AATACATGCTTACAA[C/T]GGGGGAAGGGAATTT | 996 |
rs527395037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47177123 | TAGAAAATTGGTGAA[C/T]GATTTTACGGTCATT | 996 |
rs527397214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47123215 | ACTGCTTAATTAACT[G/T]TCATTTACAGTGATT | 996 |
rs527397359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47130987 | GAATAGGTAGTGCCA[A/G]CGTCTGCTTGCTAAA | 996 |
rs527415980 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181996 | TTTCCTGGCTGATGT[A/C]AAGCCATTTCTTTTT | 996 |
rs527483236 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47150742 | ACAAAATTATTAAGA[C/G]TGAATGTTGGCCAGG | 996 |
rs527485204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159538 | CTTGCAAGGGACGGC[A/G]TAGGGCTTGCCAATC | 996 |
rs527550885 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142824 | ACTGAGATTACAGGC[A/G]TGAGCCACCACGCCC | 996 |
rs527630769 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124580 | TGAGCCACCATGCCC[A/G]GCCCAGTGATTTATT | 996 |
rs527631273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155168 | TAACTATAACTCTCC[A/G]GAGTTGTAATCTCAT | 996 |
rs527654174 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47188108 | ATTTACTGTTTGATA[A/C/T]CTCAAGCCTTTTAAG | 996 |
rs527713348 | snp | A/C | 4.19842e-05 | 0.00458152 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120908 | CACTAGTCACACATC[A/C]AGTTGTAAAAGTCTG | 996 |
rs527792960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47184221 | GTTTATTTATTGGAG[C/T]TGTTTTGTGGATTAA | 996 |
rs527832683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135401 | AGACTTCTCATGGCC[A/G]TAACTAGATGATGAT | 996 |
rs527892869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47142685 | TAGCCCTCTTGTGAA[A/G]GTATATCAAACTCTC | 996 |
rs527941248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175247 | AAACAGAAAGGTAAA[C/T]TAGTCTTTCAAAGCT | 996 |
rs527948231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47142804 | CTGCTTCAGCCTCCC[A/G]CGTAACTGAGATTAC | 996 |
rs528005515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128529 | CTAGAACTAGTCTCC[A/G]TGTTATAAGCTCTCA | 996 |
rs528020408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158785 | CACCATATCCGGCTA[A/G]TTTTTGCATATTTTG | 996 |
rs528069469 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47163982 | TTGGCCAGGCTAGTC[A/T]CGAACTCTTGACCTC | 996 |
rs528097088 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118868 | GCGGAAACTGTCCCC[C/T]AACCAGCCATTGCCA | 996 |
rs528116783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47162924 | GAGCTAACTAGGGAA[C/G]AAGTCAGGTGTGGAA | 996 |
rs528143416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164704 | CACATGTAATCCCAG[A/C]TACTCCGGAGGCTGA | 996 |
rs528229881 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146629 | TGGGACAAGATTAGT[C/T]CAGACTAAGGCTACT | 996 |
rs528286308 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47132574 | TTTTTAAATAAAAAA[A/T]TTTTTTTTTGAATTA | 996 |
rs528295860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47188536 | CCCTTTCCACCTCCT[C/G]CCCTGGTATTGGTGC | 996 |
rs528296432 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125967 | GTTATCAACATTTCA[C/T]GCAACCAGCATGCCT | 996 |
rs528309629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132017 | CCTATGAGGTAAGCA[A/C]GTAGTACATGACATT | 996 |
rs528327756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47170683 | AGAAGGAACAGAAGA[C/T]GATTACTATACTGGG | 996 |
rs528468043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47153089 | TGGGATCACTACATT[C/T]ATCCAAGGGACAAAA | 996 |
rs528659431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160472 | CTCAAGTGATCCACC[C/T]GCTTCAGCCTCCCAA | 996 |
rs528666240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47169502 | ATACAAAAATTAGCT[A/G]GGCGTGGTGTCGGGC | 996 |
rs528716921 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168880 | GCTATCCTAGTTCTT[A/T]AGACAAGCAGTCCCC | 996 |
rs528746312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47161380 | AAGAAAGGGCATACA[A/C]AAAAACATTTGCTGA | 996 |
rs528818255 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171106 | CTTTCTCTAAAAAAA[G/T]GAAAAAAGAAAAAGG | 996 |
rs528852120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47150384 | CTGGGTTGACCCTAA[C/T]CCAATATAACTGTTG | 996 |
rs528864486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47149626 | AGAAATTGTAGTTAT[A/G]TGTGTAAATATAAAA | 996 |
rs528982299 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47143187 | CAGGCTGGTCTCAAA[A/C]TCCTAAGCTCAAGTG | 996 |
rs529012454 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146748 | TACCTAAAGGAATGC[-/A]AAAAATATCCAGTAA | 996 |
rs529040551 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120788 | TCATTCTGTATACAG[A/T]CAGGGTCCAATGAAA | 996 |
rs529055184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166386 | AAGTTGTTAAATTCA[C/T]GTGCATAGAGTTGTT | 996 |
rs529064011 | snp | G/T | 0 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157380 | GTCAGGATCTGGCTT[G/T]TCACCTGTGAAGACA | 996 |
rs529142903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158121 | CTTGGGGGTAGATGA[C/T]CTGTATTGCTCTCCA | 996 |
rs529176028 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172163 | AAAAAAAAAATTAGG[C/G]TTGCTATTTTAACAC | 996 |
rs529193778 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47179380 | TTGGTTCAGTGGGAA[C/T]GAGTACTGTAATGGA | 996 |
rs529233246 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130555 | TAATATTCTGCTATG[C/T]TCCTCCTTGGACAAA | 996 |
rs529239400 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176484 | TTAAAACCACGCTTA[C/G]AGTAAAAAGACCACA | 996 |
rs529246195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127334 | TCTTCATAAAGAAGA[C/T]AGAATAAAACTAAAG | 996 |
rs529269307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134711 | GATCTCTTGACCTCA[C/T]GATTCGCCCATCTCA | 996 |
rs529321284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47141526 | GTAATTAACTCTGTA[C/T]ATTGCAGAAAAATAA | 996 |
rs529321902 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120121 | TTATTAAGGGCCTTG[C/T]TTTGGCTTCTCAGTG | 996 |
rs529322277 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47134347 | TCTTGCTCTGTCGCC[C/T]GGGCTGGAGTGCAAT | 996 |
rs529470312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156104 | TTTTAATGTGTTTAC[C/T]ACCTAATTAAGGAAT | 996 |
rs529501879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148190 | GGCAACAGAGCGAGA[C/T]TCTATCTCAAAAAAA | 996 |
rs529514519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147743 | CAAAAAAATAAAAAA[C/T]AAAAATAATCAGCCA | 996 |
rs529593096 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139853 | TTTTTTTCCTCATCA[A/C]ATTCACAGCTCCCAG | 996 |
rs529643557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47141266 | TTTTTTTAAGTTGGG[A/G]GTGGAGAAAATGCTT | 996 |
rs529652325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124053 | CCCAAATCATCTTCA[C/T]AAAAGCTAACTAAAT | 996 |
rs529672180 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171754 | CAATGAAATCTCCAT[A/G]ATATAAATAATGCCA | 996 |
rs529689242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47131240 | TGAATTGAATAAATA[A/G]GGTGATGACAACAAA | 996 |
rs529727842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47187394 | CAAACTCCATCTCCT[A/G]GGTTCAGGCAATTCT | 996 |
rs529752253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47178205 | CAACAAAACCACTCA[A/G]TGGAAAATATTAGAG | 996 |
rs529802730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124655 | TTATTGAGAAGAGTG[G/T]CATTAACATTTTTGC | 996 |
rs529836616 | in-del | -/T | 0.337841 | 0.23406 | intron-variant | CDC27 | GRCh38.p7 | 17:47158621 | CAGTATTATTCTTAA[-/T]TTTTTTTTTTTTTTT | 996 |
rs529859642 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168146 | TTCACTACATAGGCA[C/T]TACTGATTAAACCAT | 996 |
rs530083170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168124 | CCTTTTGAGTTTTTA[C/T]GGAGGCTTCACTACA | 996 |
rs530100609 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153863 | CAAGGCAGGAGGATT[G/T]CTTGAGCCCAGGAGT | 996 |
rs530163268 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159639 | TGGCAGTGGCCACCT[C/T]CTTGGAGCATTTAAC | 996 |
rs530178092 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133279 | AGTAGCTGGGGATTA[A/C]AGGCATGCACCATCA | 996 |
rs530198930 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160377 | GGATTACAGGTGCAC[A/G]CCACCATGCCAGCTA | 996 |
rs530227699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47129161 | GATGAAAAAACTGCC[C/T]TTCTATATAAGACAT | 996 |
rs530248230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136035 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 996 |
rs530283633 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124790 | CCATTTGGACAGAAT[C/G]AGAGTGAAAAAGGTA | 996 |
rs530289781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47167417 | CTCTCAAATAATTTG[C/T]AGTCTTTGAACATCT | 996 |
rs530289822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176865 | ATTCCACATCTTTAG[A/T]AGAATTCTGGATATT | 996 |
rs530348867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176036 | ACCTACCTTTAAAGG[C/T]TGCTGTTAGGATTAA | 996 |
rs530388040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47123064 | TCCTACAGATGAACT[C/T]ATACCAGCTTTTGAG | 996 |
rs530425315 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47122177 | AGATAAAACAGTACT[A/G]GTTACATATTCAAAC | 996 |
rs530432117 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47130162 | GTCAGGAGATCGAGA[A/C]CATCCTGGCTAACAC | 996 |
rs530447094 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47185248 | CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC | 996 |
rs530467707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164771 | GCAGTGAGCTGAGAT[G/T]GTGCAACTGTACTCC | 996 |
rs530492539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156799 | AAACAGAATGCCCCT[C/G]TTTCCACAGTGATTT | 996 |
rs530508113 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172147 | ATAAACAAGTTTAGC[-/A]AAAAAAAAAATTAGG | 996 |
rs530508270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156175 | ATGGAGTCTTGCCCT[A/G]TCTCCCAGGCTGGAG | 996 |
rs530558979 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47164552 | TGGACACGGTGGCTC[-/A]ATGACTGTAATCCCA | 996 |
rs530674249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164016 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAATGCT | 996 |
rs530687329 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119036 | CTCCAGGCTTTATAA[C/T]GCAGAACTCAGGTTG | 996 |
rs530737560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172399 | GATCTTGTTTTTAGG[C/T]AATATTTTTCTAATA | 996 |
rs530738805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47181069 | CCAGCCTGGGCAACA[C/T]AGCAAAACCCTATCT | 996 |
rs530809144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47139518 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 996 |
rs530813509 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128961 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 996 |
rs530821131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147171 | TTTGGGAGGCCGAGA[C/T]GGGCGGATCACGAGG | 996 |
rs530884287 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165612 | ATTTTCTCCCAGGCT[A/G]TGACTTGTGTGTATT | 996 |
rs530916753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47188637 | AAGGAAACGTGGGAT[A/G]GGAAGTCTGTTACCA | 996 |
rs530926948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132642 | CCAATCATAGCTCAC[C/T]GCATCCTTGAACTTC | 996 |
rs530943763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140363 | AAGTGATCCCCCTTC[C/T]TTGGCCTCCCAAAGT | 996 |
rs531029796 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CDC27 | GRCh38.p7 | 17:47189320 | GTGCTTCCGAGCGGG[A/T]CACGGGAATACCCGA | 996 |
rs531031150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47135396 | TACGGAGACTTCTCA[C/T]GGCCATAACTAGATG | 996 |
rs531057298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47161548 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 996 |
rs531092795 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167134 | GGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 996 |
rs531117424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47162447 | CTCTCTGAGAATGGA[A/G]AATTAGTCTTTGCCA | 996 |
rs531178736 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47170284 | GTTCACATGGCCTCA[A/T]ATTCCTGGACTCAGG | 996 |
rs531197141 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47146934 | AGCCATATGTGGCAC[A/G/T]TGCCTATAGTTCCAG | 996 |
rs531203438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136055 | GCTGAGGCAGGAGAA[C/T]GGCGTGAACCTGGGA | 996 |
rs531216224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143236 | CCCAAAGTGCTAGGA[G/T]TACAGGCGTGAGCCA | 996 |
rs531224184 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186909 | AATCTGTCATCATAG[-/T]TTTTTTTTTAATAAA | 996 |
rs531301393 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47185272 | CAAGCTCCACCTCCT[C/G]GGTTCACGCCATTCT | 996 |
rs531476741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47150518 | GGGGTTATCAGAAGC[C/T]GGAGGAGGCAAGGAA | 996 |
rs531479066 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137549 | GCTAAAATTTATTTG[C/T]AAAACCAAAATCAAT | 996 |
rs531516887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158954 | ATGGGGTTTTGCCAT[A/G]TTGCCCAGGCAGGTC | 996 |
rs531520491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47149755 | AGGTCAGGAGTTTGA[C/T]GCTAGCCTGGCCAAC | 996 |
rs531600471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128357 | TTAAAAGATTTTGCT[C/T]CATGGTTTCTGATTG | 996 |
rs531631945 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165704 | TTTTATGTACTGTCA[C/T]TTGGGTGTTATGTTT | 996 |
rs531715934 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120823 | CACACTCATGGTATA[A/T]GTGACGGACGATGAC | 996 |
rs531722916 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120352 | GATATTTGATTCCTA[C/T]ATACGAGTCCCAATA | 996 |
rs531732384 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47175135 | AGTTCCTCTTCTTAC[A/C]AACAGGTTTGGCTTC | 996 |
rs531759472 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159712 | CGCCTCGAACCTGGT[A/G]CCCTGGCTGGCACGG | 996 |
rs531764709 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CDC27 | GRCh38.p7 | 17:47174593 | AATATTGAGAAATCA[A/G]TCGTGTACTAGTTAA | 996 |
rs531936233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141696 | TAACACAAGAAAGAA[C/T]TATATCTATAAATTA | 996 |
rs531950366 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141272 | TAAGTTGGGGGTGGA[G/T]AAAATGCTTTGGGAA | 996 |
rs532026413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47182459 | AAAACCTCTCCCTGC[C/T]CCAAAGAGGAAACCA | 996 |
rs532204853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47162808 | TATAATGAGTAATTA[C/T]TTCATGAATAGACCA | 996 |
rs532261019 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47178946 | TGGCTGGGATTACAG[G/T]CATGTGCCACTACAC | 996 |
rs532346155 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47146223 | ATTAAGTATAGCACT[C/T]TCCTGGACTCTGTGA | 996 |
rs532357338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47137729 | CTGGGGACAGTTGGA[C/T]AGAATTTGAATCCCA | 996 |
rs532383207 | in-del | -/AAAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147401 | GAAACTCCGTCTCAA[-/AAAC]AAACAAACAAACAAA | 996 |
rs532390264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152383 | TTCTAAAGGAGTTCA[C/G]AGGAGTAGATTTTAA | 996 |
rs532472716 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47145677 | GCAGGCCAAGGCAGG[C/T]GGATCACGAGGTCAA | 996 |
rs532498880 | snp | A/G | 3.32657e-05 | 0.0040782 | intron-variant | CDC27 | GRCh38.p7 | 17:47129527 | CATGTTGAACCTGTA[A/G]GAAATAAAGATCATG | 996 |
rs532536622 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159864 | TGATCTTCATGTCCT[G/T]GACCAGGAGCCCCAG | 996 |
rs532612913 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156593 | GCTGGGATTACAGGC[A/G]CCCGCCACCATGCCC | 996 |
rs532627587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159604 | CGAGAGTTTGGCCAG[A/G]ATGTTGATGGCCCTG | 996 |
rs532631001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47177008 | GAAACAGATGCTGAA[C/T]GTTTTACTCTGGTTC | 996 |
rs532687704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168220 | TAATCTTCAGCTCCT[C/T]TCACCTCCTGGGAGG | 996 |
rs532791623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176785 | GATGTGTCTGTGAAA[A/C]ATCCAAGTTAATTCA | 996 |
rs532847091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47123875 | TTTGGGACCATGACC[A/C]CAGTCTTTACCTTTC | 996 |
rs532859513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47177921 | TTGCATTAATGTATT[A/T]TTTTCCTCATAGTCT | 996 |
rs532939068 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47164807 | GAGCGACAGAGCGCA[A/G]GATTCCATTTCAAAC | 996 |
rs532973044 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47122282 | CTCATTATCTGACTT[-/TA]TATGCATTTTGTTAT | 996 |
rs532987695 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127274 | AAAAACTAAAGAAAG[A/T]CAAGCTTTTTAAAAG | 996 |
rs533022716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156284 | GCTGGATCTACAGGC[A/G]CGTGCCACCACACCC | 996 |
rs533042703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47165567 | TATATAGTCTAGATA[A/C]AATCTGTGTTGTTTA | 996 |
rs533076916 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119954 | ACTCTGCTTAAGCAA[A/G]CACTTAGAAAAGTCA | 996 |
rs533125162 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47187737 | AACTATTAAAACAAA[A/G]TTATAAGAATATGCA | 996 |
rs533170845 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47141096 | ATTGTCTGACTAGCT[C/G]TAATACAGAGTCTAG | 996 |
rs533195678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47173771 | GTTCAAATGGGAATA[C/T]GGATTGGTGATTTAG | 996 |
rs533241852 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183036 | AAAACACAAAAAAGA[A/C]TCTCTCCAAATTAGG | 996 |
rs533264191 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47126656 | ATTAAAATGGCTTTA[A/C]GAATAATGAATAAAG | 996 |
rs533284293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47180449 | TAAGGCTGGTTTCCA[C/T]TTAACTTCTCAAAAC | 996 |
rs533306893 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149156 | TAAAGATGAAATAAG[A/C]ACTTTTTTTCTGATC | 996 |
rs533350392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147269 | CTGGGCATGGTGGCG[C/T]GCGCCTGTAGTCCCA | 996 |
rs533374385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140503 | AAGTTTTCAGAATCT[G/T]TTGCTTCCTCTGAAA | 996 |
rs533375903 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139412 | GCTGGGACTACAGGC[A/G]CCTGCCACCACACCT | 996 |
rs533497111 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187988 | TTCAAACACTAATAG[C/T]TGCTATATGTAAACA | 996 |
rs533552177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155315 | CAGTGGCATGATCTC[A/G]GCTCACTGCAACCTC | 996 |
rs533651444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47147618 | TGGCTCATGCCTGTC[A/G]GCCCAGCACTTTGGG | 996 |
rs533709313 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47135650 | TAGTTACCTAAATAC[A/G]TCAGCATTTAAACTC | 996 |
rs533750762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47142805 | TGCTTCAGCCTCCCG[C/T]GTAACTGAGATTACA | 996 |
rs533835833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168251 | TTGCGGGGTGGGGAT[A/G]AAAAGTCCCAATCCT | 996 |
rs533857053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128894 | TCCTGCCTCAGCCTC[C/T]CCAGTAGCTGAGACT | 996 |
rs534149499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47182655 | GTTTTGAAAATTCAT[C/T]CTTGATGTGTGTAGC | 996 |
rs534159532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158518 | TACAAAACAAACTAT[C/G]GTTGCCTTCTTGAAT | 996 |
rs534166769 | snp | C/G | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117728 | CATAGTATTTATTTT[C/G]ATATTCCAAATAATA | 996 |
rs534183410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47166019 | AATTACTGGCTCAAA[C/T]AGTAATTCTAGTTTC | 996 |
rs534188574 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141430 | CTTGTATTAAAGACA[C/T]TGTGTCCTCAATTCA | 996 |
rs534205473 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118532 | GTGCAAAAGTAATTG[A/C]AGGTTTTGCCATAAA | 996 |
rs534224251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47157616 | ACAAGAACACTAATT[A/T]TAAACATAACAAATC | 996 |
rs534306023 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147268 | GCTGGGCATGGTGGC[A/G]CGCGCCTGTAGTCCC | 996 |
rs534402159 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119611 | AATTTCTCTAAAAAT[G/T]TCAATACATTACAGT | 996 |
rs534429774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174142 | AAGGAAGCAAATCCA[C/G]AGCAATCTGAAGTGT | 996 |
rs534431240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47127487 | AACTCACTGCAACCT[C/T]TGCCTTCCAGTTTCA | 996 |
rs534525109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164981 | CCCAAAGAAACCCCT[A/G]AATAGTTACATCCTC | 996 |
rs534535986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178989 | TATTTTTTAGTAGAG[A/G]TGGGGTTTCTCCATG | 996 |
rs534628978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160940 | TTCCCACACTTGTGT[A/G]ATTTAAGCCAATAAA | 996 |
rs534646408 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47153328 | TAACTTGCTCTGGTT[A/C]TTATGGTTATTATGG | 996 |
rs534672258 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47186040 | GCCCCAAATGTCAAT[A/G]GTGCTCAGATTAAGC | 996 |
rs534672489 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CDC27 | GRCh38.p7 | 17:47147338 | CGGGAGGCGGAGCTT[A/G]CAGTGAGTCGAGATC | 996 |
rs534711882 | snp | C/G | 3.29783e-05 | 0.00406055 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137264 | GAGTATAGGCATAAG[C/G]GTAATTTGGATCAAC | 996 |
rs534781567 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140102 | AAAACTGAGTGCTTA[A/C]TTCCAAGAAGTGGTC | 996 |
rs534782594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178378 | TCGTGTTCTCAAAAA[C/T]ACAAAAATTAGCTGG | 996 |
rs534810291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47125090 | TGCCTAATTTTGTTT[C/T]GTATTTTTAGTAGAG | 996 |
rs534870089 | snp | A/G | 1.78886e-05 | 0.00299065 | intron-variant | CDC27 | GRCh38.p7 | 17:47151984 | ATGATAAAAGACAAC[A/G]CAACGCTCCCATCTA | 996 |
rs534922344 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172774 | GTCTATGTCTCTACT[A/G]AACTGATCATCACTT | 996 |
rs534929769 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47151028 | CAAGAGTGAAACTCC[A/G]TCTCCATAAAAAAAA | 996 |
rs534932439 | snp | A/T | 1.66796e-05 | 0.00288782 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169928 | TTACCAATATACATG[A/T]CCCAACAATGAAAGA | 996 |
rs534953521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145053 | TCATCTCTAAAAAAA[C/T]TTTCTAAATAGAAAG | 996 |
rs534975144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47130624 | TCACGCCTGTAATCC[C/G]AGCACTTTGGGAGGC | 996 |
rs535007853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47137844 | CTTGTTCTGTTGTCC[A/G]GGCTGGAGGGCAGTG | 996 |
rs535068427 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47183144 | TTAGTAATAAACTAC[-/T]TTTGAGATATCTCAC | 996 |
rs535216712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128180 | GGTCTACAGGTGCAC[A/C]CCACCATGCCTGGCT | 996 |
rs535310341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47148021 | TGACCAACATGGTGA[A/G]ACCCCATCTCTACTA | 996 |
rs535332127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156311 | ACCCGGCTAGTTTTT[G/T]GTATTTTTAGTAGAG | 996 |
rs535332923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148988 | GGAGGCCGTGGCAGG[A/G]GAATTGCTTGAACTC | 996 |
rs535347493 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176558 | TTGAGGCAGAAAATG[A/G]CAATATATGAGGAGA | 996 |
rs535347634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140979 | CTCCCAGTTTCCTCA[C/T]CATGCTTCATTTTTC | 996 |
rs535386899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127522 | ATTCTCCTGCCTCAG[A/C]CTCCCAGGTAGCTGG | 996 |
rs535444092 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122108 | TCTAATCAGAATTTA[C/T]CTTGTCAGAAATTTC | 996 |
rs535488081 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117606 | AGAAATTTCAGAAAT[C/T]ACGTGATCAAAGAAT | 996 |
rs535532986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164888 | TAGCAGTTTTTACAC[A/G]TTTATATAGAGAATA | 996 |
rs535536109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47183798 | TTTAAAGCAGGTGCT[G/T]ATATGTTGAATGAAT | 996 |
rs535582634 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162345 | CATCCCTTCAATTCA[A/T]CTATCTAGGCCCCTT | 996 |
rs535724915 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191024 | GACCTCTCTTTTCAC[A/T]CTGGCCTCTTATGAG | 996 |
rs535784582 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189582 | TGGGCGTGGCGTGAC[A/G]GCGCGGGCGGGTAGC | 996 |
rs535794272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47133754 | TGGCCTACATATATT[A/T]TTTTTCTTTTTTGAG | 996 |
rs535900704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155692 | GGTTCAGTGGCTCAC[A/G]GTAATCCTAGCACTT | 996 |
rs535924153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47152026 | TACAAGCAGCCATAA[C/T]ATACTGTCACCTTAA | 996 |
rs535965560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47164264 | GTGCATATGCACTTT[A/G]TGATGTTCACAAATG | 996 |
rs536040522 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151445 | ATTCATTATTTGAAG[G/T]TTATTTGTCTGTTAT | 996 |
rs536135935 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47148385 | TCCAAAATGAAACAC[A/G]GAGAGGAGAAAGATT | 996 |
rs536153857 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47180640 | TGTACACAATGATCT[A/G]TATCAGCATCTTAGA | 996 |
rs536153873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47171313 | ACTTACTTGTATCTT[C/T]CCCTTGTAAACCTAC | 996 |
rs536172892 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175291 | GACGCCTCTTCTTCA[C/T]GCTGATTTATAATCT | 996 |
rs536202280 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137376 | CTTAAAAAAATGGGA[A/G]CAAAAACCAAACAGA | 996 |
rs536302309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160609 | CAGGTAAAAAATACA[A/C]CTTACCTGGTCTGAA | 996 |
rs536328370 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47166769 | ACATCATAGTTTTTA[-/AT]ATGTCATATTTATTA | 996 |
rs536376805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47169023 | TGGAAACAGGGTCTC[A/G]CTCTGTTACCCAGGC | 996 |
rs536414051 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127612 | TTCACCAAGTTGGCC[A/G]GGCTGGCCTCAAACT | 996 |
rs536422826 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162592 | TGTATGAATTATTTA[C/T]ATGGCCAGAAAGGAA | 996 |
rs536457799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136207 | GAGAACATAGCTATC[A/G]GAAGAGACAGCAGCA | 996 |
rs536503504 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47158642 | TTTTTTTTTTTGGAC[A/C]AGGTCTGGCTCTATC | 996 |
rs536543231 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47154090 | CGAGACCCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 996 |
rs536567281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47130347 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 996 |
rs536571073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47166688 | TGAAAGCTTAGATAG[C/T]AGAGTTGAAACTGTT | 996 |
rs536644844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179040 | TTCCCAACCTCAGGT[A/G]ATCTGCCCACCTCAG | 996 |
rs536714438 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47143659 | TATTCCTATGTCATT[C/T]TTAACTTGAGAAAAA | 996 |
rs536879516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47125876 | CTAAGATGACACACT[C/T]CAATCCTCCTTCACT | 996 |
rs536880298 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120456 | TTATAGGCAACGTCT[C/T]TTATTGTTCCATCTG | 996 |
rs536882688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166090 | ACATCTGATTTCCTA[A/T]TTTTTTTTGAAGATT | 996 |
rs536884555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128639 | GAGTACTAGATAGTA[A/G]GCCCCTCAAAAGCAG | 996 |
rs536972282 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47163070 | TTATTAAAATTGAGT[G/T]ATACACACAAAACCC | 996 |
rs536994001 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | CDC27 | GRCh38.p7 | 17:47154049 | AGTCATGGTCACACC[A/C]CTGCACTCCAGCCTG | 996 |
rs536997058 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125703 | CGCCCGCCACCATGC[C/T]TGGCTAATTTTTGTA | 996 |
rs537028846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47139912 | AGGATTTAGGTTATA[G/T]AAAATCAGTTTCCTA | 996 |
rs537091246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47131635 | AAAGCAAACAAACAT[A/T]ATGTACATATCTTTT | 996 |
rs537098628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147378 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAAACTCC | 996 |
rs537130421 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137638 | GACTCTACCTTCTTG[C/T]TTTAGCTCTCATGCA | 996 |
rs537191948 | in-del | -/ATA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140025 | TTCACAGTTTAGTTT[-/ATA]ATAAGGAATATCTGG | 996 |
rs537224804 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168562 | TATCTTTATATTCAA[A/G]CCAAGTGTGTTTAGC | 996 |
rs537232547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145856 | GAGCCAAGATCGTGC[A/C]ATTGCATTGCAGCCT | 996 |
rs537319386 | snp | C/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47137987 | TGTATTTTTTGTGGA[C/G]AAGGGTTTTGCCATG | 996 |
rs537407555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132132 | TAGTATTTTTGGGTG[A/T]AATAGGCTCCAGAAT | 996 |
rs537415568 | in-del | -/ACT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164531 | AGTACAAAACTGTAA[-/ACT]ACGCTGGACACGGTG | 996 |
rs537422419 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157870 | TGTAAGTTTCAGGCA[C/T]TTATTAATTGCATTA | 996 |
rs537423734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47187888 | CTATACTGGTAAAAA[C/G]AATTTGGATGGAAAT | 996 |
rs537488558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135599 | AACAAAAGAAAGGCT[A/G]TCTATTTTGTACTTA | 996 |
rs537492291 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47167921 | GGGATTCCCACAATG[-/C]TCTATTCAGGTTTGA | 996 |
rs537500961 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47166762 | TTTAGCAACATCATA[C/G]TTTTTAATATGTCAT | 996 |
rs537511290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140927 | AGAGTAACCTTCCCT[C/G]TGAGTACATAAAAAC | 996 |
rs537557384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47121320 | GAGACATTAAAAAAA[A/C]AAAATTGACATTTCC | 996 |
rs537694519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152560 | TATTCCCTTATTTCT[A/G]TTCATTTCCACCATC | 996 |
rs537696348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47149092 | CAAAAAAAAAAAAAA[A/G]AAAAGAAAAAGAAAG | 996 |
rs537886931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128228 | TAGAGATGGGGTTTC[A/G]CCCTGTTGGCCAGGC | 996 |
rs537914509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47157469 | AAATCAGTGGAAACA[A/G]GAAATAGGCCTTATC | 996 |
rs537942027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47176208 | TGTCCCTGAGCCACA[C/T]GCTCAAGTAATTCTA | 996 |
rs537950659 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123437 | TCTTTCTGAGACAGA[A/G]TCTTGTTCTCTTGCC | 996 |
rs537990668 | snp | C/G | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157285 | TGTCTGTGAGATAAA[C/G]TATGATTAGGTACTT | 996 |
rs538024109 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190515 | TCATGATATATTCCA[C/T]TGCTTGGAAATTTCC | 996 |
rs538028807 | in-del | -/GA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175050 | GAGAGAGGAAGGAAG[-/GA]AGGAAGGAAGGAAGG | 996 |
rs538172666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127410 | TTAGCCTATTTTTAC[A/G]TTTTTTTTTGAGATG | 996 |
rs538195565 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124824 | AACGTCAAGATATTA[C/T]TGTAAAAATAGCTTT | 996 |
rs538221591 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131296 | CTCTCCATTTTTTCC[A/G]TAGTAGCTAACTATA | 996 |
rs538299318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148507 | ATGGACATAATATTT[A/G]AAGAAATAATGCCCC | 996 |
rs538319107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145924 | AGTCAACCATGTGAT[C/T]AGAGGGCTGGGGCTT | 996 |
rs538326442 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149781 | CCAACATCGTGAAAC[A/C]CTGTCTCTACTAAAA | 996 |
rs538357782 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161142 | GATTCTCCTGCCTCA[A/G]CCTCCCAAGTAGCTG | 996 |
rs538358528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156360 | GGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 996 |
rs538372534 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146397 | AACCTGTGGTGTCTG[C/T]GCTAAGTTTGGGTAG | 996 |
rs538383199 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121589 | CTGGGACTATAGACA[C/T]GTACCACCACAGCCA | 996 |
rs538390919 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47126897 | CTCATGGGTTCAAGC[A/G]ATTCTCATGCCTCAG | 996 |
rs538391363 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145641 | GGCATGGTGGCTCAC[A/G]CATGTAATCCCAGCA | 996 |
rs538395763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134384 | ATCATAGCTCACTGC[A/G]GGTAACCTTGAACTC | 996 |
rs538405488 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47123647 | AAACTCCTGACCTCA[C/T]GTAATCTACCTGCCT | 996 |
rs538451382 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47147208 | GATCGAGACCATCCT[C/G]GCTAACACGGTGAAA | 996 |
rs538477194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47186878 | AACTTACTCTCATTG[C/T]TTTCCAAATACACGC | 996 |
rs538535112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174081 | CCTGGGTGACAGAGT[A/G]AGATTCTGTTTAAAT | 996 |
rs538547174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172991 | GCTAGAAATGAAAAT[G/T]TTTGTGTCCCATCTC | 996 |
rs538574836 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47168402 | GAGGAAATGAGGTCA[A/T]AGACCAAATATATAT | 996 |
rs538592638 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165375 | TCAGTAGTTTTTATT[C/T]TTAGCCATTGTATCT | 996 |
rs538616317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47161706 | AGTGAGTCGAGATCA[C/T]GCCATTGCACTCCAG | 996 |
rs538616382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152634 | TTTTCCCCTTTGGCT[A/G]CCAGAGAATTTTCTT | 996 |
rs538701837 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47153226 | TTCTGGGAATGTCTT[G/T]TAATAAGGTAAGAGG | 996 |
rs538706011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143734 | GACTAATTAACTTCA[C/T]AAAAATCATAGATGG | 996 |
rs538737693 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47185788 | AAAAAAATCACTGTT[A/G]AAATTTCATATTATA | 996 |
rs538741442 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167760 | GCCAGCTGAATGTCC[A/G]CTAATTCAATTCTGA | 996 |
rs538874201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47130454 | CTCTAATACTGGGAA[A/G]CAAATAACTTAAGAT | 996 |
rs538880135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47167589 | ATTTTATGACAGAAC[A/G]TTTAATGTGATAATA | 996 |
rs538886230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47158766 | TGAGACTATAGGTGC[A/G]CACCACCATATCCGG | 996 |
rs538938544 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47124202 | ACACACACACACACA[A/C]ACACACACCCCTCTT | 996 |
rs538940278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178292 | TGTAATCCCAGCACT[C/T]TGGGAGACGGAGGTG | 996 |
rs538968689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159229 | CCCGGGTCCTCTGTA[C/T]GGAGACTCTAGTGTG | 996 |
rs539010062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47144808 | AGATATATATTTTCA[C/T]CTTTTACGATATGTA | 996 |
rs539051524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141334 | AATTTTCTTTGGCTT[C/T]AGGTTAATCATTCTC | 996 |
rs539063430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148328 | TAACAGGTCTGACAC[C/T]GCTGAAGAAACATTA | 996 |
rs539104146 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148890 | TCAAGACTAGCCTGG[C/T]CAACATGGTGAAAGC | 996 |
rs539109496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136991 | TGTTAAAGACGTACA[C/T]TTCATAAGAAAACAT | 996 |
rs539111723 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125183 | CCTTGGCCTCCCAAA[A/G]TGCTAGGATTACAGT | 996 |
rs539135956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47181776 | GCCCACAGAGCAAAC[A/T]CCAGAGTGTGCCGGG | 996 |
rs539222058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155606 | CCTCTGGGCTGAGTT[C/T]CTGTATTTATACATA | 996 |
rs539308568 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184846 | AATCAGCACCTCTGC[C/T]CAACTGATGGTGTGG | 996 |
rs539320645 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149950 | ACAGAGCGAAACTCC[A/G]TCTAAAACAAAAACA | 996 |
rs539411633 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145343 | CAGAGAGAAGAGAGC[C/T]ACAAAGAGGAGACCT | 996 |
rs539415001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179556 | TAGGATTATTGAAGA[C/T]TAAATTAGTAACTAA | 996 |
rs539420136 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47140818 | TCTGTTCTGTACTAT[A/T]CAAAATTAAATTATA | 996 |
rs539486959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132892 | AATCCTCCCACCTCA[G/T]CATCCTGAGTAGCTG | 996 |
rs539499391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47163249 | AGTCTATACTGGAGA[C/T]AGAAAAGAAAACCTA | 996 |
rs539504862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172505 | GAAATAATTTCTATA[C/T]TTTAAAAAGACCAGA | 996 |
rs539727567 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137524 | TCCATATTTGTGAAT[C/T]TGTCTGATTGCTAAA | 996 |
rs539804101 | snp | A/G | 0.000593718 | 0.0172194 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138852 | TGCCTTCAACTCTAT[A/G]ATTCTCAATCCTTCT | 996 |
rs539851451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179702 | TTCCTCATATAAATA[C/T]GGTTAAACCGAATGG | 996 |
rs539894518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47150276 | TGTACCTCCCCAAAA[A/G]ATATGTTGAAGCCCT | 996 |
rs539936474 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181951 | CTCGTCCCTAAAGAT[A/C]CAGCTTAAATAACAT | 996 |
rs539940160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47170981 | TGACACGTGTCTGCA[A/G]CTCCAGCTACGTGGG | 996 |
rs539956830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158820 | GACCAGGCTTCACCA[C/T]TGATGCCCAGGCGGG | 996 |
rs539998925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128316 | GATTACAGGTGTGAG[C/G]CACTGCGCCCAGCCC | 996 |
rs540011474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138597 | CTTTCTCTTCCTCTC[C/T]GAGTCCCTGACTAGA | 996 |
rs540082979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127788 | GCTCACTGCAACCTC[C/T]GCCTCCTGAGCTCAA | 996 |
rs540104533 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182717 | TAATATTTCCATTGT[A/G]TAAACATATCAAAAT | 996 |
rs540129859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CDC27 | GRCh38.p7 | 17:47188814 | GGCAAGAGAGCGCTT[G/T]GGGTGCATTTTCGGC | 996 |
rs540131733 | in-del | -/GA | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47179132 | CCGACTATAAATCTC[-/GA]GAGAAAGACAAATGG | 996 |
rs540147156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166301 | TTCATAATTTTAGGA[C/T]TATTCAGATTTCTAT | 996 |
rs540157797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174940 | CAGCCTGGGCAACAG[A/C]GAAACTCGGTCGAAA | 996 |
rs540160297 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120761 | GTTAGCAGCTAAATA[C/T]TGCACTGCCTTTCAT | 996 |
rs540171113 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141123 | CTAGAAGAGAGTCCA[A/G]GATATCATATGCACA | 996 |
rs540193399 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118972 | CACATAAATTCCTGC[C/T]ACAAAAAGATAATTA | 996 |
rs540250509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166861 | TGAATTATTTATTTA[C/T]TTAATTTTTTTGAGA | 996 |
rs540332169 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148627 | GAGCACATCATAATC[A/G]AATTGCTTAAAATCA | 996 |
rs540364625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47145727 | CCAACATGGTGGAAC[C/T]CCATCTCTACTAAAA | 996 |
rs540392408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47182999 | GCTGCTGGAGTGCAA[C/T]AGGAGCAAGACTCCC | 996 |
rs540467481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47135245 | CCCACTTACTGTTAT[C/T]AAAAGCATGCTCCTA | 996 |
rs540500513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164574 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCAG | 996 |
rs540504663 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118942 | AATCAGTACCAGAAA[C/G]ACTCTCACCTCTGGC | 996 |
rs540714165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47137474 | ACAAAAATGGAGGAG[C/G]TTCAGTAGATACTCA | 996 |
rs540754037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47188109 | TTTACTGTTTGATAC[A/C]TCAAGCCTTTTAAGG | 996 |
rs540779379 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191288 | GAAACAATCTACCAC[A/G]CTAGATATGAGATGA | 996 |
rs540883546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47148137 | CAGGAGGGGCGGAGG[A/G]TGCAGTGAGCCAGAT | 996 |
rs540883820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156486 | GGAGTCTTGGTCTGT[C/T]GCCCAGGATGGAGTG | 996 |
rs540922513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47171565 | AAACTATACAATCAC[C/T]TAAACACAAGGGAGC | 996 |
rs540946925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155991 | ATTTCCTCCATGTTT[G/T]GGAAAAAGGCACTTT | 996 |
rs540999640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176831 | TCTTGGATCAATAAA[G/T]GCCTCAAAATGATAC | 996 |
rs541069776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145982 | TCTGGGAAGGAAATT[G/T]AGTTCAATCATGTGG | 996 |
rs541100804 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149658 | AGACTTCTTTTTCTC[A/T]TTTAAAAAAATTTCA | 996 |
rs541106439 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183154 | ACTACTTTTGAGATA[C/T]CTCACACCTGATCAT | 996 |
rs541138624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47177472 | ATCCCAGCTACTCAG[A/G]AGGCTGATGCAGGAG | 996 |
rs541175937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47187254 | CCTGATGGGTACTAT[C/G]TAGAAACAGGCTACA | 996 |
rs541177016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168027 | GGGAAAGAGAGGTGC[A/G]GAGCTTCCATGGCCT | 996 |
rs541207930 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127703 | CTGTGCCTGGCCCTA[-/T]TTTTTTTTTTGTTTT | 996 |
rs541246408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135999 | CAAAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 996 |
rs541254523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160029 | TTCAAACAAACTAGA[A/G]GTGGTAGGTCTTTTT | 996 |
rs541273451 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173373 | TAGTGCTGCAGCTAC[-/A]AAAAAAAAAAAAAGA | 996 |
rs541307165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143137 | ACCATCCCAGCTAAT[C/T]TTTTTTTTCAGAGAT | 996 |
rs541310495 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134474 | CACCATGCCTAATTG[-/T]TTTTTTTTTTGTTTT | 996 |
rs541395812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47122942 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACCG | 996 |
rs541503593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127108 | CCTAAAAGAAGGTTT[G/T]TAAAGACTCCAGTTA | 996 |
rs541511442 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47168490 | TATAAACCTTTGAGG[G/T]TGGGGACTGTGAGTT | 996 |
rs541537679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174199 | CTCACAAGTAACTTG[A/G]CAGCAGAAAAAGATA | 996 |
rs541554712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47165343 | GCACTGCATCCTCTC[A/C]CCAGCACTTGGTATT | 996 |
rs541559172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47123715 | CCATGCCTGGCTAGG[A/G]TATCATTTTCTTAAG | 996 |
rs541610426 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47169134 | AGCTGGAACTACAGG[-/T]TATGTGCCACCACAC | 996 |
rs541676923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136430 | AACCCCAAAGATAAC[C/T]GTATCTGACAAAAAA | 996 |
rs541727544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47129053 | TGGGATTACAGGCGT[A/G]AGCCACTGCGCCTGG | 996 |
rs541793780 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138965 | GGGAAAGCCCTGGTC[A/G]TTATCTTCACAGGAT | 996 |
rs541800959 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118999 | ATTATACTTCAGCAA[A/G]TTATGTTCTAAGCTT | 996 |
rs541845177 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125133 | TAAAGTTGCCCAGGC[C/T]GGTCTTGAACTCCTG | 996 |
rs541853068 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CDC27 | GRCh38.p7 | 17:47154047 | TGAGTCATGGTCACA[C/T]CACTGCACTCCAGCC | 996 |
rs541877751 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47147456 | ACTAGGCATAGAAAA[C/T]AGCAGGAAAATATAA | 996 |
rs541891485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47163463 | CCCAGCACTTTGGGA[A/G]GCTGAGGTGCCAGGA | 996 |
rs541921777 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157533 | ATCAAATTTACCCCC[A/C]AAAAACCCATCTATC | 996 |
rs541966797 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119783 | AACCTATCTCCTTCA[C/T]AAGAATGTTTTTTCC | 996 |
rs541967922 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189274 | ACCAGCGACCGTTAC[C/G]GGGGGATGGGGGAGG | 996 |
rs541975802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47125647 | CTCCCAGGTTGAAGC[A/G]ATTCTCCTGCTTCAG | 996 |
rs541976195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47133586 | CTGGGATTACAGGCA[C/T]GCGCCACCACACCCA | 996 |
rs542032486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47169548 | TACTTGGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 996 |
rs542102158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132170 | CAACACAAAAAAGGA[C/G]CAATTTTTATCACAG | 996 |
rs542104291 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128528 | ACTAGAACTAGTCTC[C/T]GTGTTATAAGCTCTC | 996 |
rs542120720 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181089 | AACCCTATCTCTACC[-/A]AAAAAAAAAAAAAAA | 996 |
rs542125795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47126579 | ACTGATGAGATTAGA[A/G]CTTGGGTTTCTTGAA | 996 |
rs542228092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47135043 | TTATCATCCTTATTT[C/T]GAATAAGGAAACTGA | 996 |
rs542275306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47144119 | GAATTTGATCAGTTC[G/T]TTTCGTGGTTTCTCT | 996 |
rs542336690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47143201 | ACTCCTAAGCTCAAG[C/T]GATCGGCCCACCTTG | 996 |
rs542453399 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47176977 | TTGGGCTCTCAGTAT[-/C]CTGGTTAATAGAAAA | 996 |
rs542552056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47170276 | CAATCATAGTTCACA[C/T]GGCCTCAAATTCCTG | 996 |
rs542556996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158935 | TTTTTGTATTTTCGT[C/T]GAGATGGGGTTTTGC | 996 |
rs542619168 | in-del | -/T | 0.0015984 | 0.0282249 | intron-variant | CDC27 | GRCh38.p7 | 17:47136431 | CCCCAAAGATAACCG[-/T]TATCTGACAAAAAAA | 996 |
rs542622400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47135280 | TATAGACCTCAAAAT[C/T]ACAATTTCTAAAGGC | 996 |
rs542644205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159450 | AGCTTCTTGGGCACA[C/T]GTGCCAAGACGATGC | 996 |
rs542797985 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47183399 | TCTGCAATGAGTATA[A/T]TAATTATAATTTTAA | 996 |
rs542812793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175810 | AACAGAGCGAGACTC[C/T]GTCTCAAAAGAAAAA | 996 |
rs542850665 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128994 | CCCGGCTGGTCTTGA[A/T]CTCCTGACTCAGGTG | 996 |
rs542851414 | in-del | -/TTTAT | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47128336 | GCGCCCAGCCCTGAA[-/TTTAT]TTTAAAAGATTTTGC | 996 |
rs542885730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156582 | CCTCCTGAGTAGCTG[A/G]GATTACAGGCGCCCG | 996 |
rs542937414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47167826 | GTTAAGGGCTCAGTC[C/T]TCAAGACTGCCCTGC | 996 |
rs542939469 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155174 | TAACTCTCCAGAGTT[A/G]TAATCTCATGGTCAT | 996 |
rs542949853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47166953 | TCTGCCTCCCAGGTT[C/T]AAGCAATTCTCGTGC | 996 |
rs542951600 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47159122 | AAATATAGCATAAAT[G/T]ACCAGGTTTTTATTT | 996 |
rs543012046 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47134714 | CTCTTGACCTCATGA[C/T]TCGCCCATCTCAGCC | 996 |
rs543073752 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149453 | GTGGCAGAAGTTGCA[A/G]TGAGCCGAGATCGTG | 996 |
rs543091750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184072 | AGTGAAAGAAAATGG[G/T]GAGTAGAATGAAGAT | 996 |
rs543127346 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137837 | ATCTGGTCTTGTTCT[A/G]TTGTCCGGGCTGGAG | 996 |
rs543144307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179922 | ATAATAAACTAGAAA[C/T]TGCCTATTCTTTAAT | 996 |
rs543157898 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189090 | GGAGTGGCCCTACGC[G/T]GCTGCTTCCCGACCG | 996 |
rs543180471 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47186026 | CAAAGTATTAGCTTG[C/T]CCCAAATGTCAATAG | 996 |
rs543312822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47146996 | TGAGCCCAGGAGTTT[A/G]AGGCTGCACTGAGCT | 996 |
rs543333314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47187446 | GCTGGGATTACAGGC[A/G]CCCACCACCACGCCT | 996 |
rs543363274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148770 | AGTAAAGCAACATCC[C/T]TAAAAAAATTGTCAA | 996 |
rs543369680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47149246 | CCAGGTGCGGTGGGG[C/T]TCATGACTGTAATCC | 996 |
rs543376537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47153832 | TCATGTTTATAATCC[C/T]AGCACTTTGAGAGGC | 996 |
rs543408103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132450 | CAATTAGTAAAAGAA[A/C]AAGTATAGAATCTGG | 996 |
rs543423513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178501 | GATCACATGACTGCA[C/T]TCCAACCTGGGTGAC | 996 |
rs543481741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47125728 | TTTGTATTTTTAGTA[A/G]AGATGGGGTTTCACC | 996 |
rs543508305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179270 | AAATATAGAAACTGC[C/T]ACTAGTGACATAGGA | 996 |
rs543563765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160363 | CTCCCGAGTAGCTGG[A/G]ATTACAGGTGCACAC | 996 |
rs543610732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47185268 | ACTGCAAGCTCCACC[C/T]CCTGGGTTCACGCCA | 996 |
rs543620103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47130178 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 996 |
rs543654354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145258 | AGAGCTCAGTGGTCC[C/T]ACTGTGTTGAAAAGA | 996 |
rs543656224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47136543 | GTCAACAGTAAGTAT[A/G]GTGTTGAGGCAGAAA | 996 |
rs543691241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47177712 | ACACAAGGTTTTCAG[C/T]TGTTTCTCTTTCTTT | 996 |
rs543701831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138231 | TGGTTCAGTAGCACT[A/G]ATTCAGTGTTCATGT | 996 |
rs543730301 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129076 | GCGCCTGGCCCATAC[A/G]TTCATTTTCATCTGT | 996 |
rs543738144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47123071 | GATGAACTCATACCA[A/G]CTTTTGAGTTCCTTT | 996 |
rs543740908 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132441 | AATTTAGTTCAATTA[C/G]TAAAAGAACAAGTAT | 996 |
rs543751559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176943 | ATGTTGCCATTTGTA[C/G]GCATATATTTCTGTG | 996 |
rs543762585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47146042 | ATTTAAAAACCCTAA[C/T]AAAAATTTTGAACAC | 996 |
rs543832118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47165426 | TTCCTTAATGGCTAA[C/T]GATTTAGAACATCTT | 996 |
rs543840744 | snp | A/G | 1.75483e-05 | 0.00296207 | intron-variant | CDC27 | GRCh38.p7 | 17:47123863 | TGAAAGTCACTGTTT[A/G]GGACCATGACCCCAG | 996 |
rs543856189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47157972 | AGGACACCAGATACT[G/T]GAAAATAGATTGGTT | 996 |
rs543913090 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47154418 | GTTTATTTAACTATA[C/T]GCTGAAATAAACTAA | 996 |
rs543959368 | in-del | -/TTTAT | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47138412 | CAATGACAATACTAA[-/TTTAT]TTTAATTTAAAATTA | 996 |
rs543966823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134591 | AGTGGTTTTCCTGCC[C/T]CAGTCTCCCAAGCAG | 996 |
rs544015741 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163268 | AAAGAAAACCTAACA[C/T]ACCTTAGCTACAAAA | 996 |
rs544046852 | in-del | -/TTT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123420 | TTTTTTTTTTTTTTT[-/TTT]CTTTCTGAGACAGAA | 996 |
rs544171271 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47174227 | ATAACAGTACCCCAA[A/T]CACAACTAAAGAAGC | 996 |
rs544208833 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142434 | TAATTTTTTGCTATT[C/T]TCCTGTAAAAGGGAA | 996 |
rs544316520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155801 | ACAAAAACACTTAAA[A/C]AATTAGCCAGGTGTG | 996 |
rs544356957 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118240 | AGACTAAATACTGGT[C/T]ATCACTGAGTTTTTG | 996 |
rs544357932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127208 | TTTGAGGCTTCAGTG[A/G]GCTATGATTGCACCA | 996 |
rs544364019 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47181165 | GAGGCTGATGTGGGA[A/G]GATCGCTTGAGCCTG | 996 |
rs544389285 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191137 | AGGCCTGTGAGCATC[A/G]CTTCTTGTTGGTCAG | 996 |
rs544442341 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139764 | TGCTAGGAATCATAG[A/G]CCCTACCTATTAATT | 996 |
rs544518902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47126073 | TTACCTTAAAGACTT[A/C]AGATTTAAATAATTA | 996 |
rs544629949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147602 | AAGAGACTGGATGAG[A/G]TGGCTCATGCCTGTC | 996 |
rs544696178 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126062 | AGCTCTTACTTTTAC[C/G]TTAAAGACTTAAGAT | 996 |
rs544698743 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181214 | GAGCTGAGATGGTCC[C/T]ACTGTACTCCAACAT | 996 |
rs544719175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47144295 | AATGACTCGTTACTA[C/T]AAAATAGTAAAGATT | 996 |
rs544771109 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47126882 | CACAGCAACCTCCGC[C/G]TCATGGGTTCAAGCG | 996 |
rs544791770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47171742 | TTATTACCATAACAA[C/T]GAAATCTCCATAATA | 996 |
rs544887011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155206 | CTATTTTAGTAGTTC[C/T]CCGGCCTCAGGACCT | 996 |
rs544919030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164509 | TCAAAACTAGGAAAT[G/T]GACATTAGTACAAAA | 996 |
rs544965176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145375 | CAAAGATCTGCAGAG[A/G]GCTTCCCTAGAGTCT | 996 |
rs544993291 | snp | A/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191239 | AACACCACAAAGGGC[A/G]TGTGCCATGGGAGGA | 996 |
rs545028167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152222 | TTGTGACCATCCTCC[A/T]TTTATTACATACCTT | 996 |
rs545079899 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158441 | CTAAGTTACCAATTT[C/T]TCCCATCTGCTAATC | 996 |
rs545149417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47121855 | AGCAATTCTCCTGTC[G/T]CAGCCTCCCGAGTAG | 996 |
rs545253487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47168004 | AAGAGTGCATAGGGC[A/G]AGGCATGGGGAAAGA | 996 |
rs545315642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47149403 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 996 |
rs545384648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47129022 | GTGATCCGCCCGCCT[C/T]GGTCTCCCAAAGTGC | 996 |
rs545477759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176635 | TTAGGAACAGATCCT[C/T]ACAACAATTAGATAC | 996 |
rs545495064 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47129832 | TATGATGATAATCAA[C/T]AGTCTATCTTTAGAG | 996 |
rs545508313 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181352 | TGATTAAGTAAATCA[C/T]AGCATATAAACCTGA | 996 |
rs545511581 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47167028 | CCCGGCTAACTTTTT[A/T]ATTTTTAGTAGAGAC | 996 |
rs545591095 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121800 | GTTGGAGTGCAATGG[C/T]GTGATTTCGGCTCAC | 996 |
rs545627679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152387 | AAAGGAGTTCAGAGG[A/G]GTAGATTTTAAAAAA | 996 |
rs545731480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47188398 | CAAAGCATACCCTGG[G/T]GTAAAGGCAGTGAAA | 996 |
rs545812411 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146063 | TTTTGAACACCAAAA[C/T]TTGGCTCAAATTCCT | 996 |
rs545824203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47161374 | GAAATGAAGAAAGGG[C/T]ATACAAAAAAACATT | 996 |
rs545862443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47133466 | TTTTTTGAGACGGAG[A/T]TTCGCTCTTGTTGCC | 996 |
rs545881486 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139011 | TATTATGGTTTTTAT[A/G]TGAATGAGTATTAAC | 996 |
rs545900282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47178415 | TAGCATGTGCCTGTA[A/G]TCTCATCTAGTAGGG | 996 |
rs545908863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47170200 | TCCCTCCCTCTCTCT[A/G]TCTTCCTTTCTTTAA | 996 |
rs545910047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47153056 | AACTTCATAAGCCTT[C/G]CTCCGCCTTTTCCAA | 996 |
rs545956731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47139114 | TTTATATACAAGCCA[C/T]GGTAAGAACATGAAC | 996 |
rs545968424 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174012 | GGCAGGAGAATCGCC[C/T]GGACCCAGGAGGCAG | 996 |
rs546042034 | snp | A/C | 1.71923e-05 | 0.00293187 | intron-variant | CDC27 | GRCh38.p7 | 17:47123876 | TTGGGACCATGACCC[A/C]AGTCTTTACCTTTCC | 996 |
rs546218758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148939 | CAAAAATTAGCTGAG[C/G]ATGATAGCACATGCC | 996 |
rs546281759 | in-del | -/GA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175046 | GAGAGAGAGAGGAAG[-/GA]AGGAAGGAAGGAAGG | 996 |
rs546373045 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146728 | TCTCAGAATAAAACT[G/T]TAAAATACCTAAAGG | 996 |
rs546395575 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141952 | GCTCAAAATATTTAT[A/G]GCTTCTTTGCAGTTG | 996 |
rs546405897 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170153 | ACACAAATTTTTTCT[C/G]TCTCTCTCTTTCCTT | 996 |
rs546477703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178683 | TGTATTTAGTCCTTA[A/C]AACTATCTTGTTAAA | 996 |
rs546484439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148369 | ATAGCAATAAACACT[A/G]TCCAAAATGAAACAC | 996 |
rs546498400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156300 | CGTGCCACCACACCC[A/G]GCTAGTTTTTTGTAT | 996 |
rs546596940 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47133690 | TGATCCGCCCGCCTC[G/T]GCCTCGGCCTCCCAA | 996 |
rs546672522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127292 | AGCTTTTTAAAAGGA[C/T]AAAACCAGTAAAAAT | 996 |
rs546765103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47173775 | AAATGGGAATACGGA[C/T]TGGTGATTTAGGCAA | 996 |
rs546787496 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130218 | TACAAAAAATTAGCC[A/G]GGCGTGGTGTCACAC | 996 |
rs546932985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140560 | AAATGGGAAAAAAAC[A/T]CAGAAATTAAGTTGA | 996 |
rs546944507 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47134130 | TTTCAAACTCTTAGC[C/G]TCAAACAATCCTCCC | 996 |
rs546975079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47180516 | TTCCTGCCCCTGAGG[C/T]TTAGGCCTTGTTCTC | 996 |
rs546978917 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190390 | GCTCCCCTTCTCCCC[A/C]CAAAAAGAGTGAACC | 996 |
rs547047478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47131063 | GGACTGAGACCCTAA[A/C]TACTAGTTCCCGAAA | 996 |
rs547202708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147330 | CGTGAACCCGGGAGG[C/G]GGAGCTTGCAGTGAG | 996 |
rs547219810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168303 | GCTGCCAGTCCCCAT[C/T]CTGAAGCTACCTAGG | 996 |
rs547238999 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47169374 | CATGGGGCCGGGTAC[A/G]GTGGCTCACACCTGT | 996 |
rs547244539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155331 | GCTCACTGCAACCTC[C/T]ACCTGCTGGGTTCAA | 996 |
rs547267464 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136212 | CATAGCTATCGGAAG[A/T]GACAGCAGCATTGGC | 996 |
rs547375572 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47130315 | CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA | 996 |
rs547394977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136166 | ACAAACAAACAAAAA[A/G]AAAACTGAGTTCTTA | 996 |
rs547401828 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167588 | AATTTTATGACAGAA[C/T]GTTTAATGTGATAAT | 996 |
rs547510445 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47140551 | AAAAAGAAAAATGGG[-/A]AAAAAAACTCAGAAA | 996 |
rs547568828 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127410 | TAGCCTATTTTTACG[-/T]TTTTTTTTTGAGATG | 996 |
rs547627730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47136820 | CCCAAGCACTTTTCA[C/T]CCCAATCACCATTTC | 996 |
rs547646238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47151533 | TGTACCTAAACTATA[A/G]AAAGGGTCATGTGCA | 996 |
rs547670967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176001 | CCCTCATTTTTTTTT[A/C]ATCCGGTAAGGACTA | 996 |
rs547708420 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156676 | TGTTCTTGAACTCCT[C/G]ACCTCAGGTGATCTG | 996 |
rs547734075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175274 | AGCTTTTAAACCAGA[C/T]AGACGCCTCTTCTTC | 996 |
rs547759728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166560 | CAGCTTTGGTTTCTA[C/T]GATTTTCTCTATTGT | 996 |
rs547851277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47164010 | CTCAGGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 996 |
rs547856123 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47121974 | ATCTCCTGACCTCAG[G/T]TGATCCACCCACCTC | 996 |
rs547878291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47159044 | GGCGTGATCCACCAC[A/G]CTTGGCCTTAATTTT | 996 |
rs547909287 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47150771 | GGCACGGTGGCTCAT[G/T]CCTGTAATCCCAGCA | 996 |
rs547938493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179464 | GGAAAGCGGAATCAG[A/G]CAGATTACTAGTTAC | 996 |
rs547976492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135437 | TGATGATGATGATGA[C/T]GATGATGATGATGGG | 996 |
rs547979395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128608 | TGATTATTTGGTTAA[C/T]GTCTGTTTTCCTAGA | 996 |
rs547990423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47155392 | CTGGGATTACACGTA[C/T]GTGTCACCATGCCGG | 996 |
rs548015932 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153999 | GAGGCTAAGGTGGAA[A/G]GATCACTTGAGCCTG | 996 |
rs548018199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128120 | ACTGCAACCTCTGCC[C/T]CCTGGGTTCAAGTGA | 996 |
rs548047355 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118915 | ACGATCCTTTTATCC[C/T]TGGTCTCAAAAAATC | 996 |
rs548135764 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47162228 | AATTCATGTACTTTC[-/A]TTTTATTTCTGGCTT | 996 |
rs548249638 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118286 | CAGCATGGTTCAAAT[A/G]TTACTTGTAGTTCTC | 996 |
rs548328207 | snp | A/C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171791 | ACAGTGTAAACATTT[A/C/T]GAATGTTACTGAAAT | 996 |
rs548350958 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47139341 | GCGCAATCTCGGCTC[A/C]CTGCAAGCTCCGCCT | 996 |
rs548373094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47125833 | AGGCGTGAGCTGCTG[C/T]GCCTGGCCTTTAAAG | 996 |
rs548451089 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47162983 | CCTCTAATTATTCAA[C/T]AGAGAGATAAAAGGG | 996 |
rs548468206 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47145827 | ACTTGAACCCGGGAG[A/G]TGGAGGTTGCAGTGA | 996 |
rs548482881 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117208 | AACAAAGTTTGCACT[C/T]ACAAAGAAAAATAAA | 996 |
rs548521942 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140312 | AGAGACAGGGTCTCA[C/T]CACATTGGCCAGGTT | 996 |
rs548535562 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130746 | GCCAGGCGTGGTGTC[A/G]GGCACCTGTAATCCC | 996 |
rs548608109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47161412 | AGTAATAGGGTGGAA[C/T]GTGGCAAATCAGTGC | 996 |
rs548608433 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133446 | CAAGCTGTTTTTTTG[-/T]TTTTTTTTTTGAGAC | 996 |
rs548628390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136041 | CAGCTACTCGGGAGG[C/T]TGAGGCAGGAGAATG | 996 |
rs548655452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132067 | GCAATGAAGTGACTT[G/T]TGCAAGGGATAAGGG | 996 |
rs548695905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135545 | TGTTATAGATGAAGA[A/C]AAGGTATTAAACACT | 996 |
rs548733552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160505 | TGTTGGGATTACAGG[C/T]GTGAGCCACAGCACC | 996 |
rs548794226 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47128643 | ACTAGATAGTAGGCC[A/C]CTCAAAAGCAGGAAA | 996 |
rs548848967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47183804 | GCAGGTGCTTATATG[C/T]TGAATGAATAAGCAA | 996 |
rs548934011 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119309 | TCTGTTAAATATCTC[G/T]CTGGCACCTGATACC | 996 |
rs548996544 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124592 | CCCGGCCCAGTGATT[C/T]ATTTTTTAACGAAAA | 996 |
rs549257779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47149637 | TTATGTGTGTAAATA[A/T]AAAATAGACTTCTTT | 996 |
rs549268414 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126148 | TTAGAGATGTTGAAA[C/T]GGCCCCCTTGATTTT | 996 |
rs549270533 | snp | C/T | 1.71968e-05 | 0.00293225 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158209 | CCACCCACCTACCTA[C/T]TTCACATAATGATTC | 996 |
rs549356748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174002 | CGGAGGCTGAGGCAG[C/G]AGAATCGCCTGGACC | 996 |
rs549396523 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47161413 | GTAATAGGGTGGAAC[A/G]TGGCAAATCAGTGCT | 996 |
rs549402643 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | CDC27 | GRCh38.p7 | 17:47134357 | TCGCCCGGGCTGGAG[G/T]GCAATGGCGTGATCA | 996 |
rs549418616 | snp | A/G | 7.25281e-05 | 0.00602153 | intron-variant | CDC27 | GRCh38.p7 | 17:47181559 | AATGAATAGATTTCA[A/G]ACCTTCTGCATAAAG | 996 |
rs549445799 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145521 | GATGTCTTTGTTATT[C/T]ATTATGAGCTCCTGG | 996 |
rs549477650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178897 | AACCTCCGCCTCCCG[A/G]GTTCAAGCAATTCTC | 996 |
rs549503249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47164895 | TTTTACACGTTTATA[C/T]AGAGAATATTATCAC | 996 |
rs549514301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47131881 | TCGCTATGTTGCCCA[A/G]GCTGGTCTCCAACTC | 996 |
rs549553383 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160900 | ATATGACAAAGAAAG[C/T]ACTACCAGTTGAAGG | 996 |
rs549631476 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47148210 | TCTCAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 996 |
rs549632866 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47139023 | ATGTGAATGAGTATT[-/A]AACACAAGGACAAAT | 996 |
rs549633420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140616 | TTTGGGTCACCACTA[C/T]AACTAGGGGAAACAA | 996 |
rs549678992 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47133795 | TTTTTGTCACCCAGG[G/T]TGGAGTGCAGTGGTG | 996 |
rs549719473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141270 | TTTAAGTTGGGGGTG[G/T]AGAAAATGCTTTGGG | 996 |
rs549831950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47130388 | AAAAATAAAAAAAGA[A/G]AAAAAAAAGAAAAAT | 996 |
rs549891986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47161579 | AACACGGTGAAAACT[C/T]GTCTCTACTAAAAAC | 996 |
rs549904234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160639 | AGTTCAAATGCTTCA[A/G]TATCAAATGGAAAAA | 996 |
rs549906691 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47169671 | AAAAAAAATAGAAAC[A/C]AACAAAAAAACCTAA | 996 |
rs549939967 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150711 | GAGATAAAATGGAAT[C/T]AACAATACAAAGAAC | 996 |
rs550037000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136976 | GTTAATTTAAGAGTT[C/T]GTTAAAGACGTACAT | 996 |
rs550037832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47131270 | AAAATAATTTTAAGT[A/G]GACACATTATCTCTC | 996 |
rs550089117 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47186761 | ATTAAAACTTTAAAG[A/G]AAAAAAAATGCAGAA | 996 |
rs550105003 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166119 | TTTTTGTGTATACAT[A/G]TATTCTTAAGGAATA | 996 |
rs550105167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47148626 | AGAGCACATCATAAT[C/T]GAATTGCTTAAAATC | 996 |
rs550121554 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47159582 | AGCCTCTGCGCACGG[C/G]GACAATCGAGAGTTT | 996 |
rs550123963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47137560 | TTTGTAAAACCAAAA[G/T]CAATACTTGCAGTGC | 996 |
rs550261915 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119702 | ATTTTATATGCATAA[C/T]TGAATTCTTAAAATT | 996 |
rs550297231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47144593 | TATTCTCTTTAGAGC[A/G]AAAGGAGCCTCTGTA | 996 |
rs550313556 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156286 | TGGATCTACAGGCGC[A/G]TGCCACCACACCCGG | 996 |
rs550320079 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124981 | GGAGTGCAGTGGTGC[A/G]ATCTCTGCTCACTGC | 996 |
rs550329683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172416 | ATATTTTTCTAATAA[A/G]TCTTTCGGGAGGATA | 996 |
rs550397651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47121105 | AGAAAAATTGTATTA[C/T]ATTCAGAGAGATAAA | 996 |
rs550462707 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47164039 | AAAATGCTGGGATTA[C/T]AGGTGTGAGCCACCC | 996 |
rs550475180 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146901 | AAGACCCCATCTCTG[C/T]AAAACTAAAAAAAAA | 996 |
rs550504197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47126616 | AAACGCTGATTTATG[C/T]GGCCTATCTGGTAGG | 996 |
rs550636646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47170957 | AATAAGAAAATTAGC[C/T]AGGTGTAGTGACACG | 996 |
rs550648394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141273 | AAGTTGGGGGTGGAG[A/C]AAATGCTTTGGGAAG | 996 |
rs550648804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47133644 | GGGTTTCTCCATGTT[A/G]GTCAGGCTGGTCTCG | 996 |
rs550684970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140431 | GTTTTTCATTCAGGC[A/G]TGGTAACAAGATAAA | 996 |
rs550924144 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47187522 | GGCCAGGCAGGTCTC[C/G]AACTCCTGACCTCAG | 996 |
rs551002464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136071 | GGCGTGAACCTGGGA[A/G]GCGGAGCATACAGTG | 996 |
rs551005940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47154396 | TAAAAAGTAAAAATA[C/T]GATTATGTTTATTTA | 996 |
rs551040262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47125897 | CTCCTTCACTGCTAC[A/C]ACACACACAATTCAG | 996 |
rs551136144 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CDC27 | GRCh38.p7 | 17:47189324 | TTCCGAGCGGGACAC[A/G]GGAATACCCGAAGTG | 996 |
rs551224177 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47162458 | TGGAGAATTAGTCTT[C/T]GCCATTTTTATACTA | 996 |
rs551270080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47146693 | AAGGGATCAAGCTGT[C/T]TCCAAGCAACTTTAC | 996 |
rs551281316 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120901 | ACGTCAGCACTAGTC[A/G]CACATCCAGTTGTAA | 996 |
rs551315211 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176950 | CATTTGTACGCATAT[A/T]TTTCTGTGAGTTTGG | 996 |
rs551316770 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47149756 | GGTCAGGAGTTTGAC[A/G]CTAGCCTGGCCAACA | 996 |
rs551402780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47142803 | CCTGCTTCAGCCTCC[C/T]GCGTAACTGAGATTA | 996 |
rs551527416 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183284 | GATCACTAGCTAACA[A/T]TGTACCAGTACATCT | 996 |
rs551538634 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47185441 | GCCTGCCTCAGCCCC[C/G]CAAAGTGCTGGGATT | 996 |
rs551571928 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190517 | ATGATATATTCCATT[A/G]CTTGGAAATTTCCCT | 996 |
rs551667808 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47150538 | GAGGCAAGGAAAAAT[A/C]CTCCTCTAAAGATTT | 996 |
rs551713292 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120874 | GACTCAGTATACAGA[A/G]GGACAAGAAACACGT | 996 |
rs551715469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175158 | TTGGCTTCAAAATTG[G/T]AAAGGTCTTTTGAGT | 996 |
rs551763186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174595 | TATTGAGAAATCAAT[C/T]GTGTACTAGTTAAAT | 996 |
rs551826058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47182499 | ATTTTCTTGACCTTT[C/T]TCTTGGTTTTCTTCA | 996 |
rs551849059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128446 | TATCTTCTTTTTTCA[A/G]TACTTGTTTCAGGCT | 996 |
rs551898740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158410 | AAGTTCAGAGAGCAC[G/T]CTTTGTGATGCTTCT | 996 |
rs551905053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166474 | TCTTTCATTCCTGAT[A/G]TAAGTAATGGTGTTC | 996 |
rs551914724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47187534 | CTCGAACTCCTGACC[G/T]CAGGTGATCCACCCG | 996 |
rs551971981 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120433 | ATTCCTTGGCAATCA[A/G]GTCACTGTTATAGGC | 996 |
rs551974723 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139985 | AGGTCTAGGTAATAA[A/G]AAAAAAAAGAAAGGA | 996 |
rs551977854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47186882 | TACTCTCATTGCTTT[C/T]CAAATACACGCAATC | 996 |
rs551978471 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47134851 | GCTGGTCTCAAACTC[C/G]TGGTCTCAAGTAATC | 996 |
rs552028486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47183562 | TGTCTAATTTTACCA[C/T]TCCTATCTAGATACA | 996 |
rs552168679 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47161712 | TCGAGATCATGCCAT[C/T]GCACTCCAGCCTGGG | 996 |
rs552187448 | in-del | -/AAC | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47164819 | CAAGATTCCATTTCA[-/AAC]AACAACAACAACAAC | 996 |
rs552343101 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47146234 | CACTTTCCTGGACTC[G/T]GTGAGGTGCTCTAGC | 996 |
rs552380474 | in-del | -/A | 0.222928 | 0.24853 | intron-variant | CDC27 | GRCh38.p7 | 17:47135780 | AGACAATACACATTT[-/A]AAAAAAAAAACAACA | 996 |
rs552409466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47131515 | ACTTGCTAGGGGGAA[A/G]AAAAGAGAGAAGCTG | 996 |
rs552456274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159632 | CTGCAGATGGCAGTG[A/G]CCACCTCCTTGGAGC | 996 |
rs552481540 | in-del | -/AAT | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47144786 | CAAAGAATTTCAGAA[-/AAT]AAAAAGATATATATT | 996 |
rs552483787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124904 | GACCACTCTGAGAAT[C/T]ATTACTTTAAAGACA | 996 |
rs552609236 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167135 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 996 |
rs552656513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47145678 | CAGGCCAAGGCAGGC[A/G]GATCACGAGGTCAAG | 996 |
rs552740004 | in-del | -/AAAAAAAAAAAAAAAAAAAA | 0.480539 | 0.0967035 | intron-variant | CDC27 | GRCh38.p7 | 17:47181255 | GTGAGACCCTGTTTC[-/AAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAACCC | 996 |
rs552783866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47123143 | CTTTCAGGTAGTAAG[C/T]TTCCAATAAATATCA | 996 |
rs552809855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47173509 | TGGTTTCTTTTCACC[C/T]TATAAGTTTTTAAAA | 996 |
rs552854950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147981 | CAAGGTGGGCGGATC[A/T]CGAGTCAGGAGTTTG | 996 |
rs552979168 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156594 | CTGGGATTACAGGCG[A/C]CCGCCACCATGCCCA | 996 |
rs553015260 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47140114 | TTAATTCCAAGAAGT[-/G]GTCATATGATATATA | 996 |
rs553064432 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117504 | CAAATTAGAGTAAAA[C/T]TTAGTTTCTACATCT | 996 |
rs553245930 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47125593 | GGAGTTTTGCTCTGT[C/T]GTCCAGCCTGAAATG | 996 |
rs553245963 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47133190 | GTTGCCCAGGCTGGA[A/G]TGCAATGGTGCAATC | 996 |
rs553358140 | snp | A/G | 2.15552e-05 | 0.00328286 | intron-variant | CDC27 | GRCh38.p7 | 17:47122652 | TTGTGAGCTTCAACT[A/G]TAAAATTCTAACTAT | 996 |
rs553513528 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147428 | AAACAAACAAACAAA[A/C]AAAAAAAAAAACACT | 996 |
rs553568103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132511 | TCTTAGAGGAGAGGC[A/C]AAAAATACCAGTTAT | 996 |
rs553644820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47121645 | ACAGGGTCTCACTGG[C/T]TAGTCGTGAAATCCT | 996 |
rs553673808 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47127102 | CCTGGCCCTAAAAGA[A/C]GGTTTTTAAAGACTC | 996 |
rs553679540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128982 | TTCACCATGTGGCCC[A/G]GCTGGTCTTGAACTC | 996 |
rs553686289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47167738 | CTAAACACACCAAGC[A/G]TCAAACGCCAGCTGA | 996 |
rs553732108 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158761 | ACAGCTGAGACTATA[A/G]GTGCGCACCACCATA | 996 |
rs553739887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47179149 | GAGAAAGACAAATGG[A/G]CGACAAAGAACTAGT | 996 |
rs553775237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47129587 | AAGGTGAGAACCAAC[A/G]TGACTCAAAACCAAC | 996 |
rs553788535 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161801 | ATTGTTTGAGGATTA[C/T]CCTAAGCTTCAAATA | 996 |
rs553880711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159339 | TAGTTGTAGGTCTTA[C/G]AGATGGCATCAAAGG | 996 |
rs553894446 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146173 | TCTAATCCTATGGAT[C/G]TCCTAATTATGTCAT | 996 |
rs553984532 | snp | C/T | 0.000113598 | 0.00753564 | intron-variant | CDC27 | GRCh38.p7 | 17:47142199 | GTACATAATAAAATA[C/T]AAAGATAATATTAAG | 996 |
rs554003620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184005 | TACCACCAAATTACT[C/T]CTTTATGAAATCTGG | 996 |
rs554035726 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47165111 | CTTTTTTCACTTGCC[A/G]TAATAACCTTGTAAT | 996 |
rs554142134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175743 | ATCGCTTGAACCTGG[A/G]AGGCAGAGGTTGCAG | 996 |
rs554179106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47149270 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCAG | 996 |
rs554235842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47142828 | AGATTACAGGCATGA[A/G]CCACCACGCCCGGTT | 996 |
rs554304998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47174749 | TCACCTGAGGTCAAG[A/G]GTTCAAGGCCAGCCT | 996 |
rs554314879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47151522 | TGAAACCTATCTGTA[C/T]CTAAACTATAGAAAG | 996 |
rs554376776 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125193 | CCAAAGTGCTAGGAT[A/T]ACAGTTGTGAGCCAC | 996 |
rs554377282 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120440 | GGCAATCAAGTCACT[A/G]TTATAGGCAACGTCT | 996 |
rs554411835 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119619 | TAAAAATTTCAATAC[A/C]TTACAGTAAAGGAGA | 996 |
rs554451891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47149342 | ATGGTGAAACCCCGT[C/T]TCTACTAAAAATACA | 996 |
rs554493288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166021 | TTACTGGCTCAAATA[A/G]TAATTCTAGTTTCAA | 996 |
rs554496904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47177515 | CTGGGAGGCAGTCAG[C/T]CGAGATTGGGCCACT | 996 |
rs554522327 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122055 | ATGGCTTATAATTTT[A/G]ATTAAAGCCTTTCAC | 996 |
rs554554871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156533 | GCTCACTACAACCTC[C/T]GCCTCCCGGGTTCAA | 996 |
rs554574916 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47148589 | AATAAATCCAAAGGC[C/T]GAGAAACAACAAAGC | 996 |
rs554582023 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176564 | CAGAAAATGGCAATA[C/T]ATGAGGAGAAAAAAG | 996 |
rs554679449 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47188275 | TGGTCCATTACCAAG[G/T]CACAAAAGATACAGT | 996 |
rs554679591 | in-del | -/TTTA | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47151445 | ATTCATTATTTGAAG[-/TTTA]TTTGTCTGTTATTTT | 996 |
rs554700021 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47137897 | CCTCCGCCACCTAGG[C/T]TCAAGTGATCCTCCT | 996 |
rs554709674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160973 | AATGGACAAAGTAGG[A/G]AGCAGAAGTAGGATG | 996 |
rs554715027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147347 | GAGCTTGCAGTGAGT[C/T]GAGATCGCGCCACTG | 996 |
rs554852697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145107 | AGAGTAAAATGGAAT[A/C]AATTTATTCTCCCAT | 996 |
rs554895856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152922 | CTCTTTCTTTCCCTA[C/G]GAGAGCCTGGTCATT | 996 |
rs554897557 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174204 | AAGTAACTTGGCAGC[A/T]GAAAAAGATAACAGT | 996 |
rs555021515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166141 | TAAGGAATAGTGGCC[C/T]ATAGTTTTCCTTTTT | 996 |
rs555071811 | in-del | -/CTA | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47125321 | CGTGATCTTGGCTCG[-/CTA]CTACAACCTCTCCCT | 996 |
rs555080537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47127591 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCAAGT | 996 |
rs555255402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141366 | CCTTTTCTGGTATAG[A/G]CAGATAACTTAAGCA | 996 |
rs555268673 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127680 | GGCTGGGATTACATA[C/T]GTGAGCCACTGTGCC | 996 |
rs555297362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47182861 | CATCTCCTGGGGTAT[A/G]TATTTAAGAATCTCT | 996 |
rs555323260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47134506 | TTTTGTTTTGTTTTG[C/T]TTTTGAGATGGAGTC | 996 |
rs555356594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135063 | AAGGAAACTGAAACT[C/T]AGAGAAGTTAAATAA | 996 |
rs555404652 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191089 | TTGACAACAAAGTGC[A/G]CAAAAATAGAAGCTG | 996 |
rs555427720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47148058 | CAAAAATTAGCAGGG[C/T]GCAGTGGCACATGCC | 996 |
rs555462910 | snp | C/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141954 | TCAAAATATTTATAG[C/T]TTCTTTGCAGTTGTA | 996 |
rs555464689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128188 | GGTGCACACCACCAT[A/G]CCTGGCTAATTTTTG | 996 |
rs555492278 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120475 | TTGTTCCATCTGGCA[C/T]TTGCAAACACCATTC | 996 |
rs555539960 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147291 | GTAGTCCCAGCTACA[C/T]GGGAGGCTGAGGCAG | 996 |
rs555593124 | in-del | -/AA | | | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117783 | AAATATAAATATATT[-/AA]GAGTGTAAGTTTTAA | 996 |
rs555752592 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120658 | CATGATACTTTCCAA[A/C]AAAGGGAGATTAAAG | 996 |
rs555759396 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121470 | CAATCATCTATCTTG[C/T]TCTGTCACCTAGGCT | 996 |
rs555809315 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47154636 | TAAACAAGTTGCTTT[A/C]ATCAATTCCCAAACT | 996 |
rs555816659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47156328 | TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCATGT | 996 |
rs555830203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145279 | GTTGAAAAGAAAATG[C/T]TGAGAATTTGAGAAA | 996 |
rs556003301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47163518 | CCAGCCTGGGCAACA[C/T]AGGGAGACCCCATAT | 996 |
rs556015402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47126876 | TGGGCTCACAGCAAC[C/T]TCCGCCTCATGGGTT | 996 |
rs556075525 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47172766 | CTTATTTAGTCTATG[C/T]CTCTACTAAACTGAT | 996 |
rs556088508 | snp | C/T | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191088 | GTTGACAACAAAGTG[C/T]GCAAAAATAGAAGCT | 996 |
rs556148824 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47127877 | TGGCTAATTTTTGTA[-/T]TTTTTTTTGGTAGAG | 996 |
rs556159564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159763 | AATCTTCAAAACCTT[G/T]TGCTTGAGAGAGGCC | 996 |
rs556341295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184983 | CGCTCCTCTCCCTCT[C/T]CCCTAAAAAATGTTT | 996 |
rs556351764 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123683 | TCCCAAAGTGCTGGG[A/T]TTACAGGCGTGAGGC | 996 |
rs556376188 | snp | C/G/T | 1.73501e-05 | 0.00294529 | intron-variant | CDC27 | GRCh38.p7 | 17:47143872 | GTGACATACAGAAAT[C/G/T]TTTAAATTACCTTGG | 996 |
rs556399147 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146825 | ATCCCAACAACTCGG[A/G]TGGGTGAGGTGGGAG | 996 |
rs556445365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47157855 | GTACTGTTCAGGTCT[G/T]GTAAGTTTCAGGCAT | 996 |
rs556447851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47122755 | CTTGGCTCACTGCAA[C/T]CTCCACCTCCCAGGT | 996 |
rs556477578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168375 | ATCACTTTGGAGTTT[C/T]TAAGTGTATACGAGG | 996 |
rs556527885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189109 | GCTTCCCGACCGAGG[C/T]TGCCAGCCAAGCCCC | 996 |
rs556540954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47167841 | TTCAAGACTGCCCTG[A/C]CCCACCTTCAGAAAC | 996 |
rs556663756 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189949 | GAGAGGGCAATTGTG[A/G]TAAGATAAGGAAAGT | 996 |
rs556706760 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47163071 | TATTAAAATTGAGTG[A/T]TACACACAAAACCCA | 996 |
rs556707952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143677 | AACTTGAGAAAAAAA[A/G]TTTTTTAATTAAAAA | 996 |
rs556805675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47150046 | ATGCACTGTGGGGTT[G/T]ATAACATATATAGAA | 996 |
rs556836463 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149812 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGCACAT | 996 |
rs556842651 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118311 | GTTCTCGGAAAAATT[A/G]AAAATTTTAAGTGAT | 996 |
rs556915142 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173772 | TTCAAATGGGAATAC[A/G]GATTGGTGATTTAGG | 996 |
rs556944292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147882 | CTCCAGCCTGGGTGA[C/T]AGTGAGACCCTGTCT | 996 |
rs556965746 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | CDC27 | GRCh38.p7 | 17:47147427 | CAAACAAACAAACAA[A/C]CAAAAAAAAAAACAC | 996 |
rs556967567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47122174 | AGCAGATAAAACAGT[A/G]CTGGTTACATATTCA | 996 |
rs557024041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47139927 | TAAAATCAGTTTCCT[A/G]GTTTATCAATTTACC | 996 |
rs557046992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47179957 | AACAAAAACAAAAAG[A/G]AAATACTAGAAATAG | 996 |
rs557047562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47125436 | ATTTTTAGTAGACAC[A/G]CGGTTTCACCATATT | 996 |
rs557070711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47170151 | AGACACAAATTTTTT[C/T]TCTCTCTCTCTTTCC | 996 |
rs557086462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47153909 | GCAACACAGTGAGAT[C/T]CTGTCTCTACAAAAA | 996 |
rs557092318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47187941 | CTTACAGACAGGTAA[A/G]TTTCATAAGATATAA | 996 |
rs557107780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140729 | CCTGTCTGTGTATAT[A/G]CTACATACCAGTAAA | 996 |
rs557128253 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47133427 | ACAGGTGTGAGTCAT[A/G]GTGCCAAGCTGTTTT | 996 |
rs557168349 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117395 | GCTCACCCCACCTTC[A/C]CATGTTTTTCCCTGT | 996 |
rs557225754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147039 | CTGTACTCTAGCCTG[A/G]GCATCAGAGTAAAAG | 996 |
rs557246304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138001 | AGAAGGGTTTTGCCA[C/T]GTTGCCGAGGCTGGT | 996 |
rs557337386 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47124454 | ACACCCAGCTAATTT[C/T]TGTATTTTTAGTAGA | 996 |
rs557337552 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CDC27 | GRCh38.p7 | 17:47178557 | AATAAAAATAAGAAA[A/G]AAAAAAAAAAACCCT | 996 |
rs557376608 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178879 | GTAATCTCGGCTCAC[C/T]GCAACCTCCGCCTCC | 996 |
rs557377432 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185150 | AAACCTCTATAAGTT[G/T]TACTTAGACTTAAAT | 996 |
rs557410462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158768 | AGACTATAGGTGCGC[A/G]CCACCATATCCGGCT | 996 |
rs557423332 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131067 | TGAGACCCTAAATAC[C/T]AGTTCCCGAAAAGAG | 996 |
rs557476272 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120706 | TTCCCCACCCTACCC[A/C]CCATAAATTGTCATT | 996 |
rs557490976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174910 | GCAGTGAGCCGAGAT[C/T]ATGCCACTGCACTCC | 996 |
rs557587790 | in-del | -/T | 0.0551013 | 0.156571 | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117485 | CCAAAAAAAAAAAAA[-/T]TTTCAAATTAGAGTA | 996 |
rs557626874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135600 | ACAAAAGAAAGGCTA[C/T]CTATTTTGTACTTAG | 996 |
rs557662579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47187125 | AAACTTTCTACCACT[A/G]TCTCAAAAATCTAAT | 996 |
rs557663651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47135195 | ATATTATTATAATTA[C/T]AGCATACATAGTGTC | 996 |
rs557960814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47142164 | ACTGTAATGAACATA[A/G]AGAAATTTACTTAAA | 996 |
rs557996086 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191156 | CTTGTTGGTCAGAGT[A/G]AGACTCAGAGCCACC | 996 |
rs558083460 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47180749 | GCTGTGCTAAGGGCT[G/T]TAAATAAACCATCTC | 996 |
rs558152036 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47156387 | TCGTGATCTGCCCAC[C/T]TTGGTCTCCCAAAGT | 996 |
rs558157333 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141414 | CCAAAGAGTAAAAAG[A/C]CTTGTATTAAAGACA | 996 |
rs558200050 | in-del | -/AAG | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47127098 | GGCACCTGGCCCTAA[-/AAG]AAGGTTTTTAAAGAC | 996 |
rs558288731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47157553 | ACCCATCTATCAATA[G/T]ATCATAAAAGTTTAC | 996 |
rs558302893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127411 | TAGCCTATTTTTACG[G/T]TTTTTTTTGAGATGG | 996 |
rs558374744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47174334 | AGTAACTCCAACTTA[C/T]GGATAATGGCTGTCT | 996 |
rs558454041 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47168580 | AAGTGTGTTTAGCTA[C/T]AATGGAAATGAATCT | 996 |
rs558469727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47164959 | GGATATAAAACTGTT[C/T]TAATATCCCAAAGAA | 996 |
rs558486668 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47182779 | TGGACATTTGGGTTA[C/T]TTCTAGGGTGTTTTT | 996 |
rs558494726 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47135783 | CAATACACATTTAAA[-/G]AAAAAAACAACACAA | 996 |
rs558525492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47185048 | AGGTGCACTAATTTA[A/G]AAGATAAATAAACCA | 996 |
rs558614703 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47138076 | GAAGTGCTGGGATTA[A/T]AGGTGTGAGCCACCA | 996 |
rs558627086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145959 | CCAGCAACACCAGCC[A/T]GAGCTCCTCTGGGAA | 996 |
rs558627465 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47169178 | TATTTTTTTGTAGAG[A/G]TGGGGTCTTGGTATG | 996 |
rs558678489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168409 | TGAGGTCAAAGACCA[A/G]ATATATATATTTCAC | 996 |
rs558689729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47153258 | GAACAGAGGCAGAAG[A/G]GGATGAGAGAGCAAT | 996 |
rs558710770 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47144890 | ACACACACACACACA[C/T]ACATAAATCCTTTTA | 996 |
rs558765347 | in-del | -/AATCA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134238 | TTTACAAGCAAAAAC[-/AATCA]AATCAAATCAAATCA | 996 |
rs558779188 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130911 | ATTAAAAAAGTGGGG[C/T]GAATGAATGTATGAA | 996 |
rs558784130 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166124 | GTGTATACATGTATT[C/T]TTAAGGAATAGTGGC | 996 |
rs558815409 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168983 | TACTTGTTCTTTTTC[-/T]TTTTTTTTTTTCTTT | 996 |
rs558830517 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137675 | ACCAGGGACAGAAAC[G/T]CTGTGGGCTAGTTTA | 996 |
rs558932375 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47180059 | CTTCAGTCCAGGAGT[G/T]CAAGGCTGCAGTGAG | 996 |
rs559021423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136305 | TGTAACTACTACTGC[A/T]AAATGAGACATAATC | 996 |
rs559081453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172214 | CAAATTTGAATTATG[A/G]AGAAACGGTTTGCTT | 996 |
rs559103133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47188401 | AGCATACCCTGGTGT[A/T]AAGGCAGTGAAATGG | 996 |
rs559126451 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47129837 | TGATAATCAATAGTC[C/T]ATCTTTAGAGCAGAT | 996 |
rs559207105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47150957 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGT | 996 |
rs559212170 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117924 | CAACTTGATTATAAA[C/T]TGCTTTCAAAAGTAA | 996 |
rs559219802 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47163916 | TTACAGGCTCGTGTC[A/C]CCACGCCCAGCTGAT | 996 |
rs559254478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47139138 | CATGAACTCTGAAAA[A/G]GAAATTTGAGTTTCT | 996 |
rs559306020 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159594 | CGGGGACAATCGAGA[A/G]TTTGGCCAGGATGTT | 996 |
rs559481223 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118950 | CCAGAAAGACTCTCA[C/T]CTCTGGCACATAAAT | 996 |
rs559535799 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118964 | ACCTCTGGCACATAA[A/G]TTCCTGCTACAAAAA | 996 |
rs559575789 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47147129 | TAGGCAGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 996 |
rs559607194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140003 | AAAAAAGAAAGGAAA[A/G]GAAATTTTCACAGTT | 996 |
rs559640096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47125789 | CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 996 |
rs559646494 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47129954 | TCACATTTCATCAGG[-/T]TTATGCGGTCTTTCA | 996 |
rs559650606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124579 | GTGAGCCACCATGCC[C/T]GGCCCAGTGATTTAT | 996 |
rs559655577 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47162172 | CACTGACTCCTTCTT[C/T]TTCTCCTCTGACCTT | 996 |
rs559686000 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133163 | ATTTTTTTGAGACAG[A/C]GTTTTGCTCTTGTTG | 996 |
rs559687285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178747 | AATAAGGCTCAGAAT[A/G]ACTTTTGGCTTAAGA | 996 |
rs559726456 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47132566 | TTTACTTATTTTTAA[A/T]TAAAAAAATTTTTTT | 996 |
rs559800572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143155 | TTTTTTCAGAGATGG[A/G]GTCTTGCTATGTTGA | 996 |
rs559826602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47169490 | TGTCTACCAAAAATA[C/T]AAAAATTAGCTGGGC | 996 |
rs559844735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47146236 | CTTTCCTGGACTCTG[C/T]GAGGTGCTCTAGCAA | 996 |
rs559863888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47142751 | AATTCTCAGCTCACC[A/G]CAACCCAACCTCTGC | 996 |
rs559891891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168793 | AATAATGTATTCTGT[C/T]CAGAAATACATTTTC | 996 |
rs559933325 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120108 | TGAACTTAAGGGGTT[A/G]TTAAGGGCCTTGTTT | 996 |
rs559952122 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47128484 | CATAATTTGAAAAAG[A/G]GTGAGAAGTAAAGAG | 996 |
rs560046288 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120782 | TGCCTTTCATTCTGT[A/G]TACAGTCAGGGTCCA | 996 |
rs560116209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158072 | GATTCTAACTTATTT[C/T]TTATTCTCAATTTTA | 996 |
rs560142566 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140148 | ATAGCTTAACGATTT[A/G]TAACTTCCTTGCAAT | 996 |
rs560199914 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142806 | GCTTCAGCCTCCCGC[A/G]TAACTGAGATTACAG | 996 |
rs560233079 | in-del | -/ATTTTTGT | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47128197 | CACCATGCCTGGCTA[-/ATTTTTGT]ATTTTTGGTAGAGAT | 996 |
rs560281564 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47154988 | TAAAAAGCTATCAAA[A/C]AAGGAACTAAACTGA | 996 |
rs560291021 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190391 | CTCCCCTTCTCCCCC[A/C]AAAAAGAGTGAACCA | 996 |
rs560312576 | in-del | -/TGGTG | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47126563 | ATCATAGTCCAGACA[-/TGGTG]ACTGATGAGATTAGA | 996 |
rs560397041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174356 | TGGCTGTCTGAAATG[C/G]CATGTTCAGAAAACT | 996 |
rs560541542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47182239 | TATTGGAATGCAAAT[A/G]AGTAAAGTTATCATA | 996 |
rs560629844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47156088 | CCATAAAGACAGTAT[C/T]TTTTAATGTGTTTAC | 996 |
rs560658143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156541 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 996 |
rs560675971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134648 | ACCCAGCTAATTTTT[G/T]TATTTTTAGTAGAGG | 996 |
rs560702838 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47183179 | GATCATGATACAAGC[A/G]TTATTTTTTATTTTT | 996 |
rs560715539 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47137482 | GGAGGAGCTTCAGTA[G/T]ATACTCAATTCTAAT | 996 |
rs560729996 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134308 | TAAACCCATATAGAT[-/T]TTTTTTTTTTTTTTA | 996 |
rs560753796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148738 | TTCTTGTCAGAAACA[A/G]TATAAGCCAAAAAAC | 996 |
rs560761256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164662 | TCTCTACTAAAAATA[C/T]AAAAATTAGCTGGGC | 996 |
rs560814743 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47148152 | GTGCAGTGAGCCAGA[C/T]TGTGCCACTGCACTC | 996 |
rs560914443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47131074 | CTAAATACTAGTTCC[C/T]GAAAAGAGAAAAGCT | 996 |
rs560948174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160353 | ATGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 996 |
rs560963947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176853 | AAATGATACATTATT[A/C]CACATCTTTAGTAGA | 996 |
rs560990444 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126245 | GAATGACACAGCCCC[A/C]GGAGATCCTGAGAAC | 996 |
rs560995930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178834 | TTGAGACGGAGTCTC[A/G]CTCTGTTGCCCAGGC | 996 |
rs561026212 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47152331 | AAAAAAATAATAATA[C/T]GATAAGATTTTATAC | 996 |
rs561132120 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159507 | GCACCAGCACAGAGC[C/T]GCAGTGGCCTGTCAC | 996 |
rs561139360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184475 | AAAATTTCACACACA[C/T]ATACTAAAGTCAAAA | 996 |
rs561274839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176003 | CTCATTTTTTTTTCA[C/T]CCGGTAAGGACTATG | 996 |
rs561276703 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47185240 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 996 |
rs561281466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47123062 | CTTCCTACAGATGAA[C/T]TCATACCAGCTTTTG | 996 |
rs561288731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168061 | CAGGCAAGCCACCTG[C/T]CAGGAACCTCCATGT | 996 |
rs561346000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47151649 | ACTCAACTCAAAATT[A/G]CATTAGTGTTGTAAG | 996 |
rs561376334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47130116 | CCTGTAATCTGAGCA[C/T]GTTGGGAGGCCAAGG | 996 |
rs561464177 | in-del | -/GATGATGAT | 0.106633 | 0.204807 | intron-variant | CDC27 | GRCh38.p7 | 17:47135408 | TCATGGCCATAACTA[-/GATGATGAT]GATGATGATGATGAT | 996 |
rs561513070 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119170 | TAATACAATAGCATA[C/T]GTGTTAGAATCCAAG | 996 |
rs561594897 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CDC27 | GRCh38.p7 | 17:47161876 | TTCCTAAGTAAAGCC[A/G]TTCCCTCAGGCCTCA | 996 |
rs561665070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47129139 | GATAACTTTAAGATA[A/G]CTACCTGATGAAAAA | 996 |
rs561670374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156146 | TTAAATTTTCCTCCA[A/G]TTTTTTTTTTGAGAT | 996 |
rs561673660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172376 | CTTTAAACAGACTAC[C/T]AGTAAAGGATCTTGT | 996 |
rs561710471 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47147166 | AGCACTTTGGGAGGC[C/T]GAGACGGGCGGATCA | 996 |
rs561721895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47180161 | TACAGCAAAATATGG[G/T]GCCTGCCTAGGTATC | 996 |
rs561734320 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189300 | GGAGGCCGAGCGATT[A/G]CCGAGTGCTTCCGAG | 996 |
rs561758500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47133589 | GGATTACAGGCATGC[A/G]CCACCACACCCAGCT | 996 |
rs561797867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47156702 | ATCTGCCTGCCTTGG[C/T]CTCCCAAGGTGCTGG | 996 |
rs561833893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140083 | CAGAAAATAAGAGCA[C/T]TTTAAAACTGAGTGC | 996 |
rs561843648 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176478 | AGTATTTTAAAACCA[C/G]GCTTAGAGTAAAAAG | 996 |
rs561848041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47139509 | CCTGACCTTGTGATC[C/T]ACCCGCCTCGGCCTC | 996 |
rs561962378 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118346 | ACAGAAAATGTAGGG[A/G]CCACCTTTCATTCTT | 996 |
rs561980251 | snp | A/C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171016 | TGAGATGGGAGGATC[A/C/G]CTTAGGCCCAGATGG | 996 |
rs562078492 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47155147 | ATGTCTCTAGAGACC[A/G]TTAGATAACTATAAC | 996 |
rs562124864 | in-del | -/TTTC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125924 | TCAGAATTGATATGT[-/TTTC]TTTCTATGATTGCAT | 996 |
rs562213487 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47123936 | GAACAATTTGTTTCA[A/G]TTCTTCAAGTTCTTG | 996 |
rs562234064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136548 | CAGTAAGTATGGTGT[C/T]GAGGCAGAAATAGGA | 996 |
rs562283941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179202 | AATTTGACTTACAGA[A/G]GATCCTACTGATCAA | 996 |
rs562285992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47169561 | GAGGCAGGAGAATTG[C/T]TTGAACCCTGGAGGT | 996 |
rs562308574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47151213 | AGGATTAGACTTACC[A/G]TTCTGGGAGCATTAC | 996 |
rs562323523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47125681 | CCCAAGTAGCTGTGA[C/T]TACAGGCGCCCGCCA | 996 |
rs562324410 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47149136 | GTAAAAATATTGTTC[-/A]AAAATAAAGATGAAA | 996 |
rs562349250 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151481 | TAATCTGTTTATAGA[C/T]ATGCATAATGTGGGG | 996 |
rs562551386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47121801 | TTGGAGTGCAATGGC[A/G]TGATTTCGGCTCACT | 996 |
rs562603775 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47125568 | AATCTTTTTTTTTTT[-/C]CCCTGAGATGGAGTT | 996 |
rs562611358 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47182930 | ACTCAGAAGGCTGAG[A/C]TGGGAAGACTGCTTG | 996 |
rs562685760 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47175820 | GACTCTGTCTCAAAA[C/G]AAAAAAAATAAAACA | 996 |
rs562696207 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187702 | CTGGGGCCAGAGAAG[C/G]CAAAAAAAAAAAAAT | 996 |
rs562742361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47182435 | CCCTGTGTGTTCCTT[A/G]TTGATACCAAAACCT | 996 |
rs562781296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47150515 | CCTGGGGTTATCAGA[A/C]GCTGGAGGAGGCAAG | 996 |
rs562844505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158936 | TTTTGTATTTTCGTC[A/G]AGATGGGGTTTTGCC | 996 |
rs562956077 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47188329 | ATGACTTGGCACCGC[A/C]TCACACACTTAAAAT | 996 |
rs562997210 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120804 | CAGGGTCCAATGAAA[A/G]TGGCACACTCATGGT | 996 |
rs563036202 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47128343 | GCCCTGAATTTATTT[G/T]AAAAGATTTTGCTTC | 996 |
rs563064091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148779 | ACATCCCTAAAAAAA[C/T]TGTCAATTAGAAATT | 996 |
rs563084016 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47187654 | GGTGGTTATAGTCTA[C/T]CAATGCAACTAGTTT | 996 |
rs563130520 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137876 | TGTGATCTTGGCTCA[A/G]TGCAACCTCCGCCAC | 996 |
rs563164697 | snp | G/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142367 | TTATTCCTCCTTTAT[G/T]AGTTTTACTTTTTGT | 996 |
rs563272101 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47125742 | AGAGATGGGGTTTCA[A/C]CATGTTGGCCAGGCT | 996 |
rs563278256 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142915 | TCCTGACCTTAGGTG[A/G]TCTGCCTGCCTTGGC | 996 |
rs563294477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132462 | GAACAAGTATAGAAT[C/G]TGGCATTTTAATAAT | 996 |
rs563297170 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47160375 | TGGGATTACAGGTGC[A/T]CACCACCATGCCAGC | 996 |
rs563316788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124811 | GAAAAAGGTAAATAA[C/T]GTCAAGATATTATTG | 996 |
rs563408015 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47135093 | ACTTGCTTAAAGTTA[C/T]ACAGCTAATAAAGAT | 996 |
rs563565072 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47139017 | GGTTTTTATGTGAAT[C/G]AGTATTAACACAAGG | 996 |
rs563573663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47187521 | TGGCCAGGCAGGTCT[C/T]GAACTCCTGACCTCA | 996 |
rs563611199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152974 | TCTATCAGCAGGTCA[C/T]ATTTTTTCCTCTATG | 996 |
rs563666648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168193 | TCTTATCACCAATTT[A/C]ATGGTGAAACTTAAT | 996 |
rs563697468 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47166240 | TGTTTTCTGGAAGAG[A/T]TTATGTAGCATTAGG | 996 |
rs563697546 | snp | A/G | 7.2102e-05 | 0.00600381 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156917 | GTTTGACTTACCTTG[A/G]GGTTAATGGACTAAG | 996 |
rs563718888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47186294 | TTGAATCCATGTTAG[A/G]TGCTGTCCCTGAACA | 996 |
rs563721748 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47177918 | AGTTGCATTAATGTA[-/T]TTTTTTTCCTCATAG | 996 |
rs563862838 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47130878 | GCGAAACTCCATCTC[A/C]AAAAAAAAAAAAATT | 996 |
rs563896078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176973 | GAGTTTGGGCTCTCA[A/G]TATCCTGGTTAATAG | 996 |
rs563908224 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47185271 | GCAAGCTCCACCTCC[C/T]GGGTTCACGCCATTC | 996 |
rs563928946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47130221 | AAAAAATTAGCCGGG[C/T]GTGGTGTCACACGCC | 996 |
rs563959388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127216 | TTCAGTGAGCTATGA[C/T]TGCACCACTGCACTC | 996 |
rs563961323 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47134611 | CTCCCAAGCAGCTGG[C/G]ACTACAGGCACGCAT | 996 |
rs563979572 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182740 | ATCAAAATCCAAAAT[-/G]TATTTTATCTATTTT | 996 |
rs563997078 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178470 | GGCCTGGGAGGTCAA[C/G]GCTGAAGTGAGAAAA | 996 |
rs564007493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141788 | CCTTCTTAAGCATGG[A/G]CATTTATTTTAATGA | 996 |
rs564044837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47123093 | AGTTCCTTTTAATAT[A/G]ATCAGACATTATTTT | 996 |
rs564070856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148889 | TTCAAGACTAGCCTG[A/G]CCAACATGGTGAAAG | 996 |
rs564073923 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47127672 | TCCCAAAGGGCTGGG[A/T]TTACATACGTGAGCC | 996 |
rs564101977 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47165985 | TTTTTAATTATTTTG[C/T]GTATGTTCCCACAAG | 996 |
rs564124762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47173736 | TAGCTTTTTGAAGCA[C/T]AGTAACTTAAAAATT | 996 |
rs564545381 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190275 | TACCTCTCTGAACTT[A/C]TGTTCGCTTAGTTTG | 996 |
rs564570928 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139076 | CAAATAGTGATGTAA[C/G]CATATTGACAGTCAA | 996 |
rs564593461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47130981 | ATGTGAGAATAGGTA[C/G]TGCCAACGTCTGCTT | 996 |
rs564604928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47147617 | GTGGCTCATGCCTGT[C/T]GGCCCAGCACTTTGG | 996 |
rs564660961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47154403 | TAAAAATATGATTAT[A/G]TTTATTTAACTATAT | 996 |
rs564695716 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145398 | TAGAGTCTTCAGTTG[A/T]AAATTGATCAGTGTA | 996 |
rs564714667 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117828 | CATTGCTCTAGTTTT[C/T]TGTGAAACATAAAAC | 996 |
rs564718671 | snp | A/T | 7.49738e-05 | 0.00612219 | intron-variant | CDC27 | GRCh38.p7 | 17:47172084 | AAACAGACATTTTTT[A/T]AAAAGGCTATTGTTC | 996 |
rs564836995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47137442 | ACTAAAATCAAGCCT[C/T]AACTTAGAACAGAAA | 996 |
rs564850080 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151748 | CTGCCTAAATTAAAG[A/G]AATGTAAAGAATCAA | 996 |
rs564868450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136772 | TTTTTTCCTATTATC[C/T]AATAAGTGAATTATG | 996 |
rs565029200 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47150549 | AAATCCTCCTCTAAA[C/G]ATTTTGGAAGGGGAA | 996 |
rs565029261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159536 | ACCTTGCAAGGGACG[A/G]CGTAGGGCTTGCCAA | 996 |
rs565155921 | snp | A/C | 2.10099e-05 | 0.00324107 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120907 | GCACTAGTCACACAT[A/C]CAGTTGTAAAAGTCT | 996 |
rs565178319 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163361 | CAGGATTGGGGTAGG[A/G]TTGTTCCACTTTCAA | 996 |
rs565228744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47122875 | GACAGGGTTTTGCCA[C/T]GTTAGCTAGGCTACT | 996 |
rs565273552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176781 | GTTTGATGTGTCTGT[C/G]AAACATCCAAGTTAA | 996 |
rs565280738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175954 | TCAACCTACTAGCTA[A/T]GACTTAGGGCAGAGT | 996 |
rs565298023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47129025 | ATCCGCCCGCCTTGG[C/T]CTCCCAAAGTGCTGG | 996 |
rs565411334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47121864 | CCTGTCTCAGCCTCC[C/T]GAGTAGCTAGGATTA | 996 |
rs565444452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143067 | GCCTTGACCTCCCCA[G/T]GCTCAAGTGATTCTC | 996 |
rs565514382 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47169745 | AGTAAGGATAAGTGG[A/T]GAGTTCAAACTTAGA | 996 |
rs565521236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178962 | CATGTGCCACTACAC[C/T]GGCTAATTTTGTATT | 996 |
rs565543351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178307 | TTGGGAGACGGAGGT[A/G]GGAGGACTGCTTGAG | 996 |
rs565548937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47161736 | GCCTGGGTGACAGAG[C/T]GAGACTCTGTCTCAA | 996 |
rs565575537 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158906 | ATTACAGGTGTGAGC[C/T]ACCGCACCTGGCCTT | 996 |
rs565582634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47187549 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 996 |
rs565616734 | in-del | -/A | 0.287033 | 0.247242 | intron-variant | CDC27 | GRCh38.p7 | 17:47157396 | TCACCTGTGAAGACA[-/A]AAAAAAAAAAAGTTT | 996 |
rs565656902 | in-del | -/CTAT | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47135597 | AAAACAAAAGAAAGG[-/CTAT]CTATTTTGTACTTAG | 996 |
rs565667274 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168026 | GGGGAAAGAGAGGTG[C/T]GGAGCTTCCATGGCC | 996 |
rs565668569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47162900 | TAGATATATGTATAA[A/C]TCACATAAGAGCTAA | 996 |
rs565678808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47170518 | AAATTTTTTTTAATT[A/G]CAATAGTGGCAAACA | 996 |
rs565803307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47186906 | CGCAATCTGTCATCA[G/T]AGTTTTTTTTTTAAT | 996 |
rs565820050 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | CDC27 | GRCh38.p7 | 17:47140681 | ATAAATTAGAAATAA[-/T]TTTTTAAATGGCTTT | 996 |
rs565857189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124315 | TTGAGGTGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 996 |
rs565858046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47169303 | GCTATCTTTTCTTCT[A/G]TCTCCTCAGTGGATC | 996 |
rs565858655 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153824 | GCAGTGACTCATGTT[C/T]ATAATCCTAGCACTT | 996 |
rs566015503 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130256 | GTCCGAGCTACTTGG[G/T]AGGCTGAGGCAGGAG | 996 |
rs566021718 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47125043 | CTGCCTCAGCCTCTC[A/G]AGTAGCTGGGATTAC | 996 |
rs566027840 | in-del | -/AAT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47152321 | TTATACACAGAAAAA[-/AAT]AATAATACGATAAGA | 996 |
rs566086913 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47145003 | ACACACAACCTTTCT[C/T]GGATGATTTAGCTAA | 996 |
rs566144367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47131527 | GAAAAAAAGAGAGAA[A/G]CTGAGGGGAGGGAGA | 996 |
rs566149935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138449 | AATTTTTTCAATCTA[C/T]GTAACTTCTGCTCAA | 996 |
rs566153705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160361 | GCCTCCCGAGTAGCT[A/G]GGATTACAGGTGCAC | 996 |
rs566155094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148958 | ATAGCACATGCCTGT[A/G]ATCCCAGCTACTCGG | 996 |
rs566251945 | snp | C/T | 1.72157e-05 | 0.00293386 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157104 | TGAATTGGAAGATTC[C/T]AAATTCAATCTGTTT | 996 |
rs566269092 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47153156 | TGTACACTGCACTCA[A/G]TACCTGGTTTGATAT | 996 |
rs566331027 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135170 | AATGCTATTCCCACA[C/T]TTCTGTTTTATATTA | 996 |
rs566529115 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117718 | TTGTTTTTGTCATAG[C/T]ATTTATTTTGATATT | 996 |
rs566631260 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47141344 | GGCTTTAGGTTAATC[A/G]TTCTCTCCTTTTCTG | 996 |
rs566674033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47164887 | TTAGCAGTTTTTACA[C/T]GTTTATATAGAGAAT | 996 |
rs566744943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172639 | GACAGACTATAGTAA[C/T]AATAATTAAATTACA | 996 |
rs566862928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184048 | ACCTACATGTTTAAT[C/T]TTGCTGTAAGTGAAA | 996 |
rs566879032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164208 | AGCAATAGGTTATAC[A/G]ATATAGCCTAGGTGT | 996 |
rs566913477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47139720 | TATAAATCCTATTGA[G/T]CCCTGAATATACACA | 996 |
rs566941753 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157678 | AAAGCTGAAAATAAC[C/T]AGATCTCATTTTTCT | 996 |
rs566982739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47173815 | ATAATGAAACTGGCC[A/G]GGCGTGGTGGCTCAT | 996 |
rs567040817 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140476 | AATATAGGTAGGTAC[A/C]TTTTGGTTTCAAAGT | 996 |
rs567048716 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189029 | GGCAGGACACGGCAG[C/G]AGGGGAGGCGGGAGA | 996 |
rs567053197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47133205 | GTGCAATGGTGCAAT[C/T]TCGGCTCACCACAAC | 996 |
rs567073588 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144771 | TACCTGAGTCTGGGT[C/T]AAAGAATTTCAGAAA | 996 |
rs567090210 | snp | C/T | 0.000556066 | 0.016665 | intron-variant | CDC27 | GRCh38.p7 | 17:47129557 | GTTAATACTCCCTCT[C/T]GATATTTATGAAGAA | 996 |
rs567138068 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189528 | ACGCCCAATCGGCCG[C/T]CCCAGGGTTGGGCTA | 996 |
rs567173827 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47141698 | ACACAAGAAAGAACT[A/G]TATCTATAAATTATA | 996 |
rs567259274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47168342 | GCTACCAGTCAATTC[A/G]TTTGCATACAAAAAG | 996 |
rs567271772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47177229 | TGTTTGAGGCCAGCA[C/T]GGGCAACATAGGGAG | 996 |
rs567380989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159741 | GGGTCTGCTTCTGCA[A/C]CGGCATAATCTTCAA | 996 |
rs567413119 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47185463 | GCTGGGATTACAGGC[A/G]TGAGGCACCGCGCCC | 996 |
rs567417932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136199 | ATATTACAGAGAACA[C/T]AGCTATCGGAAGAGA | 996 |
rs567448286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47136821 | CCAAGCACTTTTCAT[C/T]CCAATCACCATTTCG | 996 |
rs567526590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174782 | CCAACATGGTGAAAC[C/T]CCATCTCTACTAAAA | 996 |
rs567531675 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47145531 | TTATTCATTATGAGC[C/T]CCTGGGACCGTGCCT | 996 |
rs567568261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47167260 | TTTTCAACAGAGTAA[C/T]ATTTATAATACTTCA | 996 |
rs567614669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47149848 | TAATCCCAGCTACAT[G/T]GGAGGCTGAGGCAGT | 996 |
rs567645672 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145540 | ATGAGCTCCTGGGAC[C/G/T]GTGCCTGAATTTATG | 996 |
rs567660991 | in-del | -/TA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124613 | TTAACGAAAAATAAC[-/TA]TATAATTTTTCAGAA | 996 |
rs567665132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158574 | CAGATACTAGAGTTA[C/T]TGAGGGAGATGTGAA | 996 |
rs567734625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128636 | AGAGAGTACTAGATA[G/T]TAGGCCCCTCAAAAG | 996 |
rs567738225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143614 | ATCACTGATCTGTTG[C/T]CCATTCCTATAATTT | 996 |
rs567758205 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122178 | GATAAAACAGTACTG[A/G]TTACATATTCAAACA | 996 |
rs567788506 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149584 | GATATCAGATCGCAA[C/T]CTGGATCTATAGAAG | 996 |
rs567790512 | snp | C/T | | | intron-variant, utr-variant-5-prime | CDC27 | GRCh38.p7 | 17:47188773 | CACACAAGCTCCGAT[C/T]AAATGTGCTTCTCGA | 996 |
rs567800702 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47150807 | GGAGGCTGAGGCAGG[A/C]GGATCACCTGAGGTT | 996 |
rs567902964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47170838 | CGGCACAGTGGCTCA[A/T]GCCTATAACCCCAGC | 996 |
rs567915553 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179482 | GATTACTAGTTACCG[A/C/T]CTGTGGACATTAGTC | 996 |
rs567915713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47170122 | CTTCATTACCAAAGT[A/G]CATCTAACTATGGAG | 996 |
rs567978995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166598 | TTTGCAATTTCACTG[A/C]TTTCTACTTTTTATT | 996 |
rs568014212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147354 | CAGTGAGTCGAGATC[G/T]CGCCACTGCACTCCA | 996 |
rs568066102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164011 | TCAGGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 996 |
rs568077756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138554 | TTGTGATTTTTCTAT[C/T]TGTGAATCTGCACCA | 996 |
rs568139454 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47140699 | TTTAAATGGCTTTTC[C/T]GAACACAGCTCTTGC | 996 |
rs568202961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147804 | TACTCAGGAGGCTAA[C/T]GCAAGAGAATCGCTT | 996 |
rs568245085 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130285 | AGAATTGCTTGAACC[C/T]GGAGGCAGAGGTTGC | 996 |
rs568270748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47125874 | CTCTAAGATGACACA[C/T]TCCAATCCTCCTTCA | 996 |
rs568391537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47137925 | CCTGTCTCAGCCTCC[C/T]GAGCAGCTGGGACCA | 996 |
rs568391611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47146412 | TGCTAAGTTTGGGTA[A/G]TTAGCATCAGAATTA | 996 |
rs568399027 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117248 | GAACCTTCATGAACC[A/G]TAAGTTGTCAGCTAA | 996 |
rs568424556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47125132 | CTAAAGTTGCCCAGG[C/T]TGGTCTTGAACTCCT | 996 |
rs568440184 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | CDC27 | GRCh38.p7 | 17:47123197 | GGATTAAATGGATTA[-/T]AAACTGCTTAATTAA | 996 |
rs568509806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132070 | ATGAAGTGACTTGTG[C/T]AAGGGATAAGGGCAA | 996 |
rs568512013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152509 | TTCCCTTGGAGAAAA[A/G]AAAATCTTTGCTTGG | 996 |
rs568573032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160554 | CTTTTAAATAGGAGG[A/G]TGGAAGGGGTTAGTG | 996 |
rs568606502 | in-del | -/TGT | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47126564 | TCATAGTCCAGACAA[-/TGT]CTGATGAGATTAGAA | 996 |
rs568748462 | in-del | -/TA | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47187816 | TAGGCCTTAAAAAAT[-/TA]TATATATATATAATT | 996 |
rs568790652 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47142784 | CCCGGGTTCAAGCGA[G/T]TCTCCTGCTTCAGCC | 996 |
rs568822118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47183930 | ATAAAGAATCTCTGG[A/G]AGTCTCTATTGAAAG | 996 |
rs568832999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184591 | GTATCATATTCAAGA[A/G]TTGTATCCATTTCTG | 996 |
rs568854269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47142103 | AAAGGTAATTACAAA[C/T]TAATCTATTAAAAAT | 996 |
rs568907518 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47175399 | TGATAAACTATACAA[A/C]TATCAGAGAAGCCCT | 996 |
rs568912314 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130927 | GAATGAATGTATGAA[C/T]GTGGCTGCAGAACTT | 996 |
rs568935180 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119320 | TCTCTCTGGCACCTG[A/G]TACCTAAAGACCCTG | 996 |
rs568978686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128738 | TGAATAATGCACACA[A/C]ATTCGTTTTCTTTTT | 996 |
rs569011835 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149531 | AAAAAAAAAAAAAAA[-/G]AAATGTTAAAAAGAA | 996 |
rs569097793 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47149720 | AGCACTTTGGGAGGC[A/T]GAGGCGGGTGGATCA | 996 |
rs569264718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174568 | GACTCCATTAAGTCA[C/T]TCTTAAAGTAATATT | 996 |
rs569266666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164904 | TTTATATAGAGAATA[C/T]TATCACATTTACAAA | 996 |
rs569276352 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47174057 | CGAGATCGTGCCACC[A/G]CATTCCAGCCTGGGT | 996 |
rs569281349 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47156336 | GTAGAGACGGGGTTT[C/T]GCCATGTTGGCCAGG | 996 |
rs569289800 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120163 | TATCATCTCTGAATG[C/T]TAAAGGTGATCCCAC | 996 |
rs569328695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47180692 | GAAACAAAACATACA[C/T]TATCAGTGGTGTTTA | 996 |
rs569336763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47133810 | TTGGAGTGCAGTGGT[A/G]CAATCTCAGCTCACT | 996 |
rs569410236 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190484 | AGTCAGGAGCTCTCT[A/T]GGCTAGATGTGAGAA | 996 |
rs569439441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141271 | TTAAGTTGGGGGTGG[A/T]GAAAATGCTTTGGGA | 996 |
rs569495607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127386 | ATTTAATCCCTTTGT[A/G]TATCTTTATTAGCCT | 996 |
rs569582334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134362 | CGGGCTGGAGTGCAA[C/T]GGCGTGATCATAGCT | 996 |
rs569664457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160765 | AATGTATACATCATC[C/T]GTTTATGTGCGGAAT | 996 |
rs569666329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47169725 | GGGCAGCTGTAGCTA[C/T]TATCAGTAAGGATAA | 996 |
rs569678843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47169149 | GTATGTGCCACCACA[A/C]CCAGCTAATTTTTTA | 996 |
rs569730318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159589 | GCGCACGGGGACAAT[C/T]GAGAGTTTGGCCAGG | 996 |
rs569738060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47186778 | AAAAAAATGCAGAAA[A/G]CAGTTCTTCATATTT | 996 |
rs569767264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152604 | TGATCTATGACTATT[G/T]TATCAGTGCACTGTT | 996 |
rs569800893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47161580 | ACACGGTGAAAACTC[A/G]TCTCTACTAAAAACA | 996 |
rs569809565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124135 | AATGCATACTTATAT[A/G]ACAATAGGTACTAAG | 996 |
rs569818316 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119317 | ATATCTCTCTGGCAC[C/G]TGATACCTAAAGACC | 996 |
rs569823557 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178223 | GAAAATATTAGAGTG[A/T]ATCATATCTAATAAG | 996 |
rs569879918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47185766 | GACAATGTAAGAAGA[C/T]ACAAAGAAAAAAATC | 996 |
rs569883155 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168457 | CTTTTGTTTACTGTT[C/T]CTCTTCTCCTACTCT | 996 |
rs569905906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47167566 | CATTTGAACAATATA[A/G]TGCTCAAATTTTATG | 996 |
rs569920231 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133462 | TTTTTTTTTTGAGAC[A/G]GAGTTTCGCTCTTGT | 996 |
rs569924636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166737 | AGTGCTATAAATTTC[A/G]CTGTAAGACTTTAGC | 996 |
rs569955700 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161837 | ATGACCATTTCTTCA[-/T]TTTTTTTTTTTTTCT | 996 |
rs570010885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47131336 | ACTGTCAACTTTTTT[C/T]TCTTGCCCTGTCTTA | 996 |
rs570042893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47159217 | CCACAGCTGGAGCCC[A/G]GGTCCTCTGTACGGA | 996 |
rs570049432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47150951 | GCAGGAGAATCACTT[A/G]AACCCGGGAGGCGGA | 996 |
rs570134030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47156243 | TCCCGGGTTCAAGTG[A/G]TTCTCTTGCCTCAGC | 996 |
rs570145229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136985 | AGAGTTTGTTAAAGA[C/T]GTACATTTCATAAGA | 996 |
rs570165050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176063 | TTAAATGACTTAATA[C/T]ATGCACAGCAATTAG | 996 |
rs570175208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47122368 | TGGTTAGAAAAATAA[A/G]ATAAAAGAGTAGCCT | 996 |
rs570307676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164097 | CATATTTCTACTGTA[C/T]CTTTTCTTTGTTTAG | 996 |
rs570319905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47163078 | ATTGAGTGATACACA[C/T]AAAACCCAGCCAGAA | 996 |
rs570374116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147927 | AAAAAAAGGCTGGGC[A/G]CGGTGGCTCACACCT | 996 |
rs570443794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155532 | ATTACAGGCATGAGC[C/T]CCCATGCCCAACCCA | 996 |
rs570494562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132870 | GACCTCCCAGGCTCA[A/G]GTGATCAATCCTCCC | 996 |
rs570499333 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143731 | AAGGACTAATTAACT[C/T]CACAAAAATCATAGA | 996 |
rs570530294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134460 | ACTACAGGCATACAC[A/C]ACCATGCCTAATTGT | 996 |
rs570550613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172502 | TATGAAATAATTTCT[A/G]TATTTTAAAAAGACC | 996 |
rs570564733 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140075 | GAGTATGACAGAAAA[C/T]AAGAGCATTTTAAAA | 996 |
rs570571736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47141297 | TGGGAAGAACTAAGG[A/G]GTAATATAAATTGGG | 996 |
rs570612147 | snp | C/G/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120609 | ATTTTCCATATCTAA[C/G/T]GGTTCCTTCAAGATA | 996 |
rs570760104 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168602 | AATGAATCTCAAAGT[C/T]TCTTGACTAAATGAC | 996 |
rs570778757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47132142 | GGGTGTAATAGGCTC[C/G]AGAATACTGTTTCAA | 996 |
rs570831555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47170973 | AGGTGTAGTGACACG[C/T]GTCTGCAGCTCCAGC | 996 |
rs570839271 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47182277 | CTTTTAATTTTTTGA[-/AT]ATATGTTTTCTCTTT | 996 |
rs570881018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47126622 | TGATTTATGTGGCCT[A/C]TCTGGTAGGTATGTT | 996 |
rs570899284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47180343 | CCCAGATCTTCCTCA[C/G]TTTTCTCACTGAATT | 996 |
rs571052278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47130245 | ACACGCCTGTAGTCC[A/G]AGCTACTTGGGAGGC | 996 |
rs571115139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47188070 | AAAATGAAATAAATA[C/T]GAAAGTAGTGATATA | 996 |
rs571175712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128781 | TTTTAATTTTTTTTT[A/T]TTTTTTTGAGATGAA | 996 |
rs571205698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47176387 | TGTTTATCTTTTCTA[C/T]ATTTATTTACATCCT | 996 |
rs571212472 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47135605 | AGAAAGGCTATCTAT[C/T]TTGTACTTAGAATAA | 996 |
rs571224745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47177018 | CTGAACGTTTTACTC[A/T]GGTTCAGTTCTCTCC | 996 |
rs571247725 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47185442 | CCTGCCTCAGCCCCC[A/C]AAAGTGCTGGGATTA | 996 |
rs571287153 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139266 | CATTACAGAATAACT[-/C]TTTTTTTTTTTTTTT | 996 |
rs571291123 | in-del | -/GAT | 0.0232913 | 0.105372 | intron-variant | CDC27 | GRCh38.p7 | 17:47135410 | TGGCCATAACTAGAT[-/GAT]GATGATGATGATGAT | 996 |
rs571291402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47167671 | TCTTAACAGTAACAA[C/T]CATCAATACAGAAGA | 996 |
rs571434110 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CDC27 | GRCh38.p7 | 17:47136160 | AAACAAACAAACAAA[A/C]AAAAAAAAAACTGAG | 996 |
rs571497356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143263 | GCCACTGCGTCCGCC[A/G]GGTCTCCAGTTTTTT | 996 |
rs571524718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184002 | AATTACCACCAAATT[A/G]CTCCTTTATGAAATC | 996 |
rs571592472 | snp | A/G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150935 | TACTCAGGAAGCTGA[A/G/T]GCAGGAGAATCACTT | 996 |
rs571619490 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156339 | GAGACGGGGTTTCGC[C/G]ATGTTGGCCAGGATG | 996 |
rs571662114 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166518 | TTTGGGGTCACTTTC[A/G]GCAGTTTTACCAATC | 996 |
rs571689174 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47147139 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 996 |
rs571714334 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186198 | CTCTGCTCAAAAACT[C/T]TTCTGCTCATATAAT | 996 |
rs571791692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47181755 | TTTAAGTGATAAAAC[C/G]CCAATGCCCACAGAG | 996 |
rs571849542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47134954 | CAGCTAATTTTTACT[A/G]AGTAGTTATTACATG | 996 |
rs571851231 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47127455 | TTGCCCAGGCTGGAG[C/T]GCAGTGGTGTGATCT | 996 |
rs571880831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47184829 | ATGATGAACAGGGCT[A/G]AAATCAGCACCTCTG | 996 |
rs571887387 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119492 | TACAGGTAAGTTTGT[C/G]CTCCATCAAATAATC | 996 |
rs571964000 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47134536 | CTCACTCTGTTGCCA[G/T]GCTGGAGTGCAGTGG | 996 |
rs572012547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128092 | CTGGAATGCAGTGGC[A/G]TAATCTTGGCTCACT | 996 |
rs572021472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145412 | GAAAATTGATCAGTG[G/T]AGGTGTTTGAGTGTT | 996 |
rs572051699 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | CDC27 | GRCh38.p7 | 17:47147435 | CAAACAAACAAAAAA[A/C]AAAACACTAGGCATA | 996 |
rs572069541 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47145969 | CAGCCTGAGCTCCTC[C/T]GGGAAGGAAATTGAG | 996 |
rs572086187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152827 | TCCAAAACATTACAT[C/T]ATTTGTCCTGCCACT | 996 |
rs572125008 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47187244 | AAACAGGAAACCTGA[C/T]GGGTACTATCTAGAA | 996 |
rs572150417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168434 | TTTCACTATATCACA[C/T]TTACAAACTTTTGTT | 996 |
rs572173321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47177467 | TTATAATCCCAGCTA[A/C]TCAGGAGGCTGATGC | 996 |
rs572206752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47146856 | GATTGCTTGAGGCCA[A/G]GAGTTTGAGAACAGC | 996 |
rs572221258 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128553 | GCTCTCATAACTTAA[A/T]ACACTTTCCCTTTAT | 996 |
rs572260147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159968 | CCACGGCTGCGACCC[C/G]AGCCCTGGATGCCAC | 996 |
rs572284837 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161803 | TGTTTGAGGATTATC[C/G]TAAGCTTCAAATAGG | 996 |
rs572315481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47150248 | AGCAATTGCTAATAA[C/G]GCAATATTGAATTGT | 996 |
rs572332745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47160938 | GCTTCCCACACTTGT[A/G]TAATTTAAGCCAATA | 996 |
rs572372528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47136367 | TTTTAGTAATATAAT[A/G]CTTCAGATTTAGAAG | 996 |
rs572396621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152264 | GTTAAGTACTAAAAA[A/G]TTTTAAGACAGCTAA | 996 |
rs572484642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47181960 | AAAGATCCAGCTTAA[A/G]TAACATCTGCCCCAT | 996 |
rs572537183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47123712 | GCACCATGCCTGGCT[A/G]GGATATCATTTTCTT | 996 |
rs572543432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47180987 | CATGGCATGGTGGCC[A/C]ATGAGTATAATCCCA | 996 |
rs572568252 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47124240 | TATGCAGGTGGTAAC[-/A]ATCCTTGCTTTTGGT | 996 |
rs572575758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47122922 | AGATGATCCACCTGC[C/T]TCCCAAAGTGCTGGG | 996 |
rs572600502 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CDC27 | GRCh38.p7 | 17:47143076 | TCCCCAGGCTCAAGT[A/G]ATTCTCCCACCACAG | 996 |
rs572687183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47143750 | AAAAATCATAGATGG[C/T]CCTCTAAATTAAAAC | 996 |
rs572695833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184345 | TCAATAAATATGTAG[C/T]TTCTGTTGCATAACA | 996 |
rs572701642 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148421 | CAAAAATGAAGAATT[A/T]GTGAGCTGTGGGGCA | 996 |
rs572715704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155671 | TATTAATAGGTGTGA[A/C]AGCTAGGTTCAGTGG | 996 |
rs572735334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135992 | AAAAATACAAAAAAA[A/T]TTAGCCGGGCATGGT | 996 |
rs572737147 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | CDC27 | GRCh38.p7 | 17:47134485 | AATTGTTTTTTTTTT[G/T]TTTTGTTTTGTTTTG | 996 |
rs572790059 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190941 | CTGAAAGATTCAAGA[C/T]GGCTTCACTCACATG | 996 |
rs572879572 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117544 | CAGATCCTGACCTTT[C/T]TAAATAGATTCTAAT | 996 |
rs572889658 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47154011 | GAAGGATCACTTGAG[C/T]CTGGGAGGTAGAGGC | 996 |
rs573090983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47124602 | TGATTTATTTTTTAA[C/T]GAAAAATAACTATAT | 996 |
rs573129806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140919 | TGAAGGGAAGAGTAA[A/C]CTTCCCTCTGAGTAC | 996 |
rs573157280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47162193 | CTCTGACCTTCACAG[A/C]CAATCAGCAACGAAG | 996 |
rs573180762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47163391 | ATACTCAATCTTTTA[A/T]TCTTGATGATGAATA | 996 |
rs573195309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47171202 | AATTCAACAACAAAT[A/G]TCTCAGAAATTTCAG | 996 |
rs573200656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47125646 | CCTCCCAGGTTGAAG[C/T]GATTCTCCTGCTTCA | 996 |
rs573255825 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47154122 | CCTCATGAAACTTGC[A/C]GCAATATTTACTATA | 996 |
rs573341666 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175570 | CCTGTAATCTCAGCA[A/C/T]TCTGGGAGGCCAAGG | 996 |
rs573397883 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177434 | ATACAAAAATTAGGT[A/G]GGCGTGGCCGCAGGC | 996 |
rs573409735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138633 | AGGAAAAAAAAGAAA[G/T]AAGCGTGGGTGACAC | 996 |
rs573433493 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151173 | CAACAGAGCCTCAGG[C/T]AATCACTGCAAGCTG | 996 |
rs573456297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179151 | GAAAGACAAATGGGC[A/G]ACAAAGAACTAGTGA | 996 |
rs573519980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178771 | CTTAAGATCAAATGG[C/T]AAATGAGTATCTGAA | 996 |
rs573546304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179797 | CAGGTACATAAATAA[C/T]GTGGATTAAACAGCT | 996 |
rs573549998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159361 | CATCAAAGGTGGCCT[C/T]GGTGAAGTTGCCCAG | 996 |
rs573557943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47167752 | CATCAAACGCCAGCT[A/G]AATGTCCGCTAATTC | 996 |
rs573561123 | snp | C/T | 0.000193723 | 0.00983993 | intron-variant | CDC27 | GRCh38.p7 | 17:47122669 | AAAATTCTAACTATA[C/T]ATATACTTATTTATT | 996 |
rs573645154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47121693 | CCACCTCAGCCTCCT[G/T]AGTAGCTGCGATTAC | 996 |
rs573695795 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190435 | ATTTTGTTTTTCAGC[A/G]GATGAGGAAACAGTT | 996 |
rs573742384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128991 | TGGCCCGGCTGGTCT[C/T]GAACTCCTGACTCAG | 996 |
rs573855597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175772 | AGTAAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 996 |
rs573959812 | in-del | -/GA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175054 | GAGGAAGGAAGGAAG[-/GA]AGGAAGGAAGGAAGG | 996 |
rs574097826 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47149318 | GAGATCGGGACCATC[C/T]TGGCCAACATGGTGA | 996 |
rs574111157 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117815 | AAAATTAGATAAACA[G/T]TGCTCTAGTTTTTTG | 996 |
rs574140646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166045 | GTTTCAATTTTCTGA[A/G]AAATAGTATTATTTT | 996 |
rs574177834 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47165315 | CCACCAGCAGTGTAC[A/G]AGGAATCCTGCTGCA | 996 |
rs574223889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47142858 | TAATTTTTATTTTGG[A/G]AGAGACTGGATTTCT | 996 |
rs574238352 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180685 | AATGACAGAAACAAA[A/T]CATACATTATCAGTG | 996 |
rs574277056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47157741 | CCATCATATTTTACA[A/G]TAAAGGTTGAAGCCC | 996 |
rs574301179 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47147331 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGT | 996 |
rs574421070 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47125689 | GCTGTGATTACAGGC[A/G]CCCGCCACCATGCCT | 996 |
rs574435832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189074 | GGCCGCACCAGGCCG[C/G]GGAGTGGCCCTACGC | 996 |
rs574446031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47133326 | TATTTTTAGCAGAGA[C/T]GGGGTTTCTCCATGT | 996 |
rs574470182 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47168583 | TGTGTTTAGCTATAA[C/T]GGAAATGAATCTCAA | 996 |
rs574470279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178467 | TTGGGCCTGGGAGGT[C/G]AAGGCTGAAGTGAGA | 996 |
rs574473611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47188310 | CCAGATGTCAGGGGG[A/G]AAAATGACTTGGCAC | 996 |
rs574501428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47146976 | CCTGAAGTGGGAGGA[C/G]TTCTTGAGCCCAGGA | 996 |
rs574557904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47169368 | AACTAACATGGGGCC[A/G]GGTACGGTGGCTCAC | 996 |
rs574615959 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156805 | AATGCCCCTGTTTCC[A/T]CAGTGATTTAGAAGT | 996 |
rs574650296 | in-del | -/AC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177860 | TATATGTGTGTGTAC[-/AC]ACACACACACACACA | 996 |
rs574706979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47153733 | TGCCACAGATATGCT[C/T]TTTAAAAATGGTATT | 996 |
rs574709338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47144086 | ATACATTAATTATAT[A/C]AGTACTCTAAAGTTG | 996 |
rs574812562 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174629 | GCTATGTCCATGTGA[C/T]GAAAAATACAGACAT | 996 |
rs574813824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47187102 | AATTTTCACCTAGTC[A/G]TATCCTAAAACTTTC | 996 |
rs574876533 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47165389 | TTTTAGCCATTGTAT[C/G]TAATGGTGGTTTTTA | 996 |
rs574878759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47174825 | GCCGGGTGTGGTGGC[G/T]TGCACCTGTGATCCC | 996 |
rs574929688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47136490 | TACCTTATCTTGATA[C/T]TTAAACTATTAAGTC | 996 |
rs574964877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47166196 | AAGGAAATGTGGCCT[C/T]ATGAGTAGAGGAGTA | 996 |
rs574990904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152023 | CAATACAAGCAGCCA[C/T]AATATACTGTCACCT | 996 |
rs575004401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47130864 | CCTGGGCAACAAGAG[C/T]GAAACTCCATCTCAA | 996 |
rs575090237 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178406 | TGGGCATGGTAGCAT[G/T]TGCCTGTAGTCTCAT | 996 |
rs575115224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140960 | AAACACCATACTTCA[C/T]TGTCTCCCAGTTTCC | 996 |
rs575115561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128190 | TGCACACCACCATGC[C/T]TGGCTAATTTTTGTA | 996 |
rs575199479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47182888 | CTCTCCAGCCTATCA[C/T]GGTGGTGTGAGCCTT | 996 |
rs575201520 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162563 | TAATAATTTTAAAAG[C/T]TGCATTAGTGAACTG | 996 |
rs575218423 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181311 | CAAAAACCCTGGGGG[-/A]AAAAAAAAACCTAAA | 996 |
rs575289850 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120601 | TCATCACTATTTTCC[A/G]TATCTAATGGTTCCT | 996 |
rs575366751 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47148502 | AAGACATGGACATAA[C/T]ATTTGAAGAAATAAT | 996 |
rs575367987 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138976 | GGTCATTATCTTCAC[A/G]GGATCTAAATGCTGC | 996 |
rs575384838 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190211 | AAATTCAGAGGCCTG[G/T]TTTTGAATTTTATCT | 996 |
rs575425543 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122958 | AGGTGTGAGCCACCG[C/T]GCCCAGCCTCTACAA | 996 |
rs575458787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47182103 | CTTTTAGCAGCAGTG[A/G]TTCTCAACCACTTTA | 996 |
rs575465176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47127611 | TTTCACCAAGTTGGC[C/T]GGGCTGGCCTCAAAC | 996 |
rs575723638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148064 | TTAGCAGGGCGCAGT[A/G]GCACATGCCTGTAAT | 996 |
rs575743684 | in-del | -/A | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120682 | ATTAAAGAAAAACAG[-/A]AAAGAAAGTTCCCCA | 996 |
rs575770195 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169553 | GGGAGGCTGAGGCAG[C/G]AGAATTGCTTGAACC | 996 |
rs575929900 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CDC27 | GRCh38.p7 | 17:47149091 | TCAAAAAAAAAAAAA[A/G]AAAAAGAAAAAGAAA | 996 |
rs575941416 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47152213 | TTCATCTCATTGTGA[C/T]CATCCTCCATTTATT | 996 |
rs575974340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47172907 | AATACCAGTGAGCTG[A/C]AGGATCTTCTAAGCC | 996 |
rs576090349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47145330 | CAAGGCAGAGCACCA[C/G]AGAGAAGAGAGCTAC | 996 |
rs576113765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159830 | GGCAGGGAGAAGAGA[C/T]AGATCTCCTCCAGGG | 996 |
rs576184074 | in-del | -/G/TTTTG | 0.0498607 | 0.150053 | intron-variant | CDC27 | GRCh38.p7 | 17:47134480 | GCCTAATTGTTTTTT[-/G/TTTTG]TTTTGTTTTGTTTTG | 996 |
rs576206131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47176610 | AGGGCTTTGTAAACT[A/G]TGTAAAGATTTAGGA | 996 |
rs576257036 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178293 | GTAATCCCAGCACTT[C/T]GGGAGACGGAGGTGG | 996 |
rs576299188 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165999 | GTGTATGTTCCCACA[A/T]GTGGAATTACTGGCT | 996 |
rs576311134 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134071 | ATATTAACATATTTT[C/T]AATTTTTTGTGGAGA | 996 |
rs576356174 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47167343 | CTCCAACATTCCTTA[-/T]TAAAATTTTGCCAAC | 996 |
rs576358106 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127933 | CTGGTCTCAAGTTCC[A/G]TGGACTCATGTGATC | 996 |
rs576373382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47159534 | TCACCTTGCAAGGGA[C/T]GGCGTAGGGCTTGCC | 996 |
rs576379310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47168387 | TTTCTAAGTGTATAC[A/G]AGGAAATGAGGTCAA | 996 |
rs576417957 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47155269 | ATATTTTTTTGAGAC[-/AG]AGTCTCGCTCTGTTG | 996 |
rs576419307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184995 | TCTCCCCTAAAAAAT[A/G]TTTAAGAGAAATCTG | 996 |
rs576436962 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163139 | ATTTAAGTGGTATTG[A/G]GAAGAAATAGGATAA | 996 |
rs576461681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135939 | AGGTCAGGAGATTGA[A/G]ACCATCCTGGCTAAC | 996 |
rs576487034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47129014 | TGACTCAGGTGATCC[A/G]CCCGCCTTGGTCTCC | 996 |
rs576524627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47142914 | CTCCTGACCTTAGGT[A/G]ATCTGCCTGCCTTGG | 996 |
rs576549050 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189992 | AAAAAAAGTTTAAAA[C/T]GGAGTTTGAAGGATG | 996 |
rs576558053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158714 | ACCCCTACTTCCTAC[A/G]CTAAAGCCATCCTCC | 996 |
rs576567122 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158458 | CCCATCTGCTAATCT[C/G]CAAATCAAGTGAAAG | 996 |
rs576587510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47157869 | TTGTAAGTTTCAGGC[A/G]TTTATTAATTGCATT | 996 |
rs576638495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47153923 | TCCTGTCTCTACAAA[A/G]ATAAAAGTTAAAAAA | 996 |
rs576652663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136231 | AGCAGCATTGGCAAG[G/T]TGATTGTTACATTGG | 996 |
rs576770854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47151988 | TAAAAGACAACACAA[C/T]GCTCCCATCTACATT | 996 |
rs576831797 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117837 | AGTTTTTTGTGAAAC[A/T]TAAAACTGTATCTCT | 996 |
rs576899416 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | CDC27 | GRCh38.p7 | 17:47133446 | CCAAGCTGTTTTTTT[G/T]TTTTTTTTTTGAGAC | 996 |
rs576900230 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47149574 | GGAGGAAAATGATAT[C/T]AGATCGCAATCTGGA | 996 |
rs576964439 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151865 | TACCTCTCGGCTATT[C/T]CCACTCTGTGAGAAG | 996 |
rs576978872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47126978 | TTTGTATTTTCAGTA[C/G]AGACAGGGTTTCACC | 996 |
rs576980520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138007 | GTTTTGCCATGTTGC[C/T]GAGGCTGGTCTTGGA | 996 |
rs577017520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47126228 | TTTTTCAAGTGACCA[G/T]GGAATGACACAGCCC | 996 |
rs577052923 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183079 | GAATAAAATTACTGG[A/G]TTGTTGAATATGCAT | 996 |
rs577101541 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CDC27 | GRCh38.p7 | 17:47147430 | ACAAACAAACAAACA[A/C]AAAAAAAAACACTAG | 996 |
rs577130459 | in-del | -/GAA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163579 | CATCCATATTCCTCT[-/GAA]GAAGGAGAAAAAAGA | 996 |
rs577192329 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166337 | AGGTGAGTTTTGGTA[A/G]TGTGGCTTATTAAGA | 996 |
rs577204436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158034 | TGTAATTTTCAGTTA[C/T]ATGATTCTTGAAACA | 996 |
rs577212888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47179099 | GCTGTTCCTTCTTTC[C/T]GATCCCACAGTCTCA | 996 |
rs577217193 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128081 | TGTTGCCCAGGCTGG[A/C]ATGCAGTGGCGTAAT | 996 |
rs577244449 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169646 | TGAAACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 996 |
rs577379393 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125557 | GCCTTTAAAGAAATC[-/T]TTTTTTTTTTTCCCT | 996 |
rs577404810 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47127714 | CCCTATTTTTTTTTT[G/T]TTTTTTAAGACAGGG | 996 |
rs577422321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47178674 | ATATTTTACTGTATT[C/T]AGTCCTTAAAACTAT | 996 |
rs577503859 | in-del | -/A | 0.472326 | 0.114329 | intron-variant | CDC27 | GRCh38.p7 | 17:47157396 | CACCTGTGAAGACAA[-/A]AAAAAAAAAAAGTTT | 996 |
rs577517540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47128290 | CCCACCTTGGCCTCC[C/T]GAAGAGCTGGGATTA | 996 |
rs577549999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166805 | TTTCATTCAGTTCAA[C/T]ATATTTTTAAAATCT | 996 |
rs577614716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47166264 | CATTAGGGAAGACTT[C/T]TAACTACAAATTAAA | 996 |
rs577617261 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47168252 | TGCGGGGTGGGGATG[-/A]AAAGTCCCAATCCTC | 996 |
rs577725962 | snp | A/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191118 | TGTGAGGTCCCTTAG[A/G]CCTAGGCCTGTGAGC | 996 |
rs577748308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47125503 | CTCTCACCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 996 |
rs577755584 | snp | C/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190578 | TTTCATTTTTAAAAA[C/G]AAGGCTGACAGAGCT | 996 |
rs577784847 | snp | A/G | 2.92419e-05 | 0.00382362 | intron-variant | CDC27 | GRCh38.p7 | 17:47142188 | ACTTAAAATAAGTAC[A/G]TAATAAAATACAAAG | 996 |
rs577836582 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120713 | CCCTACCCCCCATAA[A/G]TTGTCATTCATACTG | 996 |
rs577884995 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184926 | TTAAAGCCAGATGAA[C/T]GAAATGCTGCTAAAA | 996 |
rs577968384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148130 | TTGAACCCAGGAGGG[A/G]CGGAGGGTGCAGTGA | 996 |
rs578100033 | in-del | -/AA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175017 | GGAGAGAGAGAAAGA[-/AA]GAAAGAGAGAAAGAG | 996 |
rs578110101 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118870 | GGAAACTGTCCCCCA[A/G]CCAGCCATTGCCATG | 996 |
rs578157145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47173146 | GCCACATCTTTTTAA[A/G]TAGTTAACATCATTC | 996 |
rs578207037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47164536 | AAAACTGTAAACTAC[A/G]CTGGACACGGTGGCT | 996 |
rs578243462 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47164965 | AAAACTGTTTTAATA[C/T]CCCAAAGAAACCCCT | 996 |
rs745362489 | snp | C/G | 1.74931e-05 | 0.0029574 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158303 | AAGCCGATCTGTCTT[C/G]CTGTGGAGAGAAACA | 996 |
rs745395809 | snp | A/C/G | 3.33936e-05 | 0.00408606 | intron-variant | CDC27 | GRCh38.p7 | 17:47129361 | GTTTTTAAGCAATAC[A/C/G]ACACTGAAGACCCTT | 996 |
rs745396630 | snp | C/T | 1.70496e-05 | 0.00291967 | missense, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142025 | AGGCTCATCAAACCT[C/T]CTAGGAGAAAACAAC | 996 |
rs745397103 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148199 | GCGAGACTCTATCTC[-/A]AAAAAAAAAAAAAAG | 996 |
rs745399330 | in-del | -/AA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149510 | GTGAGACTCTGTCTT[-/AA]AAAAAAAAAAAAAAA | 996 |
rs745450296 | snp | A/G | 1.65051e-05 | 0.00287267 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151896 | ACAGACTTTGTTCCA[A/G]TTTGGCCGATTCTGG | 996 |
rs745491637 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158293 | ATCCTTTGGCAAGCC[A/G]ATCTGTCTTGCTGTG | 996 |
rs745504643 | in-del | -/AGA | 1.66448e-05 | 0.0028848 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189127 | CCAGCCAAGCCCCAG[-/AGA]AGAAGGTTATCATTA | 996 |
rs745558158 | in-del | -/ATATATATATAT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133107 | CACACACAAATATAC[-/ATATATATATAT]ATATATATATATATA | 996 |
rs745560502 | in-del | -/TTCT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162073 | TCTCCCCAAAATCTG[-/TTCT]TTCTCTTTCTTTCTG | 996 |
rs745682932 | snp | A/T | 3.46963e-05 | 0.00416497 | intron-variant | CDC27 | GRCh38.p7 | 17:47151973 | CTGCACTGTAAATGA[A/T]AAAAGACAACACAAC | 996 |
rs745699965 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159575 | CCCCAGTAGCCTCTG[C/T]GCACGGGGACAATCG | 996 |
rs745733863 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126734 | ACTGATTTGCAATTA[C/T]AGTACTTCAAAGAGT | 996 |
rs745773699 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183884 | AGTCTTAGCATTAAG[G/T]TTCTTTGTATTCCTA | 996 |
rs745821833 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125822 | GCTGGGATTACAGGC[A/G]TGAGCTGCTGCGCCT | 996 |
rs745856710 | snp | A/G | 6.66889e-05 | 0.00577408 | intron-variant | CDC27 | GRCh38.p7 | 17:47138704 | AGGGTGATCAAAAAG[A/G]TAACTATATAAGCAA | 996 |
rs745874758 | snp | C/T | 3.75657e-05 | 0.00433376 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120998 | TGTCATGCTGCTCTC[C/T]TGGGATTCATCTGTT | 996 |
rs745880931 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182354 | ACATTTTAAGTAACA[A/G]TAACCAAAGACATTT | 996 |
rs745914795 | snp | A/G | 0.000475577 | 0.0154131 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142307 | CTGAAATGATGGAAG[A/G]GTCCAATTTTGTAAT | 996 |
rs745939435 | snp | A/G | 1.66704e-05 | 0.00288703 | intron-variant | CDC27 | GRCh38.p7 | 17:47122436 | AAAATCATATGTATG[A/G]TACTTACTGATCTGT | 996 |
rs745969274 | snp | A/G | 0.00176067 | 0.0296181 | intron-variant | CDC27 | GRCh38.p7 | 17:47157129 | CTGTTTAATTCCTGA[A/G]ACAGAAAATTTCTAC | 996 |
rs745973141 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153988 | TAGGTACTTGGGAGG[C/G]TAAGGTGGAAGGATC | 996 |
rs746021610 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124774 | TGGAAAATTCTACTG[C/T]CCATTTGGACAGAAT | 996 |
rs746035268 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140368 | ATCCCCCTTCCTTGG[C/T]CTCCCAAAGTGCTGG | 996 |
rs746065407 | in-del | -/G | 6.96524e-05 | 0.00590096 | intron-variant | CDC27 | GRCh38.p7 | 17:47144001 | AAAAAAAATTATAAA[-/G]GAAGACATTAATATT | 996 |
rs746145910 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177760 | ATCCTCTTAGTCTCA[C/T]AGAGTTCCATAGGTA | 996 |
rs746170975 | snp | G/T | 0.000145359 | 0.008524 | intron-variant | CDC27 | GRCh38.p7 | 17:47142455 | TAAAAGGGAAGAAAT[G/T]TCACACCTGTTATAC | 996 |
rs746207522 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163193 | GTTGTGTCCTAAACA[C/T]AGAAGTCTCATGTGC | 996 |
rs746286142 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123346 | GGACTCTCAGAAGCC[A/G]TTTCTCTTAATCAAG | 996 |
rs746310606 | snp | A/G | 5.07395e-05 | 0.00503659 | intron-variant | CDC27 | GRCh38.p7 | 17:47154914 | ACAGTGAGGATCTGA[A/G]GGGCAGATTAAAAAT | 996 |
rs746352034 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130317 | GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC | 996 |
rs746397050 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147682 | CAAGATCTGCCTGGA[A/C]AACATAGCAAGACCT | 996 |
rs746492486 | snp | A/G | 6.67245e-05 | 0.00577562 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141902 | CCAATTTGGCACAGT[A/G]CCCAACCAGTATTGT | 996 |
rs746498076 | snp | A/G | 1.76758e-05 | 0.00297281 | intron-variant | CDC27 | GRCh38.p7 | 17:47123859 | GCTATGAAAGTCACT[A/G]TTTGGGACCATGACC | 996 |
rs746545405 | snp | A/G | 3.38467e-05 | 0.00411366 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138860 | ACTCTATAATTCTCA[A/G]TCCTTCTAACCTCTG | 996 |
rs746601914 | snp | A/G | 0.000148487 | 0.00861518 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157371 | AAATGTTTGGTCAGG[A/G]TCTGGCTTTTCACCT | 996 |
rs746661511 | in-del | -/CA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147426 | CAAACAAACAAACAA[-/CA]ACAAAAAAAAAAACA | 996 |
rs746699096 | snp | G/T | 1.67259e-05 | 0.00289183 | intron-variant | CDC27 | GRCh38.p7 | 17:47129346 | ACAAGGGATAACGTT[G/T]TTTTTAAGCAATACA | 996 |
rs746727383 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187578 | AAGTGCTGGGATTTC[A/C]GGTGTAAGCCACCAC | 996 |
rs746798199 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151870 | CTCGGCTATTTCCAC[C/T]CTGTGAGAAGACAGA | 996 |
rs746811966 | snp | C/T | 1.95915e-05 | 0.00312976 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143971 | GTGGGGCTCAATACC[C/T]GAGGTGTTGTACTAA | 996 |
rs746915890 | in-del | -/A/GGCG | 0.000275541 | 0.0117347 | intron-variant | CDC27 | GRCh38.p7 | 17:47137363 | AGCACACCAGGCCTT[-/A/GGCG]AAAAAAATGGGAACA | 996 |
rs746933505 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180744 | AGATGGCTGTGCTAA[G/T]GGCTTTAAATAAACC | 996 |
rs746939142 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123779 | CAGTTCGGAGCTTTA[G/T]TTTAATTTGCTCAAT | 996 |
rs746941225 | snp | C/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142238 | ACAGACCTGCTGCTG[C/T]TTTTTGTAGATTAAA | 996 |
rs746951515 | in-del | -/CA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164853 | AACTGTAAACTAAAC[-/CA]CAGAGCTTATTTGAA | 996 |
rs747002160 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126768 | TAAAAGTTGAAACGG[A/G]CTTATTAGATTTAAA | 996 |
rs747099686 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189209 | TCTGCAGTGCCTCAG[G/T]CCCCCCCTGTAGCGG | 996 |
rs747115024 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176609 | CAGGGCTTTGTAAAC[G/T]GTGTAAAGATTTAGG | 996 |
rs747125863 | in-del | -/GCCGATTCTGGC | 1.65154e-05 | 0.00287358 | cds-indel, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151901 | CTTTGTTCCAGTTTG[-/GCCGATTCTGGC]AACAGACTGTAAAAC | 996 |
rs747163950 | snp | A/C | 1.75203e-05 | 0.00295971 | intron-variant | CDC27 | GRCh38.p7 | 17:47142060 | TAAACAAAGGAAAAA[A/C]CGCAATAAACTAGTC | 996 |
rs747188366 | snp | A/C/G | 0.00618833 | 0.0552816 | intron-variant | CDC27 | GRCh38.p7 | 17:47157127 | ATCTGTTTAATTCCT[A/C/G]AAACAGAAAATTTCT | 996 |
rs747327103 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177490 | GCTGATGCAGGAGAA[C/T]TGCCTGAACCTGGGA | 996 |
rs747349709 | snp | A/G | 0.000478252 | 0.0154563 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132299 | ACTTTGAGGGTTGAT[A/G]TCAAGCGCTTTTTGG | 996 |
rs747358702 | snp | A/G | 0.00163862 | 0.0285767 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169988 | AACAATATCATCATG[A/G]CTTTTCTGCTTATTA | 996 |
rs747403186 | snp | C/T | 0.000161084 | 0.00897307 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142288 | ATTGTGGATATTTTC[C/T]CTTCTGAAATGATGG | 996 |
rs747418004 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138643 | AGAAATAAGCGTGGG[C/T]GACACTAAATAGTGT | 996 |
rs747450241 | snp | G/T | 0.00333976 | 0.0407275 | stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171955 | TGCAAGCAGGTATTT[G/T]CATTGCGGTGTAGTA | 996 |
rs747517102 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174533 | TAATATATTGCATAA[C/T]CATGAATGAAGTTAG | 996 |
rs747578619 | snp | C/T | 4.3368e-05 | 0.0046564 | intron-variant | CDC27 | GRCh38.p7 | 17:47137106 | AAAATTAGTAAGTAC[C/T]AGCACCATCAATACG | 996 |
rs747618797 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144906 | ACATAAATCCTTTTA[A/G]TCTGCATCTGATAAA | 996 |
rs747637001 | snp | G/T | 2.29056e-05 | 0.00338412 | intron-variant | CDC27 | GRCh38.p7 | 17:47154890 | GAGAATGGCAAATCA[G/T]TCTTAGGGACAGTGA | 996 |
rs747660864 | snp | C/T | 1.66377e-05 | 0.00288419 | intron-variant | CDC27 | GRCh38.p7 | 17:47138722 | ACTATATAAGCAAAG[C/T]ATTTTGGTTAACATA | 996 |
rs747677921 | snp | A/G | 0.00252064 | 0.0354114 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154718 | TCAATTACAGGAGGT[A/G]TATTAGTGTAGTTTT | 996 |
rs747692749 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179366 | CAAGAATTCTGAGGT[C/T]GGTTCAGTGGGAATG | 996 |
rs747730720 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134874 | AAGTAATCTTCCAGC[C/T]TCAGCTTCCTAAAGT | 996 |
rs747732712 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180946 | ACAGACTCTTTTCTT[-/A]AAAAAAAAAAAAAAA | 996 |
rs747753741 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147025 | CTATAATCACACCAC[C/T]GTACTCTAGCCTGGG | 996 |
rs747794089 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128325 | TGTGAGCCACTGCGC[C/T]CAGCCCTGAATTTAT | 996 |
rs747825154 | snp | C/T | 3.35582e-05 | 0.00409609 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138843 | AGATCTCCATGCCTT[C/T]AACTCTATAATTCTC | 996 |
rs747852462 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145864 | ATCGTGCCATTGCAT[C/T]GCAGCCTGGGCGACA | 996 |
rs747886074 | in-del | -/T | 1.77722e-05 | 0.00298091 | intron-variant | CDC27 | GRCh38.p7 | 17:47151980 | TAAATGATAAAAGAC[-/T]AACACAACGCTCCCA | 996 |
rs747901912 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184342 | AATTCAATAAATATG[G/T]AGTTTCTGTTGCATA | 996 |
rs747905668 | snp | G/T | 3.30087e-05 | 0.00406242 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122467 | TCTTCTTGGGTTATT[G/T]GCTCCTCATCATCTG | 996 |
rs747913020 | snp | C/T | 4.89896e-05 | 0.00494898 | intron-variant | CDC27 | GRCh38.p7 | 17:47122667 | ATAAAATTCTAACTA[C/T]ATATATACTTATTTA | 996 |
rs747953129 | snp | C/T | 0.0212898 | 0.100954 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157359 | AGATGTGAATTTAAA[C/T]GTTTGGTCAGGATCT | 996 |
rs748085844 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155434 | TAATTTTAGTAGAGA[G/T]AGGGTTTCACCATGT | 996 |
rs748101806 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47154172 | TTCATTTTCATGTTA[A/C]AACTATACATCCATG | 996 |
rs748104586 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139166 | TCTACCAAAAAGACC[A/G]AAGAGAAATCTATAC | 996 |
rs748124066 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182279 | TTTAATTTTTTGAAT[A/G]TATGTTTTCTCTTTT | 996 |
rs748148225 | snp | C/G | 1.77149e-05 | 0.0029761 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143959 | GGAGATGTAATAGTG[C/G]GGCTCAATACCTGAG | 996 |
rs748157932 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159957 | CCCGGCCCCATCCAC[A/G]GCTGCGACCCCAGCC | 996 |
rs748165922 | in-del | -/A/AC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147427 | AAACAAACAAACAAA[-/A/AC]CAAAAAAAAAAACAC | 996 |
rs748198995 | snp | C/T | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137254 | TGCCCTAATAGAGTA[C/T]AGGCATAAGCGTAAT | 996 |
rs748199763 | snp | C/T | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117201 | GCTTTTAAACAAAGT[C/T]TGCACTTACAAAGAA | 996 |
rs748201552 | snp | C/G | 1.64895e-05 | 0.00287132 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151853 | AAGAATTGGAGTTAC[C/G]TCTCGGCTATTTCCA | 996 |
rs748312745 | snp | G/T | 4.97558e-05 | 0.00498753 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156974 | GACCAGTTTTTGGTT[G/T]ATTTTGAACCTGTTT | 996 |
rs748409583 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176005 | CATTTTTTTTTCATC[C/G]GGTAAGGACTATGAT | 996 |
rs748410715 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126353 | TCATAATTCAGCGAA[A/G]CCCCAAGCTCATACC | 996 |
rs748463562 | snp | C/T | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191287 | GGAAACAATCTACCA[C/T]GCTAGATATGAGATG | 996 |
rs748538860 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119858 | TAAATGTTTTGGTGA[C/T]TCACACTACTGAAAA | 996 |
rs748545575 | snp | A/T | 8.30958e-05 | 0.00644523 | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157053 | TACAGCTGAATCAAT[A/T]TAAGACACTGAGGAA | 996 |
rs748549039 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162695 | TGATCCTTTGTGCTG[-/A]AAAGTCTCATTTCCA | 996 |
rs748553753 | in-del | -/TTTAG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123775 | CACTCAGTTCGGAGC[-/TTTAG]TTTAATTTGCTCAAT | 996 |
rs748554822 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47152675 | TGTTACCCTGATGTC[C/T]TGTACACAATCCTCA | 996 |
rs748643428 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177303 | AAATAAAGACCGGAT[A/G]CAGTGGCTCCCGCCT | 996 |
rs748723120 | snp | C/T | 1.90376e-05 | 0.0030852 | intron-variant | CDC27 | GRCh38.p7 | 17:47171907 | AGCTAGAAAATATTT[C/T]AAAACTTACTTGCTG | 996 |
rs748733469 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129960 | TTCATCAGGTTTATG[C/T]GGTCTTTCAAATATT | 996 |
rs748755064 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158474 | CAAATCAAGTGAAAG[C/T]GCACAGAACATGAAT | 996 |
rs748773303 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134867 | TGGTCTCAAGTAATC[C/T]TCCAGCTTCAGCTTC | 996 |
rs748791542 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175175 | AAGGTCTTTTGAGTG[A/T]AAGTCCAAAATAATT | 996 |
rs748832141 | snp | C/T | 3.29908e-05 | 0.00406132 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132294 | ACTGAACTTTGAGGG[C/T]TGATATCAAGCGCTT | 996 |
rs748858516 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118098 | ACACACACTTCATAC[C/T]CACACTTGCATTTTC | 996 |
rs748858854 | snp | C/T | 0.000479382 | 0.0154745 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169962 | AAGCAAGCTGAATCA[C/T]CAAACTCAGTAACAA | 996 |
rs748983028 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119795 | TCATAAGAATGTTTT[C/T]TCCCCCAAGCTAAAA | 996 |
rs749000797 | in-del | -/ATC | 1.64855e-05 | 0.00287097 | cds-indel, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169979 | AAACTCAGTAACAAT[-/ATC]ATCATGGCTTTTCTG | 996 |
rs749008637 | in-del | -/AT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163203 | AAACATAGAAGTCTC[-/AT]GTGCTGTAATAGACA | 996 |
rs749015475 | snp | C/T | 0.000155773 | 0.00882395 | stop-gained, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137355 | GTTCCCTGCAGCACA[C/T]CAGGCCTTAAAAAAA | 996 |
rs749048626 | snp | C/G | 1.65699e-05 | 0.00287831 | missense, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122448 | ATGATACTTACTGAT[C/G]TGTTCTTCTTGGGTT | 996 |
rs749083538 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126990 | GTAGAGACAGGGTTT[C/T]ACCATGTTGGCCAGG | 996 |
rs749097395 | in-del | -/A | 1.70545e-05 | 0.0029201 | splice-donor-variant | CDC27 | GRCh38.p7 | 17:47157228 | GAATATAAGACACTT[-/A]CAATTGTGTCCTGGG | 996 |
rs749104819 | snp | A/G | 1.66585e-05 | 0.00288599 | intron-variant | CDC27 | GRCh38.p7 | 17:47138716 | AAGGTAACTATATAA[A/G]CAAAGTATTTTGGTT | 996 |
rs749243155 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185353 | CCGGCTAATTTTTTT[C/T]GTATTTTTAGTAGAG | 996 |
rs749245112 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168135 | TTTACGGAGGCTTCA[C/T]TACATAGGCATTACT | 996 |
rs749272220 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128291 | CCACCTTGGCCTCCC[A/G]AAGAGCTGGGATTAC | 996 |
rs749275368 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187078 | TGGCTTCTTATACTA[A/T]ACAACCAAAATTTTC | 996 |
rs749283766 | snp | C/T | 1.74866e-05 | 0.00295686 | intron-variant | CDC27 | GRCh38.p7 | 17:47122625 | AACAGCAGCACTACA[C/T]TTTTCATTAAGTTGT | 996 |
rs749330612 | snp | G/T | 1.70336e-05 | 0.00291831 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143942 | GAGGCAGTGCGTTTG[G/T]GGGAGATGTAATAGT | 996 |
rs749384405 | in-del | -/TG | | | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117844 | TGTGAAACATAAAAC[-/TG]TATCTCTGTTTTTCT | 996 |
rs749389222 | snp | A/G | 5.39437e-05 | 0.00519316 | intron-variant | CDC27 | GRCh38.p7 | 17:47143837 | AACAGAAATGTTAGC[A/G]GGCGAAGCATTAAGT | 996 |
rs749389340 | snp | A/G | 3.29598e-05 | 0.00405941 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157342 | TTGCTAAAGTTCTGT[A/G]AAGATGTGAATTTAA | 996 |
rs749443481 | in-del | -/CCCC | 1.76799e-05 | 0.00297315 | intron-variant | CDC27 | GRCh38.p7 | 17:47122627 | AGCAGCACTACATTT[-/CCCC]TTCATTAAGTTGTGA | 996 |
rs749498431 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123614 | GTCAGGTTTCACCAT[C/G]TTGGTCAGGCTGGTC | 996 |
rs749515122 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169563 | GGCAGGAGAATTGCT[A/T]GAACCCTGGAGGTGG | 996 |
rs749517914 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180660 | AGCATCTTAGAAAGG[C/G]AATTATAATAATGAC | 996 |
rs749590645 | snp | G/T | 1.65864e-05 | 0.00287974 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156957 | TCCTCCTAATAAACT[G/T]CGACCAGTTTTTGGT | 996 |
rs749641683 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127420 | TTTACGTTTTTTTTT[G/T]AGATGGAGTTTCACT | 996 |
rs749696533 | snp | C/T | 3.49644e-05 | 0.00418103 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181581 | TGCATAAAGGCGTTC[C/T]GCGAGGAAAACCGCA | 996 |
rs749697332 | snp | A/G | 2.14945e-05 | 0.00327823 | intron-variant | CDC27 | GRCh38.p7 | 17:47156866 | TATGAGTTATCATAA[A/G]ATCATTTGGTATTAT | 996 |
rs749723942 | in-del | -/TAAAAAA | 0.00754326 | 0.0609486 | intron-variant | CDC27 | GRCh38.p7 | 17:47137363 | CAGCACACCAGGCCT[-/TAAAAAA]ATGGGAACAAAAACC | 996 |
rs749737807 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174234 | TACCCCAAACACAAC[C/T]AAAGAAGCAGTGGTA | 996 |
rs749772634 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150954 | GGAGAATCACTTGAA[C/T]CCGGGAGGCGGAGGT | 996 |
rs749781258 | snp | G/T | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191000 | GGGTCCTTCATTTCT[G/T]CTCTGCATGACCTCT | 996 |
rs749826511 | snp | C/T | 1.65754e-05 | 0.00287879 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141940 | AGAAGGTAGATGGCT[C/T]AAAATATTTATAGCT | 996 |
rs749857065 | snp | A/G | 2.08422e-05 | 0.00322811 | intron-variant | CDC27 | GRCh38.p7 | 17:47142222 | ATATTAAGCATTTAA[A/G]ACAGACCTGCTGCTG | 996 |
rs749867179 | in-del | -/TCTGGCAGATT/TCTGGCAGATTT/TCTGGCAGATTTTTATCCAAGTCTG/TCTGGCAGATTTTTATCCACGTCTG/TCTGGCGAATTT/TCTGGCGAATTTTTATCCATGTCTG | 0.00427779 | 0.0460945 | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47137361 | GCAGCACACCAGGCC[lengthTooLong]TTAAAAAAATGGGAA | 996 |
rs749912253 | snp | A/C | 1.73851e-05 | 0.00294826 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157112 | AAGATTCTAAATTCA[A/C]TCTGTTTAATTCCTG | 996 |
rs749947961 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122284 | CATTATCTGACTTTA[C/T]ATGCATTTTGTTATT | 996 |
rs749951168 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167211 | TTTGAGATTTTCTTA[C/T]CCATGTGTGACTTTT | 996 |
rs750065794 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175094 | AAGGAAGGAAGGAAG[G/T]AAGTAAGTTGTAGCA | 996 |
rs750121183 | snp | A/C/T | 4.95081e-05 | 0.00497514 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132281 | GTGGCAAAGTAAAAC[A/C/T]GAACTTTGAGGGTTG | 996 |
rs750129780 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134622 | CTGGGACTACAGGCA[C/T]GCATCACCACACCCA | 996 |
rs750151095 | snp | C/T | 2.06031e-05 | 0.00320953 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47172004 | AGTCTATATGCTTTA[C/T]ATGCCTTTCCTGAGC | 996 |
rs750217725 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144602 | TAGAGCGAAAGGAGC[C/T]TCTGTACATTTTTAC | 996 |
rs750259404 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145578 | AGTAACTCCTAGATA[C/T]TTTCTGGATGGGTGC | 996 |
rs750259810 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176640 | AACAGATCCTTACAA[A/C]AATTAGATACTTCTG | 996 |
rs750279680 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131206 | CAACTTCACCAAAAG[A/G]TGTCAAGAGATTTAA | 996 |
rs750294711 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162168 | ATAGCACTGACTCCT[C/T]CTTCTTCTCCTCTGA | 996 |
rs750384535 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160526 | CCACAGCACCTGGTC[A/G]CCTCCTCCTTAGCTT | 996 |
rs750439374 | in-del | -/C | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158275 | TCTTTTGGTAACATT[-/C]TGATCCTTTGGCAAG | 996 |
rs750440330 | snp | C/T | 5.49164e-05 | 0.00523977 | intron-variant | CDC27 | GRCh38.p7 | 17:47154829 | AAAAAGTCATCAAGG[C/T]ATATATAAAGCAGCA | 996 |
rs750466800 | snp | C/T | 1.66443e-05 | 0.00288477 | synonymous-codon, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122589 | GTGCGTTTGACCTAA[C/T]TTCTTGTAAACCTAA | 996 |
rs750487606 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188287 | AAGGCACAAAAGATA[C/G]AGTTTCTCCAGATGT | 996 |
rs750572949 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171577 | CACCTAAACACAAGG[C/G]AGCCTTAATCTCAAG | 996 |
rs750606463 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156688 | CCTGACCTCAGGTGA[A/T]CTGCCTGCCTTGGCC | 996 |
rs750648328 | snp | A/G | 1.68866e-05 | 0.00290569 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47123896 | TTTACCTTTCCTATT[A/G]AGAAGTAAACGAGGG | 996 |
rs750680515 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155277 | TTGAGACAGAGTCTC[A/G]CTCTGTTGCCCAGGC | 996 |
rs750687478 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173429 | AAACTATTAATTTTA[C/T]TGAGCTACAACTTCT | 996 |
rs750708395 | snp | C/G | 3.29614e-05 | 0.00405951 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157335 | CAGACAGTTGCTAAA[C/G]TTCTGTAAAGATGTG | 996 |
rs750711189 | in-del | -/ACCT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140449 | GTAACAAGATAAAAG[-/ACCT]ACCAGCCAAATATAG | 996 |
rs750756240 | snp | A/C/T | 3.38096e-05 | 0.00411143 | intron-variant | CDC27 | GRCh38.p7 | 17:47151779 | GTTTTATGCCAAGAA[A/C/T]AGTTGAATAATTACA | 996 |
rs750796318 | snp | C/T | 0.000138648 | 0.00832495 | intron-variant | CDC27 | GRCh38.p7 | 17:47157417 | AAAAAAGTTTGTCTC[C/T]GAGGAAGTGAGGAAT | 996 |
rs750875468 | in-del | -/AGTTGTTT/AGTTGTTTCCGTAAGAAAGGT/AGTTGTTTCCGTAAGAAAGGTCT/AGTTGTTTCCGTAAGAAAGGTCTCAGG | | | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47157124 | CAATCTGTTTAATTC[lengthTooLong]CTGAAACAGAAAATT | 996 |
rs750878717 | snp | C/T | 1.77206e-05 | 0.00297657 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181570 | TTCAAACCTTCTGCA[C/T]AAAGGCGTTCTGCGA | 996 |
rs750937137 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166073 | TTTTATATATCACTG[A/G]TACATCTGATTTCCT | 996 |
rs750988492 | snp | C/T | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137213 | AAGCTAATGCTTTGT[C/T]CAATTCTTCAGTTAA | 996 |
rs751045019 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145881 | CAGCCTGGGCGACAA[C/G]AGCGAAACTCTGTCT | 996 |
rs751153343 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150349 | TTTTTGCAGATGTCA[C/T]TGAGTTAAGCTGAGG | 996 |
rs751160152 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181665 | GAAAAAGAACATAAA[C/T]ATACATACATACAGA | 996 |
rs751208949 | in-del | -/AA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178555 | TAAATAAAAATAAGA[-/AA]AAAAAAAAAAAACCC | 996 |
rs751220775 | in-del | -/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189475 | CTGACCCAAAGCGTA[-/G]GTTTCTCTTCTCAGC | 996 |
rs751263845 | snp | C/T | 3.34052e-05 | 0.00408674 | intron-variant | CDC27 | GRCh38.p7 | 17:47132240 | AATAGAGTATTAATG[C/T]TTAGAAAGCTACTTA | 996 |
rs751273226 | snp | A/G | 0.000727525 | 0.0190587 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142005 | CTTTCCCCATTTCAC[A/G]AAGAAGGCTCATCAA | 996 |
rs751280080 | snp | G/T | 0.00387576 | 0.0438504 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157095 | GGAGTACTTTGAATT[G/T]GAAGATTCTAAATTC | 996 |
rs751280585 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136361 | AAAATGTTTTAGTAA[C/T]ATAATGCTTCAGATT | 996 |
rs751324279 | snp | C/T | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117632 | AGAATAAGCAGTTGA[C/T]TTGCAAATTCGCAGC | 996 |
rs751375797 | snp | A/G | 1.65405e-05 | 0.00287576 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129509 | TCTCTGATTTTTTCA[A/G]TGCATGTTGAACCTG | 996 |
rs751420012 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168911 | AGTCACTTCTCCCAC[A/G]GGGGAGAAGTGACAA | 996 |
rs751424835 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134467 | GCATACACCACCATG[A/C]CTAATTGTTTTTTTT | 996 |
rs751443752 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159484 | TGCTCCTGGGGGTGC[A/G]ACGAGGCGCACCAGC | 996 |
rs751455168 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126285 | TTAACTTTTCCTTAT[A/G]CCCTTTTCATACAGT | 996 |
rs751468615 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174931 | ACTGCACTCCAGCCT[A/G]GGCAACAGCGAAACT | 996 |
rs751521868 | snp | A/C | 1.71749e-05 | 0.00293038 | intron-variant | CDC27 | GRCh38.p7 | 17:47151963 | GAATTATGGGCTGCA[A/C]TGTAAATGATAAAAG | 996 |
rs751556261 | snp | A/G | 2.61777e-05 | 0.00361775 | intron-variant | CDC27 | GRCh38.p7 | 17:47154790 | AAAATCCCAAAACTG[A/G]GAAGAGGTTGAAATC | 996 |
rs751618488 | snp | A/C | 1.71784e-05 | 0.00293069 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47170039 | TTGTTCCCCTTCTGC[A/C]AGCCTTTAAAATACA | 996 |
rs751625885 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129337 | TTATTGAAAACAAGG[G/T]ATAACGTTGTTTTTA | 996 |
rs751647028 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128133 | CCTCCTGGGTTCAAG[G/T]GATTCTCGTGCCTCA | 996 |
rs751676877 | snp | A/G | 3.40217e-05 | 0.00412428 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154690 | TTTTGAAGGGGCTCC[A/G]GTGGATGGCACATCA | 996 |
rs751718000 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146469 | ACCCAAAGCTGGGGA[A/G]AGTATTACTGAAAAG | 996 |
rs751728749 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171370 | CAAATATCTAACACC[A/G]TTTACACATGTGACC | 996 |
rs751772660 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153777 | CCATATACCTATAAA[A/C]GGGAACATTATAAAA | 996 |
rs751777383 | snp | A/G | 1.65982e-05 | 0.00288077 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138791 | GACAGAACTGAAAGA[A/G]CAACATCTTTTTGAA | 996 |
rs751779345 | in-del | -/G/T | 3.38979e-05 | 0.0041168 | intron-variant | CDC27 | GRCh38.p7 | 17:47157399 | CTGTGAAGACAAAAA[-/G/T]AAAAAAAAGTTTGTC | 996 |
rs751822281 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169356 | CAAGGTAAAATAAAC[G/T]AACATGGGGCCGGGT | 996 |
rs751829755 | snp | A/G | 0.000184652 | 0.00960687 | intron-variant | CDC27 | GRCh38.p7 | 17:47122424 | TTCTAAATACTCAAA[A/G]TCATATGTATGATAC | 996 |
rs751916971 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155197 | ATGGTCATGCTATTT[G/T]AGTAGTTCCCCGGCC | 996 |
rs751924279 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157322 | TGCAAGAGTTGGGCA[C/G]ACAGTTGCTAAAGTT | 996 |
rs751941268 | snp | A/G | 1.7093e-05 | 0.00292339 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142403 | TGTTTGGGATTTTAG[A/G]TGGAAACTTCATTTT | 996 |
rs752005511 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141122 | TCTAGAAGAGAGTCC[A/G]GGATATCATATGCAC | 996 |
rs752042429 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123118 | TATTTTCAGAATTCC[C/T]TGCTTCTATCTTTCA | 996 |
rs752102389 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180204 | TTTAAATAGATTATT[C/T]ACAATAAACATCACT | 996 |
rs752115627 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122927 | ATCCACCTGCCTCCC[A/T]AAGTGCTGGGATTAC | 996 |
rs752138213 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156476 | TTTTTGAGTTGGAGT[C/T]TTGGTCTGTCGCCCA | 996 |
rs752174026 | snp | A/G | 1.69243e-05 | 0.00290893 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143933 | AACTTCTTCGAGGCA[A/G]TGCGTTTGGGGGAGA | 996 |
rs752181878 | snp | A/G | 1.85115e-05 | 0.00304227 | intron-variant | CDC27 | GRCh38.p7 | 17:47181551 | TCTACAGCAATGAAT[A/G]GATTTCAAACCTTCT | 996 |
rs752206295 | in-del | -/A | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190567 | GATATTTTTTCTTTC[-/A]TTTTTAAAAACAAGG | 996 |
rs752303348 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162350 | CTTCAATTCATCTAT[C/T]TAGGCCCCTTCTGTC | 996 |
rs752312021 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121070 | GACAAATATGTCCTG[C/T]TGGTTCATGAAAACA | 996 |
rs752356743 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168305 | TGCCAGTCCCCATCC[C/T]GAAGCTACCTAGGGG | 996 |
rs752385911 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164149 | TGTTATAACTGCCTA[C/T]AGTATTCAGTAAGGT | 996 |
rs752413044 | snp | A/G | 1.78691e-05 | 0.00298902 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156919 | TTGACTTACCTTGGG[A/G]TTAATGGACTAAGAG | 996 |
rs752416702 | snp | C/T | 1.67036e-05 | 0.0028899 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189100 | TACGCTGCTGCTTCC[C/T]GACCGAGGCTGCCAG | 996 |
rs752506620 | snp | G/T | 0.00478245 | 0.0486657 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157020 | TCCTGTTCCCAGTGG[G/T]ACAGTATCAGGTGAA | 996 |
rs752511741 | snp | A/T | 1.69183e-05 | 0.00290841 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158225 | TTCACATAATGATTC[A/T]AAGGGAGACCAGAGG | 996 |
rs752553427 | snp | C/G | 0.000185803 | 0.00963675 | stop-gained, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141866 | ACTTGCATGTACTCT[C/G]AAAGTTCAAAATAGG | 996 |
rs752581323 | snp | A/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47188916 | ACGGGAAAGGCGGTT[A/C]TTTTCGCCGAAGCCG | 996 |
rs752603952 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150028 | GAAACCACAACCACA[A/G]TAATGCACTGTGGGG | 996 |
rs752626597 | snp | A/G | 1.64936e-05 | 0.00287168 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129479 | CAATGGCTTTGTTTA[A/G]GGTATCCAAAGCCTT | 996 |
rs752675992 | snp | G/T | 3.36129e-05 | 0.00409943 | intron-variant | CDC27 | GRCh38.p7 | 17:47132219 | ACATATTTCAAAAGG[G/T]AGATTAATAGAGTAT | 996 |
rs752792423 | snp | C/G | 1.68995e-05 | 0.00290679 | intron-variant | CDC27 | GRCh38.p7 | 17:47151946 | AAAAGTCTAAGGTTT[C/G]TGAATTATGGGCTGC | 996 |
rs752795044 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178128 | TCCAAAACAGCAAAT[A/C]TCAACTCACTAGTGG | 996 |
rs752845490 | snp | C/T | 1.71009e-05 | 0.00292406 | intron-variant | CDC27 | GRCh38.p7 | 17:47169889 | GTATGGAAATGCTTT[C/T]CTGACAGTTTGAATC | 996 |
rs752874259 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160125 | GTTTCTTTCTAAATC[A/G]GGTGTATAAACGCTT | 996 |
rs752901078 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167715 | ATGTCTGGGTTTTCT[A/G]ATTCCCCCTAAACAC | 996 |
rs752920690 | snp | G/T | 0.0002596 | 0.01139 | intron-variant | CDC27 | GRCh38.p7 | 17:47154663 | AACTGCATTTTACAT[G/T]GAAAATACCTTTTTT | 996 |
rs752964314 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183615 | CCATTATTATACACT[C/T]TAATTGCACCAAGTA | 996 |
rs752977065 | snp | A/C | 1.66244e-05 | 0.00288304 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137328 | ATCATGTTCCCGTTG[A/C]AGACTGAAACAGTTC | 996 |
rs752996101 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145455 | ATTTGTCTGGTCCAC[A/G]TCCCAGGCTCCTGAG | 996 |
rs753013739 | snp | C/T | 1.68718e-05 | 0.00290441 | intron-variant | CDC27 | GRCh38.p7 | 17:47122412 | CAAAAGGTAACTTTC[C/T]AAATACTCAAAATCA | 996 |
rs753067072 | snp | A/C | 1.89647e-05 | 0.00307929 | stop-gained, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120943 | CCAGAAGTTAAAATT[A/C]ATCACTTTCAGCTGC | 996 |
rs753092125 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132088 | GGGATAAGGGCAATT[A/C]TGTGATTTTTTATGC | 996 |
rs753097423 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169271 | GTTGAGATTACAGGC[A/G]TGAGACAATGCACCT | 996 |
rs753145126 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161062 | TCAAAAATTTCTTTC[-/T]TTTTTTTTTTTTTAA | 996 |
rs753175587 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128939 | ACCATGCCCAGCTAA[C/T]TTTTTGTATTTTTAG | 996 |
rs753186804 | snp | A/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189030 | GCAGGACACGGCAGC[A/T]GGGGAGGCGGGAGAA | 996 |
rs753230227 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153648 | GCTTCCATTTCTTGA[A/G]TATTTATGAAGCATG | 996 |
rs753283403 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122149 | ATTTAAAAAACTACA[-/T]TTTTTATGAAGCAGA | 996 |
rs753311573 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159027 | AAAATGCTGGAATTA[-/C]AGGCGTGATCCACCA | 996 |
rs753324329 | snp | C/T | 1.68738e-05 | 0.00290458 | intron-variant | CDC27 | GRCh38.p7 | 17:47157203 | AGTTTTCATAATATT[C/T]TGAACACTAGAATAT | 996 |
rs753339972 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153573 | ACTATAAGAAGAAAC[A/T]TGTTTCTATTAAGGT | 996 |
rs753359220 | snp | C/T | 1.73126e-05 | 0.00294211 | intron-variant | CDC27 | GRCh38.p7 | 17:47143874 | GACATACAGAAATCT[C/T]TAAATTACCTTGGTT | 996 |
rs753447906 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176907 | ATCTTAACACAATCT[A/G]GTAAATAAGTTTTTT | 996 |
rs753535732 | snp | A/T | 1.91507e-05 | 0.00309434 | intron-variant | CDC27 | GRCh38.p7 | 17:47156907 | AAAGTATCTTGTTTG[A/T]CTTACCTTGGGGTTA | 996 |
rs753579922 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138366 | AATCTTACAAGATTA[C/G]AGCATGTACATTAAT | 996 |
rs753643520 | snp | A/G | 0.000316537 | 0.0125765 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138823 | ATGCCAAAGTGTTGT[A/G]GAGTAGATCTCCATG | 996 |
rs753645475 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148896 | CTAGCCTGGCCAACA[C/T]GGTGAAAGCCAATCT | 996 |
rs753652013 | in-del | -/AT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175513 | TATGATTTGTGACAC[-/AT]GTTTCAAATTGATTA | 996 |
rs753652128 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129556 | TGTTAATACTCCCTC[C/T]TGATATTTATGAAGA | 996 |
rs753652718 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119594 | AAAATGTTAACAACT[A/T]AAATTTCTCTAAAAA | 996 |
rs753732656 | in-del | -/T | 0.00110792 | 0.0235102 | intron-variant | CDC27 | GRCh38.p7 | 17:47137130 | CAATACGACTTTGTC[-/T]TTGTACTTCATTACC | 996 |
rs753752876 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169664 | AAAAAAAAAAAAAAA[-/T]AGAAACAAACAAAAA | 996 |
rs753814579 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187013 | CATTGATCTTTATCA[C/T]TGTAGCCAAAGTTGC | 996 |
rs753869605 | in-del | -/GAT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135414 | CCATAACTAGATGAT[-/GAT]GATGATGATGATGAT | 996 |
rs753873558 | snp | C/T | 1.70064e-05 | 0.00291597 | intron-variant | CDC27 | GRCh38.p7 | 17:47141850 | ACCATTTTCTATACT[C/T]ACTTGCATGTACTCT | 996 |
rs753878999 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177836 | ATTTTCTGAACATAA[C/G]TCTTATTTTATATGT | 996 |
rs753882483 | snp | A/C | 7.09585e-05 | 0.00595602 | intron-variant | CDC27 | GRCh38.p7 | 17:47158179 | AGGAGATGGGAACCC[A/C]CCCACCTCTCAACCC | 996 |
rs753924753 | snp | A/G | 1.65031e-05 | 0.00287251 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129423 | TGCAAATAAAACTGA[A/G]GCTCTGTGAAATTTG | 996 |
rs753974642 | snp | A/G | 1.68471e-05 | 0.00290228 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47123907 | TATTAAGAAGTAAAC[A/G]AGGGATTCTTTGGGA | 996 |
rs753983296 | snp | A/C | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117384 | GGAACTGCCCAGCTC[A/C]CCCCACCTTCACATG | 996 |
rs753989096 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174885 | CACTTAAACCCGGGA[A/G]GCAGTGGTTGCAGTG | 996 |
rs754036649 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182156 | TTAAAATGTATGTCA[C/T]CCTCCCACAAAAACT | 996 |
rs754046342 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158765 | CTGAGACTATAGGTG[C/T]GCACCACCATATCCG | 996 |
rs754050732 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143555 | CAATTCTTTTGTGCC[A/G]TGATTTAATAGTAAC | 996 |
rs754105922 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120708 | CCCCACCCTACCCCC[C/T]ATAAATTGTCATTCA | 996 |
rs754116553 | snp | A/G | 5.01266e-05 | 0.00500607 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151809 | AATGATAAATACCTT[A/G]TTTGTGGACCAGAAC | 996 |
rs754116627 | snp | C/T | 6.42213e-05 | 0.00566626 | intron-variant | CDC27 | GRCh38.p7 | 17:47158351 | ACAAACCCCAAAACC[C/T]GTATCATAAACTTTT | 996 |
rs754161329 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183329 | GATTAATATGCCTTA[C/G]ATACAGTAAAGGCTC | 996 |
rs754213786 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126311 | ACAGTCACATTTCTA[C/T]ATCTAATCCATGCAG | 996 |
rs754230179 | snp | A/G | 1.66358e-05 | 0.00288402 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189135 | GCCCCAGAGAAGAAG[A/G]TTATCATTACCTGGA | 996 |
rs754232623 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155208 | ATTTTAGTAGTTCCC[C/T]GGCCTCAGGACCTGA | 996 |
rs754301319 | snp | C/T | 0.000101533 | 0.00712434 | intron-variant | CDC27 | GRCh38.p7 | 17:47122395 | GCCTACAAATCCTTA[C/T]GCAAAAGGTAACTTT | 996 |
rs754306390 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143888 | TTTAAATTACCTTGG[C/T]TGTGGAGCTGTCACT | 996 |
rs754380874 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167517 | CTAGTTATCACAACC[C/T]CTCTTCTTAACCAGG | 996 |
rs754405109 | snp | A/G | 2.05139e-05 | 0.00320258 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120917 | CACATCCAGTTGTAA[A/G]AGTCTGATTTCCAGA | 996 |
rs754431622 | snp | A/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157041 | ATCAGGTGAAATTAC[A/T]GCTGAATCAATATAA | 996 |
rs754437495 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180609 | CCAAGGAAATGACTC[-/A]AAAAAAAAAAAAAGC | 996 |
rs754480874 | in-del | -/AAATAA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178541 | CAAAAATAAATAAAT[-/AAATAA]AAATAAGAAAAAAAA | 996 |
rs754489921 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119819 | GCTAAAAATTTCCAA[C/T]ATCCTAAACCCAATT | 996 |
rs754536660 | snp | C/G | 1.93936e-05 | 0.00311391 | intron-variant | CDC27 | GRCh38.p7 | 17:47154865 | CTTAAATTAGAAGGT[C/G]TAAAAGGAAGAGAAT | 996 |
rs754538189 | snp | A/G | 1.73129e-05 | 0.00294213 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171922 | TAAAACTTACTTGCT[A/G]AGATCAACACAACAT | 996 |
rs754628187 | snp | A/C/T | 5.93001e-05 | 0.00544492 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47172063 | GGCTTCTTCTGAGTG[A/C/T]ACTAAAAACAGACAT | 996 |
rs754681505 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149004 | GAATTGCTTGAACTC[A/G]GGAAGCAGAGGTTGC | 996 |
rs754759178 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162317 | TAGATTCCTAATTAA[C/T]GTCTTGCCTCTTCAT | 996 |
rs754767459 | snp | C/T | 0.00166437 | 0.0287996 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138832 | TGTTGTAGAGTAGAT[C/T]TCCATGCCTTCAACT | 996 |
rs754801062 | snp | C/T | 8.47968e-05 | 0.00651085 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141856 | TTCTATACTTACTTG[C/T]ATGTACTCTGAAAGT | 996 |
rs754802933 | snp | G/T | 1.79641e-05 | 0.00299696 | intron-variant | CDC27 | GRCh38.p7 | 17:47122633 | CACTACATTTTTCAT[G/T]AAGTTGTGAGCTTCA | 996 |
rs754827247 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123612 | AGGTCAGGTTTCACC[A/G]TGTTGGTCAGGCTGG | 996 |
rs754871277 | in-del | -/AAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147426 | ACAAACAAACAAACA[-/AAC]AAAAAAAAAAACACT | 996 |
rs754891664 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131398 | TTATCATGGTCAATG[C/T]CATTATAGTCAATAG | 996 |
rs754909214 | snp | A/T | 1.69413e-05 | 0.00291039 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47123928 | TTCTTTGGGAACAAT[A/T]TGTTTCAATTCTTCA | 996 |
rs755044189 | snp | C/G | 5.14708e-05 | 0.00507274 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151819 | ACCTTGTTTGTGGAC[C/G]AGAACTTTGTGTTTG | 996 |
rs755055024 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159245 | GGAGACTCTAGTGTG[C/G]GTCTTGACGAGGTGG | 996 |
rs755055164 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141672 | TTGCAAAGAATTTAA[A/G]TTACTCCTTAACACA | 996 |
rs755060635 | snp | C/T | 1.73896e-05 | 0.00294865 | intron-variant | CDC27 | GRCh38.p7 | 17:47158199 | CCTCTCAACCCCACC[C/T]ACCTACCTATTTCAC | 996 |
rs755142956 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157164 | TCATTCACAATATAT[C/T]ATTTAGTTCAGATCA | 996 |
rs755207023 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126342 | CAAATTAGGCCTCAT[A/C]ATTCAGCGAAGCCCC | 996 |
rs755222441 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125108 | ATTTTTAGTAGAGAT[A/G]GGGTTTCACTAAAGT | 996 |
rs755266844 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167528 | AACCCCTCTTCTTAA[C/T]CAGGCAGGACTAATT | 996 |
rs755289500 | snp | A/C | 1.91951e-05 | 0.00309794 | missense, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120938 | GATTTCCAGAAGTTA[A/C]AATTCATCACTTTCA | 996 |
rs755320944 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144200 | CTCAGCTTGCAGATG[A/G]CCTCTTGTGGGACTT | 996 |
rs755334253 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121896 | AGGCGCCCGCAACCA[C/T]GCCCAGCTAATTTTT | 996 |
rs755358507 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183535 | AGCTTAAATTTTATA[A/G]AGTCTCAAAGATGTC | 996 |
rs755364658 | snp | A/T | 0.00140428 | 0.0264607 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137325 | AATATCATGTTCCCG[A/T]TGCAGACTGAAACAG | 996 |
rs755391686 | snp | A/G | 1.71091e-05 | 0.00292476 | intron-variant | CDC27 | GRCh38.p7 | 17:47142030 | CATCAAACCTTCTAG[A/G]AGAAAACAACATAGT | 996 |
rs755412473 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137448 | ATCAAGCCTCAACTT[A/C]GAACAGAAAGACAAA | 996 |
rs755441004 | snp | G/T | 0.0179199 | 0.0929454 | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157045 | GGTGAAATTACAGCT[G/T]AATCAATATAAGACA | 996 |
rs755449502 | snp | C/G | 3.32801e-05 | 0.00407908 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189151 | TTATCATTACCTGGA[C/G]GGGTTCCTGCAGCAC | 996 |
rs755464253 | snp | A/C | 0.000174795 | 0.00934702 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157114 | GATTCTAAATTCAAT[A/C]TGTTTAATTCCTGAA | 996 |
rs755482871 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153592 | TTCTATTAAGGTAAA[G/T]AGAGTATAACTGTTA | 996 |
rs755498011 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47152549 | CTTCTCTAATTTATT[A/C]CCTTATTTCTATTCA | 996 |
rs755638086 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162344 | TCATCCCTTCAATTC[A/G]TCTATCTAGGCCCCT | 996 |
rs755651588 | snp | A/T | 2.50316e-05 | 0.00353768 | intron-variant | CDC27 | GRCh38.p7 | 17:47132395 | AGTATAAAACAAAGT[A/T]TAATTTTAAAAATAT | 996 |
rs755680074 | snp | C/T | 2.01827e-05 | 0.00317662 | intron-variant | CDC27 | GRCh38.p7 | 17:47171886 | ACAGTGTAAGTAAAA[C/T]AAAATAGCTAGAAAA | 996 |
rs755685863 | snp | C/T | 0.000159494 | 0.00892869 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142249 | GCTGCTTTTTGTAGA[C/T]TAAAGGCCTGAATCT | 996 |
rs755792256 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117757 | TACTAAAAAAGAGTA[C/T]GACCGTTTAAAAATA | 996 |
rs755815361 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119526 | AATAATAACTGTAGG[A/C]CTGTCATTCATAAGA | 996 |
rs755872196 | in-del | -/TT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123404 | ACTTTTTTTTCTACT[-/TT]TTTTTTTTTTTTTTT | 996 |
rs755899726 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136778 | CCTATTATCCAATAA[A/G]TGAATTATGCTATTC | 996 |
rs755932924 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159621 | TGTTGATGGCCCTGC[A/G]GATGGCAGTGGCCAC | 996 |
rs755934908 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176753 | TATCTTAGGTTAGAT[G/T]TGAATATATTGAGTT | 996 |
rs755969130 | snp | A/G | 5.60837e-05 | 0.00529516 | intron-variant | CDC27 | GRCh38.p7 | 17:47154830 | AAAAGTCATCAAGGC[A/G]TATATAAAGCAGCAG | 996 |
rs755981325 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146527 | ACTCCAAGCTGGGAA[C/T]AGCTCATACTTTCAA | 996 |
rs755990415 | in-del | -/AAAAG | 5.41629e-05 | 0.0052037 | intron-variant | CDC27 | GRCh38.p7 | 17:47158156 | TTAAGTAGCAGGAAA[-/AAAAG]AAGAGGAGATGGGAA | 996 |
rs756050252 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172559 | CTTTAACATCAAATA[C/T]ACATTAAATTATATT | 996 |
rs756054404 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128219 | TATTTTTGGTAGAGA[C/T]GGGGTTTCACCCTGT | 996 |
rs756082072 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155350 | TGCTGGGTTCAAATG[A/G]TTCTTGTGCCTCAAC | 996 |
rs756142796 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145624 | GGTCAACCATGTGGC[C/T]GGGCATGGTGGCTCA | 996 |
rs756164323 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183950 | TCTATTGAAAGAAAC[A/T]CTGTGATAAATAGAA | 996 |
rs756175903 | snp | A/C | 6.80712e-05 | 0.00583361 | intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122612 | AAACCTAAAAATAAA[A/C]AGCAGCACTACATTT | 996 |
rs756193769 | snp | A/G | 3.37336e-05 | 0.00410678 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47123901 | CTTTCCTATTAAGAA[A/G]TAAACGAGGGATTCT | 996 |
rs756247874 | snp | G/T | 1.71725e-05 | 0.00293018 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157244 | CAATTGTGTCCTGGG[G/T]TGTTTCCGTAAGAAC | 996 |
rs756329654 | snp | G/T | 1.64808e-05 | 0.00287057 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157339 | CAGTTGCTAAAGTTC[G/T]GTAAAGATGTGAATT | 996 |
rs756351354 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140444 | GCATGGTAACAAGAT[A/G]AAAGACCTACCAGCC | 996 |
rs756435135 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164721 | ACTCCGGAGGCTGAG[A/G]CACGAGAACTGCTTG | 996 |
rs756463142 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156705 | TGCCTGCCTTGGCCT[C/T]CCAAGGTGCTGGGAT | 996 |
rs756524573 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180488 | AGCATTGCTCTTTGT[C/T]CTTTTGTGAAATTTC | 996 |
rs756534531 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129930 | CTGTACTATTTAGCC[-/A]GATAATATTCACATT | 996 |
rs756539347 | snp | C/G | 1.84862e-05 | 0.00304019 | intron-variant | CDC27 | GRCh38.p7 | 17:47137147 | TGTACTTCATTACCA[C/G]TTACCATGCATTATA | 996 |
rs756541507 | snp | A/G | 0.0049014 | 0.0492613 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156940 | GGACTAAGAGCTGCT[A/G]GTCCTCCTAATAAAC | 996 |
rs756570154 | in-del | -/AAAC | 1.72979e-05 | 0.00294086 | intron-variant | CDC27 | GRCh38.p7 | 17:47142046 | AGAAAACAACATAGT[-/AAAC]AAAGGAAAAAACGCA | 996 |
rs756588488 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126158 | TGAAATGGCCCCCTT[A/G]ATTTTCATTTTGGAG | 996 |
rs756596685 | snp | C/T | 1.75922e-05 | 0.00296577 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181576 | CCTTCTGCATAAAGG[C/T]GTTCTGCGAGGAAAA | 996 |
rs756600293 | snp | G/T | | | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189126 | GCCAGCCAAGCCCCA[G/T]AGAAGAAGGTTATCA | 996 |
rs756637766 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166235 | TGTTCTGTTTTCTGG[A/G]AGAGATTATGTAGCA | 996 |
rs756657114 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150938 | TCAGGAAGCTGAGGC[A/G]GGAGAATCACTTGAA | 996 |
rs756754152 | snp | C/T | 1.69315e-05 | 0.00290955 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142013 | ATTTCACGAAGAAGG[C/T]TCATCAAACCTTCTA | 996 |
rs756767422 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148855 | GAGGCCAAGATGGGC[A/G]ATCACCTGAGGTCAG | 996 |
rs756844266 | snp | C/T | 3.30874e-05 | 0.00406726 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129510 | CTCTGATTTTTTCAG[C/T]GCATGTTGAACCTGT | 996 |
rs756861601 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164544 | AAACTACGCTGGACA[C/T]GGTGGCTCATGACTG | 996 |
rs756905792 | snp | C/T | 0.000805887 | 0.0200573 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120899 | ACACGTCAGCACTAG[C/T]CACACATCCAGTTGT | 996 |
rs756905906 | in-del | -/TTATTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132742 | AGCCATTAAAGCAGT[-/TTATTA]TTATTATTATTATTA | 996 |
rs756927073 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159850 | CTCCTCCAGGGACTT[-/G]ATCTTCATGTCCTTG | 996 |
rs756958350 | snp | C/T | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117650 | GCAAATTCGCAGCTG[C/T]TGGTTGGTAAGGGGC | 996 |
rs757035461 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150502 | ATGCTAAAGAACACC[C/T]GGGGTTATCAGAAGC | 996 |
rs757069047 | snp | C/T | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190421 | AGGGGACTGTTTAAA[C/T]TTTGTTTTTCAGCAG | 996 |
rs757179729 | snp | A/G | 0.00290979 | 0.0380319 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169939 | CATGTCCCAACAATG[A/G]AAGAGTAAAGCAAGC | 996 |
rs757184693 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144382 | ATAAAACTCTGGATC[A/G]ACAAATGATAAGCAC | 996 |
rs757268009 | snp | C/T | 5.19386e-05 | 0.00509574 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47170042 | TTCCCCTTCTGCAAG[C/T]CTTTAAAATACAAAT | 996 |
rs757269620 | snp | C/T | 1.71649e-05 | 0.00292953 | intron-variant | CDC27 | GRCh38.p7 | 17:47151964 | AATTATGGGCTGCAC[C/T]GTAAATGATAAAAGA | 996 |
rs757271031 | snp | A/G | 1.67416e-05 | 0.00289318 | intron-variant | CDC27 | GRCh38.p7 | 17:47122429 | AATACTCAAAATCAT[A/G]TGTATGATACTTACT | 996 |
rs757392611 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181025 | GGGAGGCCAAGGCAG[C/G]TGGATCACCTAAGCT | 996 |
rs757433814 | snp | A/T | 1.6577e-05 | 0.00287893 | synonymous-codon, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122583 | GGCGAGGTGCGTTTG[A/T]CCTAACTTCTTGTAA | 996 |
rs757436293 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138682 | CTTGGTTCATCTCTA[C/T]CTGTTGAGGGTGATC | 996 |
rs757439078 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184970 | CCAAAAAGAACAACG[C/G]TCCTCTCCCTCTCCC | 996 |
rs757464412 | snp | C/T | 3.32945e-05 | 0.00407997 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157235 | AGACACTTACAATTG[C/T]GTCCTGGGGTGTTTC | 996 |
rs757468709 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155249 | TTCTTCTAGCATATA[C/T]GTATATATTTTTTTG | 996 |
rs757476278 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153937 | AAATAAAAGTTAAAA[A/G]AATTAGCTGGGTGTG | 996 |
rs757498494 | in-del | -/CTGGCAGATTTTTATCCAAG/CTGGCAGATTTTTATCCAAGTC/CTGGCAGATTTTTATCCAAGTCTG/CTGGCAGATTTTTATCCAAGTCTGTTAAG/CTGGCGAA | | | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47137362 | CAGCACACCAGGCCT[lengthTooLong]TAAAAAAATGGGAAC | 996 |
rs757559046 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171423 | TCCATCTCTTACAGT[A/G]CAGAAAAGAATTGAA | 996 |
rs757560801 | snp | C/G | 3.38966e-05 | 0.00411669 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143935 | CTTCTTCGAGGCAGT[C/G]CGTTTGGGGGAGATG | 996 |
rs757568010 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140139 | TATATAGGAATAGCT[G/T]AACGATTTGTAACTT | 996 |
rs757615823 | snp | C/T | 1.64817e-05 | 0.00287064 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157330 | TTGGGCAGACAGTTG[C/T]TAAAGTTCTGTAAAG | 996 |
rs757622381 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186339 | AAGAGTACTCCTTCA[C/T]CATCTAATGATCTCT | 996 |
rs757639018 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178983 | ATTTTGTATTTTTTA[G/T]TAGAGATGGGGTTTC | 996 |
rs757693142 | snp | A/C | 3.30055e-05 | 0.00406222 | intron-variant | CDC27 | GRCh38.p7 | 17:47137111 | TAGTAAGTACCAGCA[A/C]CATCAATACGACTTT | 996 |
rs757729605 | in-del | -/A | 0 | 0 | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47143984 | CTGAGGTGTTGTACT[-/A]AAAAAAAAATTATAA | 996 |
rs757731447 | snp | A/G | 3.9326e-05 | 0.00443412 | intron-variant | CDC27 | GRCh38.p7 | 17:47172089 | GACATTTTTTAAAAA[A/G]GCTATTGTTCAGTAT | 996 |
rs757745638 | snp | A/G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124812 | AAAAAGGTAAATAAC[A/G/T]TCAAGATATTATTGT | 996 |
rs757828897 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138003 | AAGGGTTTTGCCATG[C/T]TGCCGAGGCTGGTCT | 996 |
rs757855361 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162368 | GGCCCCTTCTGTCTC[A/G]TAATACTAACCATAG | 996 |
rs757878045 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140771 | GAAACATGGGTTTTG[C/T]AGCAATGAATAAGAC | 996 |
rs757884277 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123026 | ATGTGCTCTAAACTC[A/T]TTCTAAGGGTAGGAC | 996 |
rs757942944 | snp | C/T | 3.34997e-05 | 0.00409252 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141891 | AATAGGCCCTTCCAA[C/T]TTGGCACAGTACCCA | 996 |
rs757950884 | in-del | -/ACAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177858 | TTTATATGTGTGTGT[-/ACAC]ACACACACACACACA | 996 |
rs757959361 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148685 | AGAAAAGACATATTA[C/G]TACATATAGAGGAAC | 996 |
rs757962167 | snp | C/G | 2.32296e-05 | 0.00340797 | intron-variant | CDC27 | GRCh38.p7 | 17:47154892 | GAATGGCAAATCAGT[C/G]TTAGGGACAGTGAGG | 996 |
rs758017622 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130121 | AATCTGAGCACGTTG[C/G]GAGGCCAAGGCAGGT | 996 |
rs758042275 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181938 | CCCTTATAAACTGCT[C/T]GTCCCTAAAGATCCA | 996 |
rs758052049 | snp | C/G | 1.71026e-05 | 0.00292421 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156926 | ACCTTGGGGTTAATG[C/G]ACTAAGAGCTGCTGG | 996 |
rs758122672 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171770 | ATATAAATAATGCCA[G/T]AGGCAACAGTGTAAA | 996 |
rs758141014 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187228 | AGAGTACTTTAAGGA[C/T]AAACAGGAAACCTGA | 996 |
rs758203179 | snp | G/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189031 | CAGGACACGGCAGCA[G/T]GGGAGGCGGGAGAAG | 996 |
rs758254039 | snp | A/C | 0.000726186 | 0.0190412 | stop-gained, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142002 | AACCTTTCCCCATTT[A/C]ACGAAGAAGGCTCAT | 996 |
rs758324071 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151647 | AAACTCAACTCAAAA[C/T]TACATTAGTGTTGTA | 996 |
rs758356079 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123793 | AGTTTAATTTGCTCA[A/G]TAGATATGTACAGGA | 996 |
rs758367976 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139266 | ATTACAGAATAACTC[-/T]TTTTTTTTTTTTTTT | 996 |
rs758401119 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183680 | CTGTATTAATTTAGG[A/C]GAGTATTTGAGTGAT | 996 |
rs758407702 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173582 | TTAACTCCCAGTCAC[A/G]GTAATGCTGTCTCAA | 996 |
rs758458254 | snp | C/T | 1.70136e-05 | 0.00291659 | intron-variant | CDC27 | GRCh38.p7 | 17:47151954 | AAGGTTTGTGAATTA[C/T]GGGCTGCACTGTAAA | 996 |
rs758473592 | snp | A/G | 0.00679955 | 0.0579098 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137330 | CATGTTCCCGTTGCA[A/G]ACTGAAACAGTTCCC | 996 |
rs758491179 | in-del | -/CTGAAACAGAAAATTTCTACCA | 0.0010022 | 0.0223628 | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47157125 | CAATCTGTTTAATTC[-/CTGAAACAGAAAATTTCTACCA]AGTCATTCACAATAT | 996 |
rs758502776 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126359 | TTCAGCGAAGCCCCA[A/G]GCTCATACCCAAAAA | 996 |
rs758559512 | snp | C/G | 1.67103e-05 | 0.00289048 | intron-variant | CDC27 | GRCh38.p7 | 17:47138690 | ATCTCTATCTGTTGA[C/G]GGTGATCAAAAAGGT | 996 |
rs758561443 | snp | A/G | 1.88809e-05 | 0.00307248 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120944 | CAGAAGTTAAAATTC[A/G]TCACTTTCAGCTGCA | 996 |
rs758595317 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176144 | TGGCCTTCTCTTAAA[C/T]TTACAATACCTGAAT | 996 |
rs758681068 | in-del | -/AAACA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147425 | AACAAACAAACAAAC[-/AAACA]AAAAAAAAAACACTA | 996 |
rs758698620 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184870 | GGTGTGGGCCTTCCC[G/T]TAAAAGAACACCCAG | 996 |
rs758699741 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153693 | ATATATAGAACCTAA[C/T]TTAATTCTCACAGAA | 996 |
rs758734901 | in-del | -/A | 1.6922e-05 | 0.00290873 | intron-variant | CDC27 | GRCh38.p7 | 17:47151777 | AAGTTTTATGCCAAG[-/A]AAAGTTGAATAATTA | 996 |
rs758786782 | snp | A/G | 1.64958e-05 | 0.00287187 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132296 | TGAACTTTGAGGGTT[A/G]ATATCAAGCGCTTTT | 996 |
rs758795699 | snp | G/T | 3.37103e-05 | 0.00410537 | intron-variant | CDC27 | GRCh38.p7 | 17:47122416 | AGGTAACTTTCTAAA[G/T]ACTCAAAATCATATG | 996 |
rs758807340 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121159 | ATCCTCATATCCTTT[A/C]ATAAAATGCAACTCA | 996 |
rs758841339 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134038 | TGCAGGTGTGAGCTA[-/C]CCACCCCCAGCCTTC | 996 |
rs758892107 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138506 | AAATTTAACGTAGTC[A/G]AATCTCGATAAATCC | 996 |
rs758928574 | snp | C/T | 5.55232e-05 | 0.00526863 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142382 | TAGTTTTACTTTTTG[C/T]TTTTCTGTTTGGGAT | 996 |
rs759092797 | in-del | -/G | 0.001278 | 0.0252461 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156970 | CTTCGACCAGTTTTT[-/G]GTTTATTTTGAACCT | 996 |
rs759107956 | snp | A/T | 3.2676e-05 | 0.0040419 | intron-variant | CDC27 | GRCh38.p7 | 17:47143996 | TACTAAAAAAAAATT[A/T]TAAAGGAAGACATTA | 996 |
rs759117834 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139792 | ATTATCCTTTCCTTT[A/G]CAGCACTCTCTTGAC | 996 |
rs759149334 | snp | C/T | 1.94835e-05 | 0.00312112 | intron-variant | CDC27 | GRCh38.p7 | 17:47181540 | TCATTTATCATTCTA[C/T]AGCAATGAATAGATT | 996 |
rs759154493 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127764 | CTGAAGTGCAGTGGC[A/G]CGAAAACAGCTCACT | 996 |
rs759160910 | snp | A/G | 3.47307e-05 | 0.00416703 | intron-variant | CDC27 | GRCh38.p7 | 17:47157387 | TCTGGCTTTTCACCT[A/G]TGAAGACAAAAAAAA | 996 |
rs759162072 | snp | A/C | 1.65299e-05 | 0.00287483 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137184 | AGGATTGACTCTGAT[A/C]GCATTTCGAAAACAA | 996 |
rs759191311 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181466 | AGAAAAACAACAAGA[C/T]GATGATAGCTAGAAT | 996 |
rs759209782 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140853 | TAGGTATCCTCTGTA[C/T]GTATTCCCTGTGGGA | 996 |
rs759226197 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156213 | ACACCATCTCGGCTC[A/T]CTGCAACCTCTGTCT | 996 |
rs759246580 | snp | C/T | 3.31791e-05 | 0.00407289 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157006 | GATAATATGGAAGTT[C/T]CTGTTCCCAGTGGGA | 996 |
rs759251820 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122832 | GTGCCCACCACCACC[C/T]CTGGCTAATTTTTGT | 996 |
rs759315738 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164076 | GCCCCCATAAGATTA[C/T]AATGCCATATTTCTA | 996 |
rs759378683 | in-del | -/TC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170150 | GAGACACAAATTTTT[-/TC]TCTCTCTCTCTTTCC | 996 |
rs759403675 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179776 | TCCAAGTGCCAAGCA[C/T]TGTATCAGGTACATA | 996 |
rs759539830 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148575 | GATCCAAGAAGCTCA[A/G]TAAATCCAAAGGCCG | 996 |
rs759561642 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174914 | TGAGCCGAGATCATG[C/T]CACTGCACTCCAGCC | 996 |
rs759628999 | snp | C/T | 1.648e-05 | 0.0028705 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169998 | TCATGGCTTTTCTGC[C/T]TATTAAACACTCCAC | 996 |
rs759652195 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118777 | CAGAAAGTGTTACTA[C/T]GTGGGAAATAAGGCT | 996 |
rs759655850 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160228 | TGCTGCCTCTCTAGC[-/T]TTTTTTTTTTTTTTT | 996 |
rs759696309 | snp | C/T | 3.51568e-05 | 0.00419251 | intron-variant | CDC27 | GRCh38.p7 | 17:47142063 | ACAAAGGAAAAAACG[C/T]AATAAACTAGTCTGC | 996 |
rs759700352 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137691 | CTGTGGGCTAGTTTA[A/G]TGTAGTGCAAGAAGC | 996 |
rs759705637 | in-del | -/GTT | 1.67433e-05 | 0.00289333 | intron-variant | CDC27 | GRCh38.p7 | 17:47129343 | AAAACAAGGGATAAC[-/GTT]GTTTTTAAGCAATAC | 996 |
rs759723257 | snp | G/T | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129437 | AGGCTCTGTGAAATT[G/T]GCATAGAGGGTTCTT | 996 |
rs759772809 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120423 | GGTAATTTACATTCC[C/T]TGGCAATCAAGTCAC | 996 |
rs759777725 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127699 | AGCCACTGTGCCTGG[A/C]CCTATTTTTTTTTTG | 996 |
rs759806920 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145443 | ATATAATAAAGAATT[C/T]GTCTGGTCCACGTCC | 996 |
rs759826039 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184623 | CTTAAAATCAAGCTT[C/T]GCTCAGAACATCATT | 996 |
rs759900387 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159956 | TCCCGGCCCCATCCA[C/T]GGCTGCGACCCCAGC | 996 |
rs759936019 | snp | A/G | 2.57172e-05 | 0.0035858 | intron-variant | CDC27 | GRCh38.p7 | 17:47154647 | CTTTAATCAATTCCC[A/G]AACTGCATTTTACAT | 996 |
rs759973282 | snp | C/T | 8.35694e-05 | 0.00646357 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138745 | TTAACATACCTCTGG[C/T]GAATTTTTATCCATG | 996 |
rs760024854 | snp | A/G | 5.07722e-05 | 0.0050382 | intron-variant | CDC27 | GRCh38.p7 | 17:47122396 | CCTACAAATCCTTAT[A/G]CAAAAGGTAACTTTC | 996 |
rs760087136 | snp | C/T | 8.39384e-05 | 0.00647782 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142362 | TTGAGTTATTCCTCC[C/T]TTATTAGTTTTACTT | 996 |
rs760091347 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186254 | AATCTAAATTTCTCA[C/T]TGAGTAGCCAAAATA | 996 |
rs760232211 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179457 | ACTCTTGGGAAAGCG[C/G]AATCAGACAGATTAC | 996 |
rs760299284 | snp | A/G | 1.68755e-05 | 0.00290473 | intron-variant | CDC27 | GRCh38.p7 | 17:47157195 | TTCTTTGTAGTTTTC[A/G]TAATATTTTGAACAC | 996 |
rs760367183 | snp | C/T | 1.6563e-05 | 0.00287771 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137166 | CCATGCATTATAATG[C/T]CTAGGATTGACTCTG | 996 |
rs760381439 | snp | C/T | 2.05139e-05 | 0.00320258 | intron-variant | CDC27 | GRCh38.p7 | 17:47181528 | CATATATGTTATTCA[C/T]TTATCATTCTACAGC | 996 |
rs760406306 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178061 | AAAAATACATGCTTA[A/C]AATGGGGGAAGGGAA | 996 |
rs760442171 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122724 | TATTACCCAGGCTAG[A/G]GTGCAATGGCACGAT | 996 |
rs760461040 | in-del | -/TCTC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166488 | TATAAGTAATGGTGT[-/TCTC]TCTCTTTCTTTTTTG | 996 |
rs760470136 | in-del | -/T | 8.72892e-05 | 0.00660583 | intron-variant | CDC27 | GRCh38.p7 | 17:47137123 | CACCATCAATACGAC[-/T]TTTGTCTTTGTACTT | 996 |
rs760482419 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120852 | ACACCGCCAGCTCAA[C/G]AGTAAAGACTCAGTA | 996 |
rs760552191 | snp | G/T | 2.57616e-05 | 0.00358889 | intron-variant | CDC27 | GRCh38.p7 | 17:47137128 | ATCAATACGACTTTG[G/T]CTTTGTACTTCATTA | 996 |
rs760573996 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163859 | AACCTCTGCCTCCTG[C/G]ATTCAAGTGATTCTC | 996 |
rs760632084 | snp | C/T | 3.94578e-05 | 0.00444155 | intron-variant | CDC27 | GRCh38.p7 | 17:47156898 | GCACATTTGAAAGTA[C/T]CTTGTTTGACTTACC | 996 |
rs760675537 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160741 | TCCTCAACTGAAACT[A/C]TCAGGTAAAATGTAT | 996 |
rs760691811 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188739 | AACCTCCGTAAACTT[A/G]CCCTACCGTCACGAA | 996 |
rs760702321 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122553 | TAAATCCATAGCCCA[A/G]GAGAAATTCATCAGG | 996 |
rs760805313 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118712 | TCGGGTTGTTTGATC[C/T]CCATTCCATGCAAAA | 996 |
rs760813902 | snp | A/C | 0.000100155 | 0.00707585 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141984 | ATGAACACAAAGCTA[A/C]ATAACCTTTCCCCAT | 996 |
rs760835541 | snp | A/G | 1.7412e-05 | 0.00295055 | intron-variant | CDC27 | GRCh38.p7 | 17:47157426 | TGTCTCTGAGGAAGT[A/G]AGGAATACATGTTTT | 996 |
rs760865257 | snp | A/G | 1.70472e-05 | 0.00291947 | intron-variant | CDC27 | GRCh38.p7 | 17:47141838 | AAGGCATATATAACC[A/G]TTTTCTATACTTACT | 996 |
rs760899593 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143350 | ACATAACCATAGTAT[A/G]TCATCATACCCAGGA | 996 |
rs760975756 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188540 | TTCCACCTCCTCCCC[G/T]GGTATTGGTGCTTGC | 996 |
rs761007595 | in-del | -/CC | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158279 | TGGTAACATTCTGAT[-/CC]CCTTTGGCAAGCCGA | 996 |
rs761018685 | snp | A/T | 1.64811e-05 | 0.00287059 | intron-variant | CDC27 | GRCh38.p7 | 17:47154629 | ATTGAAATAAACAAG[A/T]TGCTTTAATCAATTC | 996 |
rs761041557 | snp | C/G | 9.90426e-05 | 0.00703644 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129419 | CATTTGCAAATAAAA[C/G]TGAGGCTCTGTGAAA | 996 |
rs761060631 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145667 | CAGCACTTTGGCAGG[C/T]CAAGGCAGGCGGATC | 996 |
rs761066538 | snp | C/T | 1.958e-05 | 0.00312884 | intron-variant | CDC27 | GRCh38.p7 | 17:47158341 | TAAATAAGCTACAAA[C/T]CCCAAAACCTGTATC | 996 |
rs761074466 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159923 | TTGGCCTTGCCTCCA[C/T]GAGCTCCGTGGCCTC | 996 |
rs761087556 | snp | C/T | 6.67847e-05 | 0.00577822 | missense, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151929 | ACAGACTGTAAAACA[C/T]GAAAAGTCTAAGGTT | 996 |
rs761147763 | snp | A/T | 3.37958e-05 | 0.00411056 | intron-variant | CDC27 | GRCh38.p7 | 17:47129564 | CTCCCTCTTGATATT[A/T]ATGAAGAAAGGTGAG | 996 |
rs761166548 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170918 | CCAGCCTGGGCAACA[C/T]AGTGAGACCCCATCT | 996 |
rs761170015 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182933 | CAGAAGGCTGAGCTG[C/G]GAAGACTGCTTGAGT | 996 |
rs761203169 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145979 | CCTCTGGGAAGGAAA[-/T]TTGAGTTCAATCATG | 996 |
rs761222826 | snp | A/G | 1.7161e-05 | 0.0029292 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157100 | ACTTTGAATTGGAAG[A/G]TTCTAAATTCAATCT | 996 |
rs761249462 | snp | A/C | 0.00684594 | 0.0581042 | intron-variant | CDC27 | GRCh38.p7 | 17:47137370 | CCAGGCCTTAAAAAA[A/C]TGGGAACAAAAACCA | 996 |
rs761253109 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145303 | TGAGAAAGCCAAAGC[A/G]GCCAGAATTTGCAAG | 996 |
rs761420933 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181696 | CTTTCAAGGTAACTA[C/G]TAGCACACAGCCTTA | 996 |
rs761441999 | in-del | -/G | 1.65026e-05 | 0.00287246 | frameshift-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137282 | AATTTGGATCAACTT[-/G]GATAGCTCTCTGGAA | 996 |
rs761472581 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127204 | GGAATTTGAGGCTTC[A/G]GTGAGCTATGATTGC | 996 |
rs761533993 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47152295 | ATTCTCAAGATTTAT[A/G]ATTTATCTCATTATA | 996 |
rs761556846 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174959 | ACTCGGTCGAAACAG[G/T]ACTATCGAAACAGGA | 996 |
rs761573434 | snp | A/C | 3.56087e-05 | 0.00421937 | intron-variant | CDC27 | GRCh38.p7 | 17:47143850 | GCAGGCGAAGCATTA[A/C]GTAAATGTGACATAC | 996 |
rs761599940 | in-del | -/T | 1.66838e-05 | 0.00288818 | intron-variant | CDC27 | GRCh38.p7 | 17:47138696 | ATCTGTTGAGGGTGA[-/T]CAAAAAGGTAACTAT | 996 |
rs761626228 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167072 | GTTGGCCTGGCTGGT[A/C]TCAAATTCCCCACCT | 996 |
rs761626815 | snp | A/T | 5.56468e-05 | 0.00527449 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142340 | CCAGGCTATCATTTA[A/T]GTTAGGTTGAGTTAT | 996 |
rs761628986 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136459 | AAACTACCACAGAGT[G/T]ATGGCTTCAGAATTA | 996 |
rs761645846 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158142 | TTGCTCTCCAAAAAT[G/T]AAGTAGCAGGAAAAA | 996 |
rs761660767 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153139 | TATTTATCAAAGAAC[C/T]ATGTACACTGCACTC | 996 |
rs761668489 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137991 | TTTTTTGTGGAGAAG[A/G]GTTTTGCCATGTTGC | 996 |
rs761708467 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177780 | TTCCATAGGTAGCAA[C/T]TACTTATGAAAAAAA | 996 |
rs761718904 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181273 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAAACC | 996 |
rs761802256 | snp | C/T | 5.81945e-05 | 0.00539387 | intron-variant | CDC27 | GRCh38.p7 | 17:47137123 | GCACCATCAATACGA[C/T]TTTGTCTTTGTACTT | 996 |
rs761803692 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187780 | TAACTTGAGTAATCT[G/T]CTTATCTATTTAAGT | 996 |
rs761873103 | snp | C/T | 1.70702e-05 | 0.00292144 | intron-variant | CDC27 | GRCh38.p7 | 17:47141831 | CTCTAGAAAGGCATA[C/T]ATAACCATTTTCTAT | 996 |
rs761904926 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148376 | TAAACACTATCCAAA[A/G]TGAAACACGGAGAGG | 996 |
rs761909798 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172996 | AAATGAAAATTTTTG[C/T]GTCCCATCTCATACC | 996 |
rs761918253 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186922 | AGTTTTTTTTTTAAT[A/G]AAGACAGTATCTTAT | 996 |
rs761967390 | snp | C/T | 8.43437e-05 | 0.00649344 | intron-variant | CDC27 | GRCh38.p7 | 17:47156881 | GATCATTTGGTATTA[C/T]AGCACATTTGAAAGT | 996 |
rs762034350 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156534 | CTCACTACAACCTCC[A/G]CCTCCCGGGTTCAAG | 996 |
rs762104127 | snp | A/G | 1.71646e-05 | 0.0029295 | intron-variant | CDC27 | GRCh38.p7 | 17:47123877 | TGGGACCATGACCCC[A/G]GTCTTTACCTTTCCT | 996 |
rs762165131 | snp | A/T | 5.4761e-05 | 0.00523235 | intron-variant | CDC27 | GRCh38.p7 | 17:47158319 | CTGTGGAGAGAAACA[A/T]GTAGATTAAATAAGC | 996 |
rs762185938 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188197 | TGACTCAATGACAGC[A/G]GTTGATAGAGGTCAA | 996 |
rs762237672 | snp | A/G | 1.69026e-05 | 0.00290706 | intron-variant | CDC27 | GRCh38.p7 | 17:47157400 | CTGTGAAGACAAAAA[A/G]AAAAAAAGTTTGTCT | 996 |
rs762318397 | in-del | -/GTAA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171508 | TGACTTGGTTTAACT[-/GTAA]TGTGCAAAAGAAGTA | 996 |
rs762325771 | snp | G/T | 0.000543497 | 0.0164758 | intron-variant | CDC27 | GRCh38.p7 | 17:47151757 | TTAAAGAAATGTAAA[G/T]AATCAAGTTTTATGC | 996 |
rs762398259 | snp | G/T | 1.65392e-05 | 0.00287564 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151909 | CAGTTTGGCCGATTC[G/T]GGCAACAGACTGTAA | 996 |
rs762406031 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140999 | CTTCATTTTTCTTCA[A/T]GACTTATTGCTACCT | 996 |
rs762450197 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158536 | TGCCTTCTTGAATAT[C/T]ACTATTACTTTAAAC | 996 |
rs762452614 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150903 | TGGGTGTGGTGACAC[-/A]TGCCTATAATCCCAG | 996 |
rs762459896 | in-del | -/G | 0.015527 | 0.0867318 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157042 | TCAGGTGAAATTACA[-/G]CTGAATCAATATAAG | 996 |
rs762482584 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180019 | TGTAACTCCAGCTCT[C/T]TGGGAGGCTGAGGCA | 996 |
rs762526779 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124409 | CTGCCTCAGCCTCCC[A/G]CGTAACTGGGATTAC | 996 |
rs762548758 | snp | A/G | 0.000315376 | 0.0125534 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157021 | CCTGTTCCCAGTGGG[A/G]CAGTATCAGGTGAAA | 996 |
rs762574139 | in-del | -/GGCG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125270 | TTTTTTTTTTGAGAT[-/GGCG]TTTCACTCTATCACC | 996 |
rs762582140 | snp | A/G | 0.00174675 | 0.0295013 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137206 | CGAAAACAAGCTAAT[A/G]CTTTGTCCAATTCTT | 996 |
rs762586670 | in-del | -/G | 1.6501e-05 | 0.00287232 | intron-variant | CDC27 | GRCh38.p7 | 17:47154808 | AGAGGTTGAAATCAA[-/G]GTGTCAAAAAGTCAT | 996 |
rs762607163 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143105 | AGCCTCCCAAGCAGC[C/T]GGGATCAAAGAGTAC | 996 |
rs762638148 | in-del | -/A | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47139983 | AAAGGTCTAGGTAAT[-/A]AAAAAAAAAAGAAAG | 996 |
rs762667966 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182645 | GAAATCCAATGTTTT[C/G]AAAATTCATTCTTGA | 996 |
rs762719805 | snp | A/T | 0.000434068 | 0.0147257 | intron-variant | CDC27 | GRCh38.p7 | 17:47157139 | CCTGAAACAGAAAAT[A/T]TCTACCAAGTCATTC | 996 |
rs762725641 | snp | C/T | 8.3764e-05 | 0.00647109 | intron-variant | CDC27 | GRCh38.p7 | 17:47142187 | TACTTAAAATAAGTA[C/T]ATAATAAAATACAAA | 996 |
rs762733016 | snp | A/C | 1.67967e-05 | 0.00289794 | intron-variant | CDC27 | GRCh38.p7 | 17:47132222 | TATTTCAAAAGGGAG[A/C]TTAATAGAGTATTAA | 996 |
rs762760080 | snp | C/T | 2.15431e-05 | 0.00328194 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120887 | GAGGGACAAGAAACA[C/T]GTCAGCACTAGTCAC | 996 |
rs762770987 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157754 | CAGTAAAGGTTGAAG[C/T]CCTTCTATATATACA | 996 |
rs762790656 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166958 | CTCCCAGGTTCAAGC[A/C]ATTCTCGTGCCTCAG | 996 |
rs762807784 | snp | C/T | 2.41112e-05 | 0.00347203 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142330 | TTTGTAATTTCCAGG[C/T]TATCATTTATGTTAG | 996 |
rs762843932 | snp | A/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190194 | GAAGAGTAGGGGGTC[A/G]GAAATTCAGAGGCCT | 996 |
rs762942069 | in-del | -/AG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175031 | AAGAAAGAGAGAAAG[-/AG]AGAGAGAGAGGAAGG | 996 |
rs763032270 | snp | A/C | 7.14839e-05 | 0.00597803 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154781 | TCTAATGGCAAAATC[A/C]CAAAACTGAGAAGAG | 996 |
rs763080445 | in-del | -/TAGT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174601 | AAATCAATCGTGTAC[-/TAGT]TAGTTAAATTATGCT | 996 |
rs763088497 | snp | A/G | 0.00010817 | 0.00735347 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154681 | AAATACCTTTTTTGA[A/G]GGGGCTCCGGTGGAT | 996 |
rs763114815 | snp | A/G | 1.68238e-05 | 0.00290028 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132356 | TTCTTGCTTGTAATA[A/G]ATCATTCCTAAACCA | 996 |
rs763225740 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167326 | GCTCTTTAGGATTAT[C/T]TCTCCAACATTCCTT | 996 |
rs763239871 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146387 | CTGTGATCTTAACCT[A/G]TGGTGTCTGTGCTAA | 996 |
rs763260920 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186824 | CTATGCCTAGTAATA[C/T]CATCAACTCTGAGGC | 996 |
rs763314930 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136557 | TGGTGTTGAGGCAGA[A/T]ATAGGACCAAACTTT | 996 |
rs763332204 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164145 | ATACTGTTATAACTG[-/C]CTACAGTATTCAGTA | 996 |
rs763340610 | snp | A/C | 0.00190854 | 0.0308322 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138783 | AGTCTTTTGACAGAA[A/C]TGAAAGAGCAACATC | 996 |
rs763355545 | snp | C/T | 2.02624e-05 | 0.00318289 | intron-variant | CDC27 | GRCh38.p7 | 17:47138925 | GTAAGAGAAAACAAG[C/T]TGATACAATTTATAT | 996 |
rs763435789 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125197 | AGTGCTAGGATTACA[G/T]TTGTGAGCCACTGCA | 996 |
rs763450688 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130747 | CCAGGCGTGGTGTCG[A/G]GCACCTGTAATCCCA | 996 |
rs763455624 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122061 | TATAATTTTAATTAA[A/T]GCCTTTCACCAAGTT | 996 |
rs763480851 | snp | A/G | | | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47170041 | GTTCCCCTTCTGCAA[A/G]CCTTTAAAATACAAA | 996 |
rs763483994 | in-del | -/C | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190385 | TTCTGCTCCCCTTCT[-/C]CCCCCCAAAAAGAGT | 996 |
rs763506277 | snp | A/C/T | 3.29755e-05 | 0.00406038 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157298 | AACTATGATTAGGTA[A/C/T]TTGTGTTGTGCAAGA | 996 |
rs763586461 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172722 | AGGAAATGCCCCCTG[C/G]CTTCTTAATGCAAGT | 996 |
rs763604837 | snp | A/C/G | 3.33735e-05 | 0.00408483 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189107 | CTGCTTCCCGACCGA[A/C/G]GCTGCCAGCCAAGCC | 996 |
rs763689938 | snp | C/G | 0.000119253 | 0.00772091 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189214 | AGTGCCTCAGGCCCC[C/G]CCTGTAGCGGCTCCG | 996 |
rs763708643 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125960 | TATAATTGTTATCAA[C/T]ATTTCATGCAACCAG | 996 |
rs763715703 | snp | C/T | 1.68553e-05 | 0.00290299 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142004 | CCTTTCCCCATTTCA[C/T]GAAGAAGGCTCATCA | 996 |
rs763717590 | snp | C/T | 0.000514677 | 0.0160335 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157086 | TGTATTCAAGGAGTA[C/T]TTTGAATTGGAAGAT | 996 |
rs763754940 | snp | A/G | 0.000330677 | 0.0128541 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137308 | TGGAAGAATTTAATT[A/G]CAATATCATGTTCCC | 996 |
rs763768990 | snp | C/T | 1.65982e-05 | 0.00288077 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157022 | CTGTTCCCAGTGGGA[C/T]AGTATCAGGTGAAAT | 996 |
rs763775820 | in-del | -/TG | 0.00116748 | 0.0241324 | intron-variant | CDC27 | GRCh38.p7 | 17:47137126 | CCATCAATACGACTT[-/TG]TCTTTGTACTTCATT | 996 |
rs763803915 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165833 | TTTTAATAAGGTATG[A/G]GGTTTAAGTCAATGC | 996 |
rs763841421 | snp | C/T | 2.14208e-05 | 0.00327261 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120893 | CAAGAAACACGTCAG[C/T]ACTAGTCACACATCC | 996 |
rs763898472 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135103 | GTTATACAGCTAATA[-/T]AAGATTCTAACCAGG | 996 |
rs763898842 | snp | A/C | 1.77729e-05 | 0.00298096 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132374 | CATTCCTAAACCATA[A/C]CTGAAAGTATAAAAC | 996 |
rs764067214 | snp | A/G | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117538 | TTCTTTCAGATCCTG[A/G]CCTTTTTAAATAGAT | 996 |
rs764095522 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161994 | CCTTTGCCTGATGGG[C/G]AATTTCATCTAGGTT | 996 |
rs764104671 | snp | C/T | 3.35638e-05 | 0.00409643 | intron-variant | CDC27 | GRCh38.p7 | 17:47132227 | CAAAAGGGAGATTAA[C/T]AGAGTATTAATGTTT | 996 |
rs764121614 | in-del | -/GGTT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171602 | TCAAGTGAGCTGGTG[-/GGTT]GGTTTTCAGGCTTAC | 996 |
rs764207047 | snp | A/T | 1.67189e-05 | 0.00289122 | stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171970 | GCATTGCGGTGTAGT[A/T]CAACTGTGTCCTTTC | 996 |
rs764245114 | snp | A/G/T | 0.000133508 | 0.00816931 | intron-variant | CDC27 | GRCh38.p7 | 17:47138692 | CTCTATCTGTTGAGG[A/G/T]TGATCAAAAAGGTAA | 996 |
rs764249323 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123401 | TCTACTTTTTTTTCT[-/A]CTTTTTTTTTTTTTT | 996 |
rs764277351 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183078 | GGAATAAAATTACTG[A/G]GTTGTTGAATATGCA | 996 |
rs764332222 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186867 | AACAATTTTCCAACT[C/T]ACTCTCATTGCTTTC | 996 |
rs764348666 | snp | C/T | 0.00193103 | 0.0310127 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138784 | GTCTTTTGACAGAAC[C/T]GAAAGAGCAACATCT | 996 |
rs764353513 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172822 | TCCAGGGTCTACAGA[A/G]GCAACAACAAAGAGG | 996 |
rs764401828 | snp | A/G | 2.44251e-05 | 0.00349456 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154783 | TAATGGCAAAATCCC[A/G]AAACTGAGAAGAGGT | 996 |
rs764458660 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129215 | TCCTAAATATCCACA[C/T]ACCTATCCTTCCTAT | 996 |
rs764463300 | snp | A/G | 1.67209e-05 | 0.00289139 | intron-variant | CDC27 | GRCh38.p7 | 17:47157217 | TTTGAACACTAGAAT[A/G]TAAGACACTTACAAT | 996 |
rs764471836 | in-del | -/C | 0.00010007 | 0.00707284 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157040 | TATCAGGTGAAATTA[-/C]AGCTGAATCAATATA | 996 |
rs764526546 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171052 | GCAGTGAGCCATCAT[C/T]ACCCCACTGCACTCC | 996 |
rs764543429 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157316 | GTGTTGTGCAAGAGT[C/T]GGGCAGACAGTTGCT | 996 |
rs764676965 | in-del | -/GAT | 5.54816e-05 | 0.00526666 | intron-variant | CDC27 | GRCh38.p7 | 17:47142203 | ATAATAAAATACAAA[-/GAT]AATATTAAGCATTTA | 996 |
rs764772750 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178554 | ATAAATAAAAATAAG[A/G]AAAAAAAAAAAAAAC | 996 |
rs764796745 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139849 | TCAATTTTTTTCCTC[A/T]TCACATTCACAGCTC | 996 |
rs764826125 | in-del | -/A | 0.000130052 | 0.00806283 | intron-variant | CDC27 | GRCh38.p7 | 17:47138898 | CTTTCAGCCTGAAAT[-/A]AAAAAAAACTAGTAA | 996 |
rs764858700 | snp | G/T | 1.65165e-05 | 0.00287367 | intron-variant | CDC27 | GRCh38.p7 | 17:47181684 | CATACATACAGACTT[G/T]CAAGGTAACTACTAG | 996 |
rs764881133 | in-del | -/GCTCTGGAGGATTTTTAT | 0.000259693 | 0.0113921 | cds-indel, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137359 | CTGCAGCACACCAGG[-/GCTCTGGAGGATTTTTAT]CCTTAAAAAAATGGG | 996 |
rs764908219 | snp | A/C | 1.95762e-05 | 0.00312853 | intron-variant | CDC27 | GRCh38.p7 | 17:47137136 | GACTTTGTCTTTGTA[A/C]TTCATTACCACTTAC | 996 |
rs764910004 | snp | C/T | 1.85734e-05 | 0.00304735 | intron-variant | CDC27 | GRCh38.p7 | 17:47181550 | TTCTACAGCAATGAA[C/T]AGATTTCAAACCTTC | 996 |
rs764910434 | snp | C/T | 6.6368e-05 | 0.00576017 | intron-variant | CDC27 | GRCh38.p7 | 17:47144029 | ATTTTACTTGATTTA[C/T]GACCATTAACCATTG | 996 |
rs764946481 | snp | C/T | 1.65916e-05 | 0.00288019 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157012 | ATGGAAGTTCCTGTT[C/T]CCAGTGGGACAGTAT | 996 |
rs764987612 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122924 | ATGATCCACCTGCCT[C/T]CCAAAGTGCTGGGAT | 996 |
rs765054496 | snp | C/T | 3.54491e-05 | 0.0042099 | intron-variant | CDC27 | GRCh38.p7 | 17:47142070 | AAAAAACGCAATAAA[C/T]TAGTCTGCTTCTCTA | 996 |
rs765173176 | snp | C/G | 1.73099e-05 | 0.00294188 | intron-variant | CDC27 | GRCh38.p7 | 17:47169879 | AAACATACTTGTATG[C/G]AAATGCTTTTCTGAC | 996 |
rs765179637 | in-del | -/TTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132741 | AGCCATTAAAGCAGT[-/TTA]TTATTATTATTATTA | 996 |
rs765222132 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160105 | TAATGAAAAGGAAAA[C/T]TTATGTTTCTTTCTA | 996 |
rs765240243 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176545 | GGCTCCTTAGTGTTT[C/G]AGGCAGAAAATGGCA | 996 |
rs765270243 | in-del | -/CAAG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175081 | AAGGAAGGAAGGAAG[-/CAAG]GAAGGAAGGAAGGAA | 996 |
rs765293554 | snp | A/G | 1.68119e-05 | 0.00289926 | intron-variant | CDC27 | GRCh38.p7 | 17:47132218 | AACATATTTCAAAAG[A/G]GAGATTAATAGAGTA | 996 |
rs765363744 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126350 | GCCTCATAATTCAGC[A/G]AAGCCCCAAGCTCAT | 996 |
rs765423924 | snp | A/G | 2.46996e-05 | 0.00351414 | intron-variant | CDC27 | GRCh38.p7 | 17:47154652 | ATCAATTCCCAAACT[A/G]CATTTTACATGGAAA | 996 |
rs765426042 | snp | A/G | 0.00138897 | 0.0263165 | stop-gained, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137327 | TATCATGTTCCCGTT[A/G]CAGACTGAAACAGTT | 996 |
rs765477385 | snp | A/T | 1.67424e-05 | 0.00289326 | synonymous-codon, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151934 | CTGTAAAACACGAAA[A/T]GTCTAAGGTTTGTGA | 996 |
rs765559479 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169096 | TCCTGGGCTCAAGAG[A/C]TCCTCCACCTCAGTC | 996 |
rs765575181 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165427 | TCCTTAATGGCTAAC[A/G]ATTTAGAACATCTTT | 996 |
rs765581281 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133993 | TGGCCTTAAGTGATC[G/T]GCTTGTCCCAGCCTA | 996 |
rs765637700 | snp | A/G | 5.18139e-05 | 0.00508962 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189223 | GGCCCCCCCTGTAGC[A/G]GCTCCGGCCCGGCCA | 996 |
rs765661411 | snp | A/C | 2.66003e-05 | 0.00364684 | intron-variant | CDC27 | GRCh38.p7 | 17:47137381 | AAAAATGGGAACAAA[A/C]ACCAAACAGAATTAA | 996 |
rs765666227 | in-del | -/CCTGAAA | 8.80693e-05 | 0.00663527 | intron-variant | CDC27 | GRCh38.p7 | 17:47157124 | TCAATCTGTTTAATT[-/CCTGAAA]CAGAAAATTTCTACC | 996 |
rs765679354 | snp | C/G | 1.69085e-05 | 0.00290757 | intron-variant | CDC27 | GRCh38.p7 | 17:47122403 | ATCCTTATGCAAAAG[C/G]TAACTTTCTAAATAC | 996 |
rs765689910 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170870 | TTGTGGGAGGCCAAG[A/G]TGGGAGGACAGCTTG | 996 |
rs765714462 | in-del | -/TTC | | | cds-indel, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118690 | CTTGATCAAAATGTG[-/TTC]TTCTTCGGGTTGTTT | 996 |
rs765735400 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161539 | GTGGATCACTTGAGG[A/T]CAGGAGTTCGAGACC | 996 |
rs765736331 | snp | C/T | 3.30327e-05 | 0.0040639 | missense, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122570 | AGAAATTCATCAGGG[C/T]GAGGTGCGTTTGACC | 996 |
rs765771425 | in-del | -/GTG | 6.65126e-05 | 0.00576644 | cds-indel, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141919 | CCAACCAGTATTGTA[-/GTG]GTGAGAAGGTAGATG | 996 |
rs765815446 | snp | C/T | 1.68732e-05 | 0.00290454 | intron-variant | CDC27 | GRCh38.p7 | 17:47157196 | TCTTTGTAGTTTTCA[C/T]AATATTTTGAACACT | 996 |
rs765851979 | in-del | -/A | 0.110707 | 0.207599 | intron-variant | CDC27 | GRCh38.p7 | 17:47157395 | TTCACCTGTGAAGAC[-/A]AAAAAAAAAAAAGTT | 996 |
rs765901724 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153382 | ACCTGGCATGCTAAC[C/T]ACCATTTTGTTTTGC | 996 |
rs765916650 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168830 | TTGAAAAATAACCAA[A/T]ATTCAAACTAGCCTC | 996 |
rs765919845 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137129 | TCAATACGACTTTGT[A/C]TTTGTACTTCATTAC | 996 |
rs765977984 | snp | G/T | 4.20353e-05 | 0.00458431 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142364 | GAGTTATTCCTCCTT[G/T]ATTAGTTTTACTTTT | 996 |
rs766008700 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176760 | GGTTAGATTTGAATA[C/T]ATTGAGTTTGATGTG | 996 |
rs766020946 | snp | G/T | 7.44241e-05 | 0.00609972 | intron-variant | CDC27 | GRCh38.p7 | 17:47154839 | CAAGGCATATATAAA[G/T]CAGCAGTATACTTAA | 996 |
rs766030918 | in-del | -/TTAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177780 | TTCCATAGGTAGCAA[-/TTAC]TTATGAAAAAAATGC | 996 |
rs766044928 | in-del | -/AAAATAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135977 | ATCCCGTCTCTACTA[-/AAAATAC]AAAATACAAAAAAAA | 996 |
rs766066060 | snp | A/T | 6.00528e-05 | 0.00547931 | intron-variant | CDC27 | GRCh38.p7 | 17:47132402 | AACAAAGTATAATTT[A/T]AAAAATATAAAGTTT | 996 |
rs766078229 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150992 | GGCCGAGATCACACC[A/G]CTGCACTCCAGCTTG | 996 |
rs766117351 | in-del | -/G | 0.001068 | 0.0230837 | intron-variant | CDC27 | GRCh38.p7 | 17:47154871 | TTAGAAGGTCTAAAA[-/G]GAAGAGAATGGCAAA | 996 |
rs766128843 | in-del | -/GA | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189406 | CCGAGGTTGGTCGAC[-/GA]GAGAGAGAAAACCGT | 996 |
rs766131376 | snp | C/T | 1.99651e-05 | 0.00315945 | intron-variant | CDC27 | GRCh38.p7 | 17:47181535 | GTTATTCATTTATCA[C/T]TCTACAGCAATGAAT | 996 |
rs766140161 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162204 | ACAGCCAATCAGCAA[C/T]GAAGCCATAATTCAT | 996 |
rs766153420 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178132 | AAACAGCAAATCTCA[A/G]CTCACTAGTGGACTG | 996 |
rs766176364 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138258 | ATGTTGACTACAGAA[C/T]TACCGCAAATAATGG | 996 |
rs766206603 | snp | C/T | 3.31686e-05 | 0.00407225 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156998 | CCTGTTTAGATAATA[C/T]GGAAGTTCCTGTTCC | 996 |
rs766211263 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122742 | GCAATGGCACGATCT[G/T]GGCTCACTGCAACCT | 996 |
rs766302829 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160002 | TGAAACCTCTGCTTC[-/T]TTTTTTTTTTTTTCA | 996 |
rs766303407 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120881 | TATACAGAGGGACAA[G/T]AAACACGTCAGCACT | 996 |
rs766304640 | snp | C/T | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117247 | TGAACCTTCATGAAC[C/T]ATAAGTTGTCAGCTA | 996 |
rs766312950 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131496 | CCATTCCCACAAAAG[C/T]TAAACTTGCTAGGGG | 996 |
rs766360844 | snp | C/T | 3.93345e-05 | 0.0044346 | intron-variant | CDC27 | GRCh38.p7 | 17:47156899 | CACATTTGAAAGTAT[C/T]TTGTTTGACTTACCT | 996 |
rs766385016 | snp | C/T | 3.40675e-05 | 0.00412705 | intron-variant | CDC27 | GRCh38.p7 | 17:47141844 | TATATAACCATTTTC[C/T]ATACTTACTTGCATG | 996 |
rs766435730 | snp | C/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190187 | GTGGTGGGAAGAGTA[C/G]GGGGTCGGAAATTCA | 996 |
rs766471439 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134087 | AATTTTTTGTGGAGA[C/T]GAGGTCTCACTATGT | 996 |
rs766541430 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174849 | TGATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA | 996 |
rs766545759 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156854 | CATTACTAACAATAT[A/G]AGTTATCATAAGATC | 996 |
rs766564213 | snp | C/G | 0.000100306 | 0.00708117 | intron-variant | CDC27 | GRCh38.p7 | 17:47158344 | ATAAGCTACAAACCC[C/G]AAAACCTGTATCATA | 996 |
rs766619286 | snp | C/T | 1.68471e-05 | 0.00290228 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47123906 | CTATTAAGAAGTAAA[C/T]GAGGGATTCTTTGGG | 996 |
rs766631334 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173512 | TTTCTTTTCACCTTA[C/T]AAGTTTTTAAAAACT | 996 |
rs766644276 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118727 | CCCATTCCATGCAAA[A/G]AACAAAACCAAACAA | 996 |
rs766672002 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159095 | TAATTCTGAAAGTGA[C/T]TTAAATGCTTTAAAT | 996 |
rs766697155 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183324 | TAAGTGATTAATATG[C/T]CTTAGATACAGTAAA | 996 |
rs766725312 | snp | A/G | 1.65075e-05 | 0.00287289 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129421 | TTTGCAAATAAAACT[A/G]AGGCTCTGTGAAATT | 996 |
rs766761853 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126237 | TGACCAGGGAATGAC[A/G]CAGCCCCAGGAGATC | 996 |
rs766784063 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143477 | ATAAAATTTTATCAC[A/G]TGAATGGATCTGTGT | 996 |
rs766821918 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184560 | CAAGGGCGGGGGGAA[A/G]AAAGAAGGAAAAAAG | 996 |
rs766831692 | snp | G/T | 1.66413e-05 | 0.0028845 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189128 | CAGCCAAGCCCCAGA[G/T]AAGAAGGTTATCATT | 996 |
rs766866034 | snp | A/C/G/T | 0.00106201 | 0.023025 | intron-variant | CDC27 | GRCh38.p7 | 17:47137377 | TTAAAAAAATGGGAA[A/C/G/T]AAAAACCAAACAGAA | 996 |
rs766898091 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188548 | CCTCCCCTGGTATTG[A/G]TGCTTGCGCCTCAGC | 996 |
rs766917735 | in-del | -/TGTC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47141616 | CACTCTACGTAAGAA[-/TGTC]TGGATGACTTGGGTC | 996 |
rs766956636 | in-del | -/GATAA | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189948 | AGAGAGGGCAATTGT[-/GATAA]GATAAGGAAAGTTCT | 996 |
rs767042213 | snp | C/G | 0.000179003 | 0.00945883 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142345 | CTATCATTTATGTTA[C/G]GTTGAGTTATTCCTC | 996 |
rs767060231 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182965 | CAGGAGTTCAAGGCT[A/G]TGATCATACCTGTGA | 996 |
rs767097480 | snp | C/T | 1.92073e-05 | 0.00309892 | intron-variant | CDC27 | GRCh38.p7 | 17:47157161 | AAGTCATTCACAATA[C/T]ATTATTTAGTTCAGA | 996 |
rs767099115 | snp | A/G | 1.66175e-05 | 0.00288244 | intron-variant | CDC27 | GRCh38.p7 | 17:47121069 | TGACAAATATGTCCT[A/G]TTGGTTCATGAAAAC | 996 |
rs767102148 | snp | A/T | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190422 | GGGGACTGTTTAAAT[A/T]TTGTTTTTCAGCAGA | 996 |
rs767179498 | snp | G/T | 2.54359e-05 | 0.00356613 | intron-variant | CDC27 | GRCh38.p7 | 17:47142210 | AATACAAAGATAATA[G/T]TAAGCATTTAAAACA | 996 |
rs767267065 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128771 | TTTTTTAATTTTTAA[-/T]TTTTTTTTTTTTTTT | 996 |
rs767298623 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180841 | ATATTAAAGTAACTC[A/G]TCCAAGGTTATAAAA | 996 |
rs767315582 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120605 | CACTATTTTCCATAT[-/C]TAATGGTTCCTTCAA | 996 |
rs767355429 | snp | A/C/T | 6.12043e-05 | 0.00553164 | intron-variant | CDC27 | GRCh38.p7 | 17:47132384 | CCATACCTGAAAGTA[A/C/T]AAAACAAAGTATAAT | 996 |
rs767417321 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138018 | TTGCCGAGGCTGGTC[G/T]TGGAACTCCTGAGCT | 996 |
rs767418800 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131094 | AGAGAAAAGCTTACT[C/T]TCTTACCTGACAATT | 996 |
rs767445175 | snp | C/T | 2.86874e-05 | 0.0037872 | intron-variant | CDC27 | GRCh38.p7 | 17:47137124 | CACCATCAATACGAC[C/T]TTGTCTTTGTACTTC | 996 |
rs767462500 | in-del | -/AGAA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175026 | GAAAGAAAGAAAGAG[-/AGAA]AGAGAGAGAGAGGAA | 996 |
rs767537719 | snp | A/C | 1.65468e-05 | 0.00287631 | intron-variant | CDC27 | GRCh38.p7 | 17:47154815 | GAAATCAAGGTGTCA[A/C]AAAGTCATCAAGGCA | 996 |
rs767542427 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120735 | TTCATACTGGTAAAA[A/G]AGCCAGTCTTGTTAG | 996 |
rs767576982 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187986 | AATTCAAACACTAAT[A/C]GCTGCTATATGTAAA | 996 |
rs767590855 | snp | A/G | 0.00583962 | 0.0537188 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47172003 | GAGTCTATATGCTTT[A/G]TATGCCTTTCCTGAG | 996 |
rs767647734 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128370 | CTTCATGGTTTCTGA[C/T]TGAATAAATGATAAC | 996 |
rs767667676 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184426 | AAAAGACTCAAATGA[A/T]TTACCAGCTATTTTA | 996 |
rs767684982 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188266 | TCCCAGACCTGGTCC[A/T]TTACCAAGGCACAAA | 996 |
rs767736866 | snp | C/G | 1.71452e-05 | 0.00292785 | intron-variant | CDC27 | GRCh38.p7 | 17:47123878 | GGGACCATGACCCCA[C/G]TCTTTACCTTTCCTA | 996 |
rs767759911 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158596 | AGATGTGAAAAACAT[C/G]CAAATCCTTCAGTAT | 996 |
rs767769578 | snp | A/C | 3.29614e-05 | 0.00405951 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157334 | GCAGACAGTTGCTAA[A/C]GTTCTGTAAAGATGT | 996 |
rs767773046 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187000 | CACTATCCCTGATCA[C/T]TGATCTTTATCATTG | 996 |
rs767793820 | snp | A/C/G | 3.41106e-05 | 0.00412969 | intron-variant | CDC27 | GRCh38.p7 | 17:47141836 | GAAAGGCATATATAA[A/C/G]CATTTTCTATACTTA | 996 |
rs767809570 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173403 | AATGGGGCGCTCACT[A/G]CAGTAGGAATAAACT | 996 |
rs767833169 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133948 | TAGAGACGAGGTTTC[C/T]CCATGTTGGCCAGGC | 996 |
rs767929626 | snp | C/G | 1.69922e-05 | 0.00291476 | intron-variant | CDC27 | GRCh38.p7 | 17:47151761 | AGAAATGTAAAGAAT[C/G]AAGTTTTATGCCAAG | 996 |
rs767937604 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156601 | TACAGGCGCCCGCCA[C/T]CATGCCCAGCTAATT | 996 |
rs767952055 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143256 | GGCGTGAGCCACTGC[A/G]TCCGCCGGGTCTCCA | 996 |
rs768033661 | snp | A/G | 1.65828e-05 | 0.00287943 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151916 | GCCGATTCTGGCAAC[A/G]GACTGTAAAACACGA | 996 |
rs768085792 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143167 | TGGGGTCTTGCTATG[A/T]TGACCAGGCTGGTCT | 996 |
rs768103993 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134871 | CTCAAGTAATCTTCC[A/T]GCTTCAGCTTCCTAA | 996 |
rs768104637 | snp | C/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137211 | ACAAGCTAATGCTTT[C/G]TCCAATTCTTCAGTT | 996 |
rs768141617 | in-del | -/TTTC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128029 | CACTGGTTTGGTATA[-/TTTC]TTTCTATTTTTCTTT | 996 |
rs768263500 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133384 | CTCAGGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 996 |
rs768301440 | snp | A/G | 1.66499e-05 | 0.00288525 | intron-variant | CDC27 | GRCh38.p7 | 17:47138718 | GGTAACTATATAAGC[A/G]AAGTATTTTGGTTAA | 996 |
rs768351953 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176687 | AACATAAATTTGGGA[A/G]GGGAAAAGGAACAGG | 996 |
rs768353617 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144794 | TTCAGAAAATAAAAA[G/T]ATATATATTTTCATC | 996 |
rs768372223 | snp | A/G | 3.30475e-05 | 0.00406481 | intron-variant | CDC27 | GRCh38.p7 | 17:47121043 | AAAACAGAAGTCCAC[A/G]GTAAGTTTTCTGACA | 996 |
rs768386741 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182664 | ATTCATTCTTGATGT[G/T]TGTAGCTAGAGTTCA | 996 |
rs768434424 | in-del | -/C | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189418 | CGACGAGAGAGAAAA[-/C]CGTTGCCGGAAATTG | 996 |
rs768494356 | in-del | -/TCT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124710 | AGATTCTCACATCTA[-/TCT]TCTGCTTCTCCATTT | 996 |
rs768494724 | snp | A/G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130960 | ACAAATATCATGGTC[A/G/T]TAAGAATGTGAGAAT | 996 |
rs768524392 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153112 | GGACAAAAGTCAACT[A/C]TGGCTTTTCCTTATT | 996 |
rs768537699 | snp | C/T | 1.80393e-05 | 0.00300322 | intron-variant | CDC27 | GRCh38.p7 | 17:47143840 | AGAAATGTTAGCAGG[C/T]GAAGCATTAAGTAAA | 996 |
rs768584652 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184279 | AGTATACTATCATAC[A/G]TTAAGCACTTGGAAA | 996 |
rs768608998 | snp | C/G | 1.65181e-05 | 0.00287381 | missense, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122459 | TGATCTGTTCTTCTT[C/G]GGTTATTGGCTCCTC | 996 |
rs768610426 | snp | A/C/T | 0.00140539 | 0.0264715 | stop-gained, missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137152 | TTCATTACCACTTAC[A/C/T]ATGCATTATAATGTC | 996 |
rs768630985 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145101 | CATGACAGAGTAAAA[G/T]GGAATAAATTTATTC | 996 |
rs768653388 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47122086 | CAAGTTTTCTGGAAC[A/C]AAGGCATCTAATCAG | 996 |
rs768777498 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163762 | GTCTCATAAGATTAT[C/T]TGTTTCTTTTGCTTT | 996 |
rs768837458 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133895 | CTGGGATTACAGGCA[A/T]GTGTCACCACGCCCA | 996 |
rs768888967 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140688 | AGAAATAATTTTTTA[A/T]ATGGCTTTTCCGAAC | 996 |
rs768902228 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169696 | ACCTAACATGTATGA[C/T]CAATTGTTAGGCAGG | 996 |
rs768905994 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165142 | CTATCTAAGTTACTA[G/T]ACATATCAATATAGT | 996 |
rs768906900 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188102 | TAAAATATTTACTGT[C/T]TGATACCTCAAGCCT | 996 |
rs768925314 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149426 | TGAGGCAGGAGAATC[A/G]CTTTAACCCAGGTGG | 996 |
rs768964687 | snp | C/T | 5.26745e-05 | 0.00513171 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181592 | GTTCTGCGAGGAAAA[C/T]CGCATCTCGGTAAGC | 996 |
rs769017825 | snp | C/T | 0.000111757 | 0.00747435 | intron-variant | CDC27 | GRCh38.p7 | 17:47172114 | CAGTATATTGAATGA[C/T]AATCAGTTTATCATG | 996 |
rs769053380 | snp | A/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189943 | AATTCAGAGAGGGCA[A/G]TTGTGATAAGATAAG | 996 |
rs769120753 | snp | A/G | 8.31e-05 | 0.00644539 | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156959 | CTCCTAATAAACTTC[A/G]ACCAGTTTTTGGTTT | 996 |
rs769186427 | snp | G/T | 3.48299e-05 | 0.00417297 | intron-variant | CDC27 | GRCh38.p7 | 17:47157388 | CTGGCTTTTCACCTG[G/T]GAAGACAAAAAAAAA | 996 |
rs769205135 | snp | A/C | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189630 | CAGTGTGGATTAGCC[A/C]CTCAGCCCTTTTGGA | 996 |
rs769232526 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150040 | ACAATAATGCACTGT[-/G]GGGTTTATAACATAT | 996 |
rs769258407 | snp | C/T | 1.76291e-05 | 0.00296888 | intron-variant | CDC27 | GRCh38.p7 | 17:47158307 | CGATCTGTCTTGCTG[C/T]GGAGAGAAACAAGTA | 996 |
rs769264253 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135208 | TATAGCATACATAGT[A/G]TCATGTTTGGCTTCC | 996 |
rs769286069 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156283 | AGCTGGATCTACAGG[C/T]GCGTGCCACCACACC | 996 |
rs769305277 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156502 | GCCCAGGATGGAGTG[C/T]AGTGGCTCCATCTCG | 996 |
rs769310078 | in-del | -/A | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157040 | ATCAGGTGAAATTAC[-/A]AGCTGAATCAATATA | 996 |
rs769310729 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172593 | GATAAATTATAAATT[A/G]TGAATGCTCACACCA | 996 |
rs769332991 | snp | A/G | 1.66882e-05 | 0.00288857 | intron-variant | CDC27 | GRCh38.p7 | 17:47129535 | ACCTGTAAGAAATAA[A/G]GATCATGTTAATACT | 996 |
rs769356150 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132724 | GCATGAACCACAATG[C/T]CTAGCCATTAAAGCA | 996 |
rs769417704 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144430 | TTTTACCCTTCATTT[A/G]CAACTACAACAAGTT | 996 |
rs769470978 | snp | A/T | 1.96547e-05 | 0.0031348 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47121013 | CTGGGATTCATCTGT[A/T]CCCACTTTAAAAATA | 996 |
rs769516966 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182697 | TGTTTTCATTGCTGA[A/G]TAAATAATATTTCCA | 996 |
rs769532884 | snp | C/T | 0.00307909 | 0.0391161 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137280 | GTAATTTGGATCAAC[C/T]TGGATAGCTCTCTGG | 996 |
rs769552755 | in-del | -/G | 2.77735e-05 | 0.00372639 | intron-variant | CDC27 | GRCh38.p7 | 17:47154632 | AAATAAACAAGTTGC[-/G]TTTAATCAATTCCCA | 996 |
rs769586419 | snp | C/T | 9.91359e-05 | 0.00703975 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151903 | TTGTTCCAGTTTGGC[C/T]GATTCTGGCAACAGA | 996 |
rs769663726 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166912 | CAGGTTGGAGTGCAA[C/T]GGTGTGATCTCGACT | 996 |
rs769683847 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126765 | AGTTAAAAGTTGAAA[C/T]GGGCTTATTAGATTT | 996 |
rs769689952 | snp | C/G | 0.00247362 | 0.0350812 | intron-variant | CDC27 | GRCh38.p7 | 17:47157131 | GTTTAATTCCTGAAA[C/G]AGAAAATTTCTACCA | 996 |
rs769701199 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182534 | TTTATACATTTGTAC[A/C]TATCATCTCTAAGCA | 996 |
rs769748660 | snp | A/G | 1.66582e-05 | 0.00288597 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157074 | CACTGAGGAATCTGT[A/G]TTCAAGGAGTACTTT | 996 |
rs769759034 | snp | A/C | 0.000513567 | 0.0160162 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137348 | TGAAACAGTTCCCTG[A/C]AGCACACCAGGCCTT | 996 |
rs769787259 | in-del | -/AA | 0.0025802 | 0.0358252 | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47157126 | ATCTGTTTAATTCCT[-/AA]GAAACAGAAAATTTC | 996 |
rs769795074 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137722 | TTTGGCTCTGGGGAC[A/C]GTTGGACAGAATTTG | 996 |
rs769803542 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120468 | TCTTTTATTGTTCCA[C/T]CTGGCACTTGCAAAC | 996 |
rs769908788 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177776 | AGAGTTCCATAGGTA[A/G]CAATTACTTATGAAA | 996 |
rs769911233 | snp | C/T | 0.00014694 | 0.0085702 | intron-variant | CDC27 | GRCh38.p7 | 17:47142457 | AAAGGGAAGAAATTT[C/T]ACACCTGTTATACTC | 996 |
rs769974922 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123350 | TCTCAGAAGCCATTT[C/G]TCTTAATCAAGACAA | 996 |
rs769976240 | snp | C/T | 2.0415e-05 | 0.00319486 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142311 | AATGATGGAAGAGTC[C/T]AATTTTGTAATTTCC | 996 |
rs770038377 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47154088 | AGCGAGACCCTGTCT[-/C]AAAAAAAAAAAAAAA | 996 |
rs770052635 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139742 | ATATACACACCAATA[C/T]TGTGTCTGCTAGGAA | 996 |
rs770060146 | snp | A/G | 1.65693e-05 | 0.00287826 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132337 | TTTCTGCAAGGCTGA[A/G]TTTTTCTTGCTTGTA | 996 |
rs770063769 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124858 | CTCTAGGACTCCTTG[A/G]AAGGATTTTAGGGAC | 996 |
rs770065515 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121599 | AGACACGTACCACCA[C/T]AGCCAGCTACTTTTA | 996 |
rs770073775 | in-del | -/T | 1.69085e-05 | 0.00290757 | intron-variant | CDC27 | GRCh38.p7 | 17:47122403 | TCCTTATGCAAAAGG[-/T]TAACTTTCTAAATAC | 996 |
rs770151870 | in-del | -/AG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175030 | GAAAGAAAGAGAGAA[-/AG]AGAGAGAGAGGAAGG | 996 |
rs770152345 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121940 | AGACGAGGTTTCACC[A/G]TGTTGGTCAGCTGGT | 996 |
rs770215962 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148055 | ATACAAAAATTAGCA[C/G]GGCGCAGTGGCACAT | 996 |
rs770247096 | snp | A/G | 1.70577e-05 | 0.00292037 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138869 | TTCTCAATCCTTCTA[A/G]CCTCTGAGAATATTC | 996 |
rs770264389 | snp | C/T | 0.000201969 | 0.0100471 | intron-variant | CDC27 | GRCh38.p7 | 17:47172106 | CTATTGTTCAGTATA[C/T]TGAATGATAATCAGT | 996 |
rs770286521 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130307 | AGAGGTTGCAGTGAG[C/T]CAAGATCGCGCCACT | 996 |
rs770297539 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187776 | TAAATAACTTGAGTA[A/T]TCTGCTTATCTATTT | 996 |
rs770302536 | snp | A/T | 0.00136964 | 0.0261332 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138749 | CATACCTCTGGCGAA[A/T]TTTTATCCATGTCTG | 996 |
rs770306644 | in-del | -/ACAGG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174973 | GACTATCGAAACAGG[-/ACAGG]ACAGGACAGGACAGG | 996 |
rs770331276 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170640 | TATGTACAAATCCAG[C/T]CTGAGCAACATATTC | 996 |
rs770352273 | snp | A/C | 2.1453e-05 | 0.00327506 | intron-variant | CDC27 | GRCh38.p7 | 17:47156864 | AATATGAGTTATCAT[A/C]AGATCATTTGGTATT | 996 |
rs770383894 | in-del | -/C | 5.13822e-05 | 0.00506838 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189210 | CTGCAGTGCCTCAGG[-/C]CCCCCCTGTAGCGGC | 996 |
rs770393628 | snp | A/C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133851 | CCTCCTGGGTTCAAG[A/C/T]GATTTTCGTGCCTCA | 996 |
rs770410921 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187593 | AGGTGTAAGCCACCA[C/T]GCCCGGCCTTCCATG | 996 |
rs770427320 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186093 | CAGTTGGATTATTCT[A/G]CTAGTCTGTATGTCT | 996 |
rs770427639 | in-del | -/CCTGGGG | 1.70936e-05 | 0.00292344 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157238 | CACTTACAATTGTGT[-/CCTGGGG]TGTTTCCGTAAGAAC | 996 |
rs770480011 | snp | C/T | 0.00014927 | 0.00863786 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141931 | GTAGTGGTGAGAAGG[C/T]AGATGGCTCAAAATA | 996 |
rs770507862 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128426 | TATCTCTTTCTCAGT[G/T]TCCTTATCTTCTTTT | 996 |
rs770531935 | snp | A/T | 0.000168867 | 0.00918721 | intron-variant | CDC27 | GRCh38.p7 | 17:47154622 | TTAAAAGATTGAAAT[A/T]AACAAGTTGCTTTAA | 996 |
rs770622202 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159793 | CCCCAGGAAAAAGTC[A/G]ATGATCTCAGATTCC | 996 |
rs770624940 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127743 | GGTCTAGCTTTGTGG[C/T]CCAGGCTGAAGTGCA | 996 |
rs770652924 | snp | A/G | 0.0001092 | 0.00738838 | intron-variant | CDC27 | GRCh38.p7 | 17:47172113 | TCAGTATATTGAATG[A/G]TAATCAGTTTATCAT | 996 |
rs770679862 | snp | A/C/T | 3.42016e-05 | 0.0041352 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158292 | GATCCTTTGGCAAGC[A/C/T]GATCTGTCTTGCTGT | 996 |
rs770733960 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180813 | TTTATAGATGAAATA[C/T]CTGAATTTTCAGATA | 996 |
rs770785814 | in-del | -/T | 0.00710834 | 0.0591916 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47170023 | CTCCACCAGATAAGA[-/T]TTGTTCCCCTTCTGC | 996 |
rs770786086 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140746 | TACATACCAGTAAAG[C/G]ACCATAATCGAAACA | 996 |
rs770820672 | snp | G/T | 0.0179479 | 0.0930151 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137170 | GCATTATAATGTCTA[G/T]GATTGACTCTGATAG | 996 |
rs770879848 | snp | C/G | 1.7141e-05 | 0.0029275 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189210 | CTGCAGTGCCTCAGG[C/G]CCCCCCTGTAGCGGC | 996 |
rs770934538 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151505 | TGTGGGGAAGGGGAG[A/T]ATGAAACCTATCTGT | 996 |
rs770958176 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125449 | ACGCGGTTTCACCAT[A/T]TTGGCCAGCTGGTCT | 996 |
rs771047738 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142768 | AACCCAACCTCTGCC[A/T]CCCGGGTTCAAGCGA | 996 |
rs771051841 | snp | A/T | 0.000250428 | 0.0111871 | intron-variant | CDC27 | GRCh38.p7 | 17:47124003 | GTAGCAAAAATTTTT[A/T]AAGTTTTGACCAAGC | 996 |
rs771069720 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168074 | TGCCAGGAACCTCCA[C/T]GTGTTCAGTTTTCTG | 996 |
rs771084076 | snp | C/T | 1.82623e-05 | 0.00302173 | missense, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120981 | TGTGTGTCATCCGCA[C/T]CTGTCATGCTGCTCT | 996 |
rs771110019 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120094 | TCTGATTCATATGGT[C/G]AACTTAAGGGGTTAT | 996 |
rs771111007 | snp | G/T | 0.000266618 | 0.0115429 | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157063 | TCAATATAAGACACT[G/T]AGGAATCTGTATTCA | 996 |
rs771199389 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164896 | TTTACACGTTTATAT[A/G]GAGAATATTATCACA | 996 |
rs771240299 | snp | C/T | 1.69559e-05 | 0.00291164 | intron-variant | CDC27 | GRCh38.p7 | 17:47129566 | CCCTCTTGATATTTA[C/T]GAAGAAAGGTGAGAA | 996 |
rs771281232 | in-del | -/GAAGGAAGGA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175042 | GAAAGAGAGAGAGAG[-/GAAGGAAGGA]AGGAAGGAAGGAAGG | 996 |
rs771307719 | snp | A/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190160 | TATTTTTGATAGGTG[A/G]GGCATTCCGCTGTGG | 996 |
rs771334710 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165232 | CTGAATTTTGGGTTG[-/T]TTTCCAGTTTTGGGC | 996 |
rs771350489 | in-del | -/CA | 6.88901e-05 | 0.00586859 | intron-variant | CDC27 | GRCh38.p7 | 17:47123876 | TTGGGACCATGACCC[-/CA]GTCTTTACCTTTCCT | 996 |
rs771352776 | snp | C/T | 3.29777e-05 | 0.00406051 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169994 | ATCATCATGGCTTTT[C/T]TGCTTATTAAACACT | 996 |
rs771367384 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145045 | ATTCTAATCATCTCT[-/A]AAAAAAACTTTCTAA | 996 |
rs771398215 | snp | A/G | 1.7144e-05 | 0.00292775 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154729 | AGGTGTATTAGTGTA[A/G]TTTTGTAAATAGGAT | 996 |
rs771413780 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161672 | GGAGAACTGCTTGCA[A/T]CCTGGAGGTGGAGGT | 996 |
rs771438943 | snp | C/T | 2.72009e-05 | 0.00368778 | intron-variant | CDC27 | GRCh38.p7 | 17:47154638 | AACAAGTTGCTTTAA[C/T]CAATTCCCAAACTGC | 996 |
rs771471986 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184398 | ACTGCTTATTTTGCA[A/G]TATATAAGCCACAAA | 996 |
rs771482281 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162535 | GAATGTGATATAAAA[-/C]AGACATTTTTATTAA | 996 |
rs771502641 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161430 | GGCAAATCAGTGCTT[A/G]GGAGCTTTTAACATA | 996 |
rs771584304 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168495 | ACCTTTGAGGGTGGG[A/G]ACTGTGAGTTATTTA | 996 |
rs771589140 | in-del | -/A/AA | 0.0018048 | 0.0299915 | intron-variant | CDC27 | GRCh38.p7 | 17:47157392 | TTTTCACCTGTGAAG[-/A/AA]ACAAAAAAAAAAAAA | 996 |
rs771618415 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162905 | ATATGTATAAATCAC[A/C]TAAGAGCTAACTAGG | 996 |
rs771631452 | snp | C/T | 1.65018e-05 | 0.00287239 | synonymous-codon, missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122469 | TTCTTGGGTTATTGG[C/T]TCCTCATCATCTGGA | 996 |
rs771634312 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144996 | GCAAATGACACACAA[C/T]CTTTCTTGGATGATT | 996 |
rs771690668 | in-del | -/CTCAGGCCCACTTTCTGCAGTGC | 1.67242e-05 | 0.00289168 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189181 | CCGTCATCCTCGAGG[-/CTCAGGCCCACTTTCTGCAGTGC]CTCAGGCCCCCCCTG | 996 |
rs771713917 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185514 | TTTTTGTTAGAGAAA[C/G]CTTATTACAAAAAAT | 996 |
rs771765235 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150789 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 996 |
rs771774043 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128337 | CGCCCAGCCCTGAAT[G/T]TATTTTAAAAGATTT | 996 |
rs771819554 | snp | A/G | 8.24355e-05 | 0.00641957 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157360 | GATGTGAATTTAAAT[A/G]TTTGGTCAGGATCTG | 996 |
rs771905598 | snp | A/C | 1.88645e-05 | 0.00307114 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143969 | TAGTGGGGCTCAATA[A/C]CTGAGGTGTTGTACT | 996 |
rs771913166 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135056 | TTCGAATAAGGAAAC[C/T]GAAACTTAGAGAAGT | 996 |
rs771914033 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170466 | TGGGATCACAAGCAT[C/G]AGACACTGCACCTGG | 996 |
rs771959054 | snp | A/G | 5.31769e-05 | 0.00515612 | intron-variant | CDC27 | GRCh38.p7 | 17:47143855 | CGAAGCATTAAGTAA[A/G]TGTGACATACAGAAA | 996 |
rs771983482 | in-del | -/AG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131519 | GCTAGGGGGAAAAAA[-/AG]AGAGAAGCTGAGGGG | 996 |
rs771990014 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47154413 | ATTATGTTTATTTAA[C/T]TATATGCTGAAATAA | 996 |
rs772069803 | in-del | -/A | 6.71254e-05 | 0.00579294 | intron-variant | CDC27 | GRCh38.p7 | 17:47132227 | AAAAGGGAGATTAAT[-/A]AGAGTATTAATGTTT | 996 |
rs772135963 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149682 | AATTTCAGCTGGGCA[C/T]GGTAGCTCATGCCTG | 996 |
rs772151969 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165385 | TTATTTTTAGCCATT[A/G]TATCTAATGGTGGTT | 996 |
rs772153145 | snp | A/G | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117292 | TAGCTCCATGTCTAA[A/G]CTGCTGTTTATCCTT | 996 |
rs772186610 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139208 | TCAAAAGAAAAGTCA[A/G]TATTTCCTTCTCAAA | 996 |
rs772202286 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182294 | ATATGTTTTCTCTTT[C/T]AGAATTACAAAACAT | 996 |
rs772259400 | snp | C/T | 1.87883e-05 | 0.00306493 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181622 | CATAGTGGTTTAGTG[C/T]TTGCCATATAGCAGC | 996 |
rs772356719 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170488 | TGCACCTGGCCAATT[A/T]GTTTTTTGTAAAAAA | 996 |
rs772357299 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135384 | GATGGTTTATATTAC[A/G]GAGACTTCTCATGGC | 996 |
rs772370300 | snp | A/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190009 | GAGTTTGAAGGATGG[A/G]TAAAATTAGAGGAAA | 996 |
rs772425346 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137582 | TTGCAGTGCTTTCAT[A/C]GTCATCAAAAGGTAT | 996 |
rs772436784 | snp | C/T | 0.0331441 | 0.124393 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156984 | TGGTTTATTTTGAAC[C/T]TGTTTAGATAATATG | 996 |
rs772475829 | snp | C/T | 1.67281e-05 | 0.00289202 | intron-variant | CDC27 | GRCh38.p7 | 17:47129543 | GAAATAAAGATCATG[C/T]TAATACTCCCTCTTG | 996 |
rs772550581 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175731 | AGAGGTACAAGAATC[G/T]CTTGAACCTGGGAGG | 996 |
rs772569183 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174691 | AAAAAACAAACAAAT[C/T]AAGCCTGTAATCCCA | 996 |
rs772610316 | snp | A/G | 1.74248e-05 | 0.00295163 | intron-variant | CDC27 | GRCh38.p7 | 17:47142054 | ACATAGTAAACAAAG[A/G]AAAAAACGCAATAAA | 996 |
rs772653494 | snp | C/G | 1.90936e-05 | 0.00308973 | intron-variant | CDC27 | GRCh38.p7 | 17:47158334 | AGTAGATTAAATAAG[C/G]TACAAACCCCAAAAC | 996 |
rs772676113 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159743 | GTCTGCTTCTGCACC[A/G]GCATAATCTTCAAAA | 996 |
rs772723161 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon, missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122523 | TTTAATCTGGTTATT[A/G]GCTCCTTTAGGATCT | 996 |
rs772734148 | snp | C/T | 7.02309e-05 | 0.00592541 | intron-variant | CDC27 | GRCh38.p7 | 17:47143863 | TAAGTAAATGTGACA[C/T]ACAGAAATCTTTAAA | 996 |
rs772737513 | snp | A/G | 1.68903e-05 | 0.00290601 | intron-variant | CDC27 | GRCh38.p7 | 17:47157186 | TTCAGATCATTCTTT[A/G]TAGTTTTCATAATAT | 996 |
rs772760925 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185563 | TAAATTTTTTATACA[C/T]TTTGTGTTCTTGTTT | 996 |
rs772776521 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127415 | CTATTTTTACGTTTT[G/T]TTTTGAGATGGAGTT | 996 |
rs772789212 | snp | A/G | 1.64901e-05 | 0.00287137 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157277 | TCTCAGGCTGTCTGT[A/G]AGATAAACTATGATT | 996 |
rs772816976 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184469 | ACTAGGAAAATTTCA[C/T]ACACATATACTAAAG | 996 |
rs772847795 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145913 | AAAAAAAAAAAAGTC[A/G]ACCATGTGATTAGAG | 996 |
rs772870746 | in-del | -/TG | 2.29171e-05 | 0.00338497 | intron-variant | CDC27 | GRCh38.p7 | 17:47138943 | TACAATTTATATATA[-/TG]TACACAGGGAAAGCC | 996 |
rs772896202 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125409 | GTGCCACCATGCCTG[A/G]CTAATTTTTGTATTT | 996 |
rs772930848 | snp | C/G | 0.0161185 | 0.0883145 | intron-variant | CDC27 | GRCh38.p7 | 17:47137127 | CATCAATACGACTTT[C/G]TCTTTGTACTTCATT | 996 |
rs773011158 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148318 | GTGTGGTTAATAACA[C/G]GTCTGACACTGCTGA | 996 |
rs773012442 | snp | C/T | 1.91027e-05 | 0.00309047 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143970 | AGTGGGGCTCAATAC[C/T]TGAGGTGTTGTACTA | 996 |
rs773027111 | in-del | -/AAT | 1.64887e-05 | 0.00287125 | intron-variant | CDC27 | GRCh38.p7 | 17:47154802 | CTGAGAAGAGGTTGA[-/AAT]CAAGGTGTCAAAAAG | 996 |
rs773036216 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164814 | AGAGCGCAAGATTCC[A/G]TTTCAAACAACAACA | 996 |
rs773168963 | snp | A/G | 1.98041e-05 | 0.00314669 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181633 | AGTGCTTGCCATATA[A/G]CAGCCTGCAAATGGA | 996 |
rs773176432 | snp | A/T | 0.415261 | 0.187587 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137162 | CTTACCATGCATTAT[A/T]ATGTCTAGGATTGAC | 996 |
rs773201246 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138118 | ATTCTCTCTTTTGTA[A/T]AGAAAATAGGATCTA | 996 |
rs773219988 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166767 | CAACATCATAGTTTT[C/T]AATATGTCATATTTA | 996 |
rs773249675 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151325 | TCACAGTTTTAGAAA[A/G]GAGAAAGAAAATTGT | 996 |
rs773342094 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149715 | ATCCCAGCACTTTGG[A/G]AGGCTGAGGCGGGTG | 996 |
rs773363849 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173691 | TTGTGTGTACATGTG[-/C]CGTGTGTAATTTTAG | 996 |
rs773375395 | snp | C/T | 0.000149981 | 0.00865841 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156993 | TTGAACCTGTTTAGA[C/T]AATATGGAAGTTCCT | 996 |
rs773385822 | in-del | -/TAC | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117452 | AACCCTTCAGCTCTT[-/TAC]TGTACTTTCTCCAAG | 996 |
rs773435097 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119938 | AACCACACATTCTTA[C/T]ACTCTGCTTAAGCAA | 996 |
rs773466519 | snp | A/T | 6.60971e-05 | 0.00574841 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129408 | CTTATATTTTTCATT[A/T]GCAAATAAAACTGAG | 996 |
rs773522254 | snp | C/T | 1.90685e-05 | 0.0030877 | intron-variant | CDC27 | GRCh38.p7 | 17:47158335 | GTAGATTAAATAAGC[C/T]ACAAACCCCAAAACC | 996 |
rs773535490 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145242 | AAAAAGAATGCAAAA[C/T]AGAGCTCAGTGGTCC | 996 |
rs773553172 | snp | A/G | 1.74366e-05 | 0.00295263 | intron-variant | CDC27 | GRCh38.p7 | 17:47142056 | ATAGTAAACAAAGGA[A/G]AAAACGCAATAAACT | 996 |
rs773561651 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174810 | AAAATACAAAAATCA[G/T]CCGGGTGTGGTGGCG | 996 |
rs773586774 | snp | A/T | 1.65151e-05 | 0.00287355 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137310 | GAAGAATTTAATTGC[A/T]ATATCATGTTCCCGT | 996 |
rs773588814 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183015 | AGGAGCAAGACTCCC[A/T]TCAAAAAAACACAAA | 996 |
rs773606335 | snp | A/G | 1.66571e-05 | 0.00288587 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141973 | TTTGCAGTTGTATGA[A/G]CACAAAGCTAAATAA | 996 |
rs773632212 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118590 | TGCACCAACCTAATA[C/T]ATGTGTGAAACAGAG | 996 |
rs773637620 | snp | A/G | 1.66222e-05 | 0.00288285 | stop-gained, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151921 | TTCTGGCAACAGACT[A/G]TAAAACACGAAAAGT | 996 |
rs773676972 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158729 | GCTAAAGCCATCCTC[C/T]TACCTCAGCCTCCTG | 996 |
rs773680803 | in-del | -/AA | 2.19161e-05 | 0.00331022 | intron-variant | CDC27 | GRCh38.p7 | 17:47154884 | AAGGAAGAGAATGGC[-/AA]ATCAGTCTTAGGGAC | 996 |
rs773759852 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175767 | GTTGCAGTAAGCTGA[A/G]ATCACGCCACTGCAC | 996 |
rs773764699 | snp | A/C | 2.80761e-05 | 0.00374663 | intron-variant | CDC27 | GRCh38.p7 | 17:47154623 | TAAAAGATTGAAATA[A/C]ACAAGTTGCTTTAAT | 996 |
rs773765470 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170656 | CTGAGCAACATATTC[A/T]TTACTCATGTCAGAA | 996 |
rs773822435 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144806 | AAAGATATATATTTT[C/T]ATCTTTTACGATATG | 996 |
rs773826761 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125997 | TATCCCCACCCCCAG[C/T]GATCTAATTACAAGG | 996 |
rs773903629 | snp | A/G | 1.66402e-05 | 0.00288441 | intron-variant | CDC27 | GRCh38.p7 | 17:47138721 | AACTATATAAGCAAA[A/G]TATTTTGGTTAACAT | 996 |
rs773916575 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143207 | AAGCTCAAGTGATCG[A/G]CCCACCTTGGCCTCC | 996 |
rs774017692 | snp | A/T | 1.79906e-05 | 0.00299916 | intron-variant | CDC27 | GRCh38.p7 | 17:47157159 | CCAAGTCATTCACAA[A/T]ATATTATTTAGTTCA | 996 |
rs774081992 | snp | C/T | 0.00168139 | 0.0289459 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142337 | TTTCCAGGCTATCAT[C/T]TATGTTAGGTTGAGT | 996 |
rs774082297 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167063 | TTTCACCATGTTGGC[C/T]TGGCTGGTCTCAAAT | 996 |
rs774087111 | in-del | -/A/AA | 0.000269192 | 0.0115988 | intron-variant | CDC27 | GRCh38.p7 | 17:47157389 | GGCTTTTCACCTGTG[-/A/AA]AAGACAAAAAAAAAA | 996 |
rs774120940 | snp | A/G | 1.65138e-05 | 0.00287343 | missense, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122461 | ATCTGTTCTTCTTGG[A/G]TTATTGGCTCCTCAT | 996 |
rs774124933 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131012 | GCTAAACTCATCTAC[A/G]CAATGATCTAATGGT | 996 |
rs774144042 | snp | A/C | 0.0103888 | 0.0714352 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157259 | GTGTTTCCGTAAGAA[A/C]TGTCTCAGGCTGTCT | 996 |
rs774174424 | snp | C/T | 3.32939e-05 | 0.00407993 | intron-variant | CDC27 | GRCh38.p7 | 17:47121054 | CCACAGTAAGTTTTC[C/T]GACAAATATGTCCTG | 996 |
rs774256441 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153114 | ACAAAAGTCAACTCT[A/G]GCTTTTCCTTATTTA | 996 |
rs774265234 | in-del | -/AAGGAAGGAAGGAAGGAAGT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175079 | AGGAAGGAAGGAAGG[-/AAGGAAGGAAGGAAGGAAGT]AAGTTGTAGCAGCAC | 996 |
rs774294649 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137963 | CAGCCACCATACCTG[C/G]CTAATTTTTGTATTT | 996 |
rs774310725 | snp | A/C/T | 5.74293e-05 | 0.00535835 | intron-variant | CDC27 | GRCh38.p7 | 17:47132382 | AACCATACCTGAAAG[A/C/T]ATAAAACAAAGTATA | 996 |
rs774312667 | snp | A/G | 5.38895e-05 | 0.00519055 | intron-variant | CDC27 | GRCh38.p7 | 17:47143841 | GAAATGTTAGCAGGC[A/G]AAGCATTAAGTAAAT | 996 |
rs774333766 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118350 | AAAATGTAGGGACCA[-/C]CTTTCATTCTTTTGA | 996 |
rs774336770 | in-del | -/CACACACC/CACACC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124209 | ACACACACACACACA[-/CACACACC/CACACC]CCCCTCTTCGTGAAA | 996 |
rs774344431 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47152187 | ACTAAAAATCCCCAG[A/G]AGCTATTCTTTTCAT | 996 |
rs774346446 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168239 | CCTCCTGGGAGGTTG[C/T]GGGGTGGGGATGAAA | 996 |
rs774425267 | in-del | -/AAGGAAGGAAGGAAGT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175082 | AGGAAGGAAGGAAGG[-/AAGGAAGGAAGGAAGT]AAGGAAGGAAGGAAG | 996 |
rs774463382 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163828 | GGAGTACAATGGCAC[A/G]ATCTCAGCTCACTGC | 996 |
rs774469911 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47148355 | ATTAATTTGAAGACA[C/T]AGCAATAAACACTAT | 996 |
rs774491259 | in-del | -/AGGA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175044 | AAGAGAGAGAGAGGA[-/AGGA]AGGAAGGAAGGAAGG | 996 |
rs774510259 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169845 | TAAACACTGATCAAC[A/T]TAGGTTTTTTAAACT | 996 |
rs774562937 | in-del | -/AAATTTTT | 0.000817669 | 0.0202031 | intron-variant | CDC27 | GRCh38.p7 | 17:47123995 | ACCTTAAAGTAGCAA[-/AAATTTTT]AAAGTTTTGACCAAG | 996 |
rs774748215 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167509 | AGTTTTTCCTAGTTA[G/T]CACAACCCCTCTTCT | 996 |
rs774750632 | snp | A/C | 1.66729e-05 | 0.00288724 | intron-variant | CDC27 | GRCh38.p7 | 17:47129372 | ATACAACACTGAAGA[A/C]CCTTAAGATATTTAT | 996 |
rs774761256 | snp | C/G | 2.1381e-05 | 0.00326956 | intron-variant | CDC27 | GRCh38.p7 | 17:47156874 | ATCATAAGATCATTT[C/G]GTATTATAGCACATT | 996 |
rs774783141 | snp | A/G | 0.000903101 | 0.0212305 | intron-variant | CDC27 | GRCh38.p7 | 17:47157392 | CTTTTCACCTGTGAA[A/G]ACAAAAAAAAAAAAA | 996 |
rs774829802 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172910 | ACCAGTGAGCTGAAG[G/T]ATCTTCTAAGCCAGT | 996 |
rs774947895 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158430 | GTGATGCTTCTCTAA[G/T]TTACCAATTTCTCCC | 996 |
rs774955218 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143071 | TGACCTCCCCAGGCT[C/G]AAGTGATTCTCCCAC | 996 |
rs775004472 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127636 | TCAAACTCCTGACCT[C/T]GTGATCTGCCCGCCC | 996 |
rs775066848 | snp | G/T | 1.80059e-05 | 0.00300043 | intron-variant | CDC27 | GRCh38.p7 | 17:47158313 | GTCTTGCTGTGGAGA[G/T]AAACAAGTAGATTAA | 996 |
rs775080482 | in-del | -/G | 1.67335e-05 | 0.00289248 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189185 | CATCCTCGAGGCTCA[-/G]GCCCACTTTCTGCAG | 996 |
rs775088499 | snp | A/G | 3.30458e-05 | 0.0040647 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151904 | TGTTCCAGTTTGGCC[A/G]ATTCTGGCAACAGAC | 996 |
rs775147698 | snp | A/C | 7.27934e-05 | 0.00603253 | intron-variant | CDC27 | GRCh38.p7 | 17:47144032 | TTACTTGATTTATGA[A/C]CATTAACCATTGTTT | 996 |
rs775216298 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47154089 | GCGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 996 |
rs775229952 | snp | A/C | 1.66935e-05 | 0.00288903 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157082 | AATCTGTATTCAAGG[A/C]GTACTTTGAATTGGA | 996 |
rs775231891 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187042 | GCTTGTTCTTCTCAC[C/T]GTTCCAAATCCATTC | 996 |
rs775268664 | snp | A/G | 0.00163905 | 0.0285804 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137349 | GAAACAGTTCCCTGC[A/G]GCACACCAGGCCTTA | 996 |
rs775286853 | snp | A/G | 0.00176282 | 0.0296362 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142312 | ATGATGGAAGAGTCC[A/G]ATTTTGTAATTTCCA | 996 |
rs775287976 | snp | C/T | 2.20699e-05 | 0.00332182 | intron-variant | CDC27 | GRCh38.p7 | 17:47121032 | ACTTTAAAAATAAAA[C/T]AGAAGTCCACAGTAA | 996 |
rs775321736 | snp | C/T | 4.95503e-05 | 0.00497722 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137288 | GATCAACTTGGATAG[C/T]TCTCTGGAAGAATTT | 996 |
rs775323257 | in-del | -/TAT | 8.38272e-05 | 0.00647353 | intron-variant | CDC27 | GRCh38.p7 | 17:47132232 | GGGAGATTAATAGAG[-/TAT]TAATGTTTAGAAAGC | 996 |
rs775374788 | snp | A/G | 5.01752e-05 | 0.0050085 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132353 | TTTTTCTTGCTTGTA[A/G]TAAATCATTCCTAAA | 996 |
rs775435782 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139083 | TGATGTAACCATATT[C/G]ACAGTCAACCTAGTA | 996 |
rs775457609 | snp | A/C | 0.000487862 | 0.0156107 | intron-variant | CDC27 | GRCh38.p7 | 17:47157137 | TTCCTGAAACAGAAA[A/C]TTTCTACCAAGTCAT | 996 |
rs775461565 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182734 | AAACATATCAAAATC[A/C]AAAATGTATTTTATC | 996 |
rs775477257 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182604 | AATACAATCATATTG[C/T]ATACATTCTGCTACG | 996 |
rs775485017 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177779 | GTTCCATAGGTAGCA[A/C]TTACTTATGAAAAAA | 996 |
rs775547845 | snp | C/T | 1.77442e-05 | 0.00297855 | intron-variant | CDC27 | GRCh38.p7 | 17:47142071 | AAAAACGCAATAAAC[C/T]AGTCTGCTTCTCTAG | 996 |
rs775593240 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167250 | AATGCAACTTTTTTC[A/T]ACAGAGTAATATTTA | 996 |
rs775641781 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120474 | ATTGTTCCATCTGGC[A/C]CTTGCAAACACCATT | 996 |
rs775670987 | snp | A/G | 4.29655e-05 | 0.00463475 | intron-variant | CDC27 | GRCh38.p7 | 17:47156865 | ATATGAGTTATCATA[A/G]GATCATTTGGTATTA | 996 |
rs775710671 | in-del | -/AGGAAGGAAGGA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175052 | GAGAGGAAGGAAGGA[-/AGGAAGGAAGGA]AGGAAGGAAGGAAGG | 996 |
rs775725524 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47163461 | ATCCCAGCACTTTGG[A/G]AGGCTGAGGTGCCAG | 996 |
rs775756315 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186461 | GTGAAGTCTTACCCC[-/T]AGGAATAATTGCTAA | 996 |
rs775782611 | snp | A/G | 0.00214916 | 0.0327103 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138769 | ATCCATGTCTGTTAA[A/G]TCTTTTGACAGAACT | 996 |
rs775794094 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146373 | GTTCTTGTTGGGGAC[A/T]GTGATCTTAACCTGT | 996 |
rs775842128 | snp | A/G | 3.32734e-05 | 0.00407868 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171963 | GGTATTTGCATTGCG[A/G]TGTAGTACAACTGTG | 996 |
rs775887564 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187963 | AAGATATAATCTTAC[A/G]TTTTATTAATTCAAA | 996 |
rs775911189 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172715 | TTACATTAGGAAATG[C/T]CCCCTGCCTTCTTAA | 996 |
rs775964025 | snp | C/T | 1.73459e-05 | 0.00294494 | intron-variant | CDC27 | GRCh38.p7 | 17:47123870 | CACTGTTTGGGACCA[C/T]GACCCCAGTCTTTAC | 996 |
rs775974115 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130705 | CATGATGAAACCCCC[A/G]TCTCTACTAAAAATA | 996 |
rs776017641 | snp | A/G | 1.65176e-05 | 0.00287376 | synonymous-codon, intron-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47122571 | GAAATTCATCAGGGC[A/G]AGGTGCGTTTGACCT | 996 |
rs776067003 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149897 | GAGGTGGAGGTTGCA[A/G]TGAGCCGAGATTGCA | 996 |
rs776106384 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47151078 | TTAGTCTATTTGTTT[A/G]ACTCTAAAGTGAAAT | 996 |
rs776145016 | snp | C/G | 1.65362e-05 | 0.00287538 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137181 | TCTAGGATTGACTCT[C/G]ATAGCATTTCGAAAA | 996 |
rs776164646 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170686 | AGGAACAGAAGATGA[G/T]TACTATACTGGGGGA | 996 |
rs776229474 | in-del | -/G | 1.81177e-05 | 0.00300974 | intron-variant | CDC27 | GRCh38.p7 | 17:47137372 | AGGCCTTAAAAAAAT[-/G]GGAACAAAAACCAAA | 996 |
rs776257806 | in-del | -/AT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125918 | CACAATTCAGAATTG[-/AT]ATGTTTTCTTTCTAT | 996 |
rs776266191 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179585 | AATATTAAATACTTA[A/G]AGTACCTAGTATACA | 996 |
rs776278848 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127763 | GCTGAAGTGCAGTGG[C/T]GCGAAAACAGCTCAC | 996 |
rs776306161 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182473 | CCCCAAAGAGGAAAC[A/C]ACCACACTGAATTTT | 996 |
rs776334668 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118687 | TTGCTTGATCAAAAT[A/G]TGTTCTTCTTCGGGT | 996 |
rs776359371 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140777 | TGGGTTTTGTAGCAA[C/T]GAATAAGACTTTCTG | 996 |
rs776378939 | snp | C/T | 2.72164e-05 | 0.00368883 | intron-variant | CDC27 | GRCh38.p7 | 17:47181675 | ATAAATATACATACA[C/T]ACAGACTTTCAAGGT | 996 |
rs776528390 | snp | A/G | 3.51235e-05 | 0.00419052 | intron-variant | CDC27 | GRCh38.p7 | 17:47142062 | AACAAAGGAAAAAAC[A/G]CAATAAACTAGTCTG | 996 |
rs776570725 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164015 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAATGC | 996 |
rs776638964 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153021 | ATATTTTCATCTAAT[A/G]TACCACCACTTCAAA | 996 |
rs776649517 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181385 | CAATTCTACATAGTT[A/C]TTAAAAGTAGTATGT | 996 |
rs776659941 | in-del | -/A | 1.72169e-05 | 0.00293396 | intron-variant | CDC27 | GRCh38.p7 | 17:47151967 | TATGGGCTGCACTGT[-/A]AATGATAAAAGACAA | 996 |
rs776666660 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137666 | GCAGAGATGACCAGG[A/G]ACAGAAACTCTGTGG | 996 |
rs776668525 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125466 | TGGCCAGCTGGTCTC[A/G]AACTTCTGACCTCAA | 996 |
rs776668817 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118735 | ATGCAAAAAACAAAA[C/T]CAAACAAAAAAAGAA | 996 |
rs776780715 | snp | C/T | 1.67545e-05 | 0.0028943 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141991 | CAAAGCTAAATAACC[C/T]TTCCCCATTTCACGA | 996 |
rs776793547 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120350 | GGGATATTTGATTCC[C/T]ACATACGAGTCCCAA | 996 |
rs776819129 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165246 | TGTTTCCAGTTTTGG[A/G]CTTTTATGAATAAAG | 996 |
rs776848963 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177643 | AAACAGTAGACCTTA[A/C]GCAATTTTGAACTCT | 996 |
rs776930242 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159944 | CCGTGGCCTCGGTCC[C/T]GGCCCCATCCACGGC | 996 |
rs776947462 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149511 | TGAGACTCTGTCTTA[-/A]AAAAAAAAAAAAAAA | 996 |
rs777010411 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146455 | ATAGTGAAGAAACTA[-/C]CCAAAGCTGGGGAAA | 996 |
rs777036449 | snp | A/G | 3.39305e-05 | 0.00411875 | intron-variant | CDC27 | GRCh38.p7 | 17:47129567 | CCTCTTGATATTTAT[A/G]AAGAAAGGTGAGAAC | 996 |
rs777050526 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161027 | AGTTTTATCAAAGTC[C/T]GTATCTAAGATCATT | 996 |
rs777196007 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145431 | TGTTTGAGTGTTATA[C/T]AATAAAGAATTTGTC | 996 |
rs777197917 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161681 | CTTGCATCCTGGAGG[C/T]GGAGGTTACAGTGAG | 996 |
rs777254398 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130168 | AGATCGAGACCATCC[C/T]GGCTAACACGGTGAA | 996 |
rs777434535 | snp | G/T | 3.35227e-05 | 0.00409393 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141894 | AGGCCCTTCCAATTT[G/T]GCACAGTACCCAACC | 996 |
rs777461230 | snp | A/G | 0.000117083 | 0.00765036 | intron-variant | CDC27 | GRCh38.p7 | 17:47129343 | AAAACAAGGGATAAC[A/G]TTGTTTTTAAGCAAT | 996 |
rs777488242 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162523 | GCTTTGCCAGCAGAA[G/T]GTGATATAAAACAGA | 996 |
rs777495484 | snp | C/T | 6.60578e-05 | 0.0057467 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129498 | ATCCAAAGCCTTCTC[C/T]GATTTTTTCAGTGCA | 996 |
rs777521386 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187704 | GGGGCCAGAGAAGGC[-/A]AAAAAAAAAAAATCA | 996 |
rs777533721 | in-del | -/GGTCT | 0.0021605 | 0.032796 | intron-variant | CDC27 | GRCh38.p7 | 17:47157130 | GTTTAATTCCTGAAA[-/GGTCT]CAGAAAATTTCTACC | 996 |
rs777613532 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151869 | TCTCGGCTATTTCCA[C/T]TCTGTGAGAAGACAG | 996 |
rs777628823 | snp | A/T | 0.000380093 | 0.0137805 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157361 | ATGTGAATTTAAATG[A/T]TTGGTCAGGATCTGG | 996 |
rs777664015 | snp | G/T | 8.5242e-05 | 0.00652792 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158284 | AACATTCTGATCCTT[G/T]GGCAAGCCGATCTGT | 996 |
rs777675452 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47139234 | TCAAAAACCTCATTT[A/C]CAAGTTTTAATAATG | 996 |
rs777678685 | snp | A/T | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137260 | AATAGAGTATAGGCA[A/T]AAGCGTAATTTGGAT | 996 |
rs777682376 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155718 | CACTTTGGGAGGCCA[C/T]AGCAGGAGGATCACT | 996 |
rs777694893 | in-del | -/GAG | 1.80338e-05 | 0.00300276 | intron-variant | CDC27 | GRCh38.p7 | 17:47158163 | GCAGGAAAAAAAGAA[-/GAG]GAGATGGGAACCCAC | 996 |
rs777753298 | snp | G/T | 1.70342e-05 | 0.00291836 | intron-variant | CDC27 | GRCh38.p7 | 17:47151956 | GGTTTGTGAATTATG[G/T]GCTGCACTGTAAATG | 996 |
rs777859701 | snp | A/G | 1.69344e-05 | 0.00290979 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189207 | TTTCTGCAGTGCCTC[A/G]GGCCCCCCCTGTAGC | 996 |
rs777874105 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167917 | AATTGGGATTCCCAC[A/C]ATGCTCTATTCAGGT | 996 |
rs777898998 | snp | G/T | 1.70098e-05 | 0.00291627 | intron-variant | CDC27 | GRCh38.p7 | 17:47169897 | ATGCTTTTCTGACAG[G/T]TTGAATCATTCTTAC | 996 |
rs777918542 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47152868 | GCCCTTTATCCTTCT[A/G]CTATTTTTAAATTAG | 996 |
rs777964743 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183732 | ACTCCACAAGGTAGG[A/G]GCTACGTCTGTTTTT | 996 |
rs777995806 | snp | C/T | 1.81734e-05 | 0.00301436 | missense, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120972 | GCATGAAGTTGTGTG[C/T]CATCCGCATCTGTCA | 996 |
rs778094775 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47138638 | AAAAAAGAAATAAGC[A/G]TGGGTGACACTAAAT | 996 |
rs778111166 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47153748 | TTTTAAAAATGGTAT[C/T]TTGGCCTCTATTTCC | 996 |
rs778112946 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137623 | GAGGTTGAATAATGT[A/G]ACTCTACCTTCTTGT | 996 |
rs778139018 | snp | C/T | 0.0123139 | 0.0774941 | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47157126 | AATCTGTTTAATTCC[C/T]GAAACAGAAAATTTC | 996 |
rs778179915 | snp | A/G | 1.66205e-05 | 0.00288271 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157058 | CTGAATCAATATAAG[A/G]CACTGAGGAATCTGT | 996 |
rs778227848 | snp | A/G | 1.69815e-05 | 0.00291384 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154716 | CATCAATTACAGGAG[A/G]TGTATTAGTGTAGTT | 996 |
rs778228926 | snp | C/T | 1.74705e-05 | 0.00295549 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142283 | GTGTGATTGTGGATA[C/T]TTTCCCTTCTGAAAT | 996 |
rs778246684 | in-del | -/TA | 1.67225e-05 | 0.00289154 | intron-variant | CDC27 | GRCh38.p7 | 17:47122431 | ACTCAAAATCATATG[-/TA]TATGATACTTACTGA | 996 |
rs778248009 | snp | A/C | 0.000256922 | 0.0113311 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171934 | GCTGAGATCAACACA[A/C]CATTTTGCAAGCAGG | 996 |
rs778254548 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161147 | TCCTGCCTCAGCCTC[A/C]CAAGTAGCTGGGACT | 996 |
rs778363916 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161569 | CAGCCTGGCCAACAC[A/G]GTGAAAACTCGTCTC | 996 |
rs778379794 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132298 | AACTTTGAGGGTTGA[C/T]ATCAAGCGCTTTTTG | 996 |
rs778379805 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132584 | AAAAAATTTTTTTTT[G/T]AATTAGGGTCTCACT | 996 |
rs778383610 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121180 | ATGCAACTCAAGTTT[C/T]CTAACTTTATAATAG | 996 |
rs778451795 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177478 | GCTACTCAGGAGGCT[A/G]ATGCAGGAGAATTGC | 996 |
rs778508192 | snp | G/T | 3.3865e-05 | 0.00411477 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141858 | CTATACTTACTTGCA[G/T]GTACTCTGAAAGTTC | 996 |
rs778562438 | snp | C/T | 1.66125e-05 | 0.00288201 | intron-variant | CDC27 | GRCh38.p7 | 17:47121066 | TTCTGACAAATATGT[C/T]CTGTTGGTTCATGAA | 996 |
rs778566981 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134873 | CAAGTAATCTTCCAG[C/T]TTCAGCTTCCTAAAG | 996 |
rs778577824 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162324 | CTAATTAATGTCTTG[A/C]CTCTTCATCCCTTCA | 996 |
rs778580407 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119843 | CCCAATTACTCTTAG[G/T]AAATGTTTTGGTGAC | 996 |
rs778622621 | in-del | -/CTT | 1.80406e-05 | 0.00300333 | cds-indel, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181562 | GAATAGATTTCAAAC[-/CTT]CTGCATAAAGGCGTT | 996 |
rs778669819 | snp | C/T | 2.26406e-05 | 0.00336449 | intron-variant | CDC27 | GRCh38.p7 | 17:47154888 | AAGAGAATGGCAAAT[C/T]AGTCTTAGGGACAGT | 996 |
rs778726431 | in-del | AAGCCAAGTATGACTGTGAGTTATTTATCTTTATATTCAAGC/CCAGTGT | | | | | GRCh38.p7 | 17:47168522 | TTTATCTTTATATTC[lengthTooLong]CAAGTGTGTTTAGCT | 996 |
rs778807988 | snp | C/T | 3.49071e-05 | 0.0041776 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143954 | TTGGGGGAGATGTAA[C/T]AGTGGGGCTCAATAC | 996 |
rs778827644 | snp | A/C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185473 | CAGGCGTGAGGCACC[A/C/G]CGCCCGGCCTGTAAT | 996 |
rs778895847 | snp | A/T | 0.000131965 | 0.0081219 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151831 | GACCAGAACTTTGTG[A/T]TTGTGCAAGAATTGG | 996 |
rs778936263 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47171736 | TATTATTTATTACCA[C/T]AACAATGAAATCTCC | 996 |
rs778944605 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47154151 | TAAGTATACTACCAA[A/G]TATTTTTCATTTTCA | 996 |
rs778948685 | in-del | -/AAAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147404 | CTCCGTCTCAAAAAC[-/AAAC]AAACAAACAAACAAA | 996 |
rs778959185 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175659 | CATCTCTACTAAAAA[C/T]ACAAAAATTAATCAG | 996 |
rs778969516 | in-del | -/CTTGAACCTG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130793 | GAGGCAGGAGAATCA[-/CTTGAACCTG]GGAGGTGGAGGTTGT | 996 |
rs779047163 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47166458 | AGGTAGTGATATTCC[C/T]TCTTTCATTCCTGAT | 996 |
rs779125330 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135228 | GTTTGGCTTCCTTGT[C/T]CCCCACTTACTGTTA | 996 |
rs779126240 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144228 | CTTCACCTTGTGATC[A/G]TAAGTCAATAATCCT | 996 |
rs779126942 | snp | C/T | 4.94523e-05 | 0.00497229 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137247 | AAACTCATGCCCTAA[C/T]AGAGTATAGGCATAA | 996 |
rs779135723 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47182266 | CATAGGAATAACTTT[A/T]AATTTTTTGAATATA | 996 |
rs779180628 | in-del | -/TTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179631 | GTGATAGAATTATTG[-/TTA]TTATTACTGAGCCAG | 996 |
rs779213722 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150980 | GAGGTTGTGGTGGGC[C/T]GAGATCACACCACTG | 996 |
rs779230580 | in-del | -/AA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47143985 | CTGAGGTGTTGTACT[-/AA]AAAAAAATTATAAAG | 996 |
rs779271397 | snp | C/G | 1.6674e-05 | 0.00288734 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189167 | GGGTTCCTGCAGCAC[C/G]GTCATCCTCGAGGCT | 996 |
rs779367027 | in-del | -/ACAGG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174969 | AACAGGACTATCGAA[-/ACAGG]ACAGGACAGGACAGG | 996 |
rs779379145 | snp | A/T | 0.000793165 | 0.0198986 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169957 | GAGTAAAGCAAGCTG[A/T]ATCACCAAACTCAGT | 996 |
rs779404886 | snp | A/G | 1.91433e-05 | 0.00309375 | missense, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120939 | ATTTCCAGAAGTTAA[A/G]ATTCATCACTTTCAG | 996 |
rs779409083 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175437 | TAGAGTACTCTGTGG[C/G]TACCCTGTCATGAAC | 996 |
rs779410246 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47129950 | ATATTCACATTTCAT[-/C]AGGTTTATGCGGTCT | 996 |
rs779411674 | in-del | -/TTTAAAG | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190771 | AGTAGCCATTAGCTA[-/TTTAAAG]TTTAAGTTAAAATGA | 996 |
rs779413620 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133362 | AGGCTGGTCTTGAAC[C/T]CCTGACCTCAGGTGA | 996 |
rs779424403 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185834 | TCTAGGATACTGATT[C/T]AGTTTAGATGCACGT | 996 |
rs779438688 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137501 | CTCAATTCTAATTAT[A/T]CACAGATTCCATATT | 996 |
rs779450686 | snp | C/T | 1.67013e-05 | 0.0028897 | intron-variant | CDC27 | GRCh38.p7 | 17:47129538 | TGTAAGAAATAAAGA[C/T]CATGTTAATACTCCC | 996 |
rs779462443 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131612 | GAAGCTAATAAATGC[A/G]ATTTTAAAAAGCAAA | 996 |
rs779488332 | snp | A/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190850 | GGATTCAGTAGCCCT[A/G]TATGTGGCTAGTGAC | 996 |
rs779492361 | snp | C/G | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47132289 | GTAAAACTGAACTTT[C/G]AGGGTTGATATCAAG | 996 |
rs779501896 | snp | A/G | 8.56597e-05 | 0.00654389 | intron-variant | CDC27 | GRCh38.p7 | 17:47142032 | TCAAACCTTCTAGGA[A/G]AAAACAACATAGTAA | 996 |
rs779583236 | snp | C/T | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47191284 | TTTGGAAACAATCTA[C/T]CACGCTAGATATGAG | 996 |
rs779593188 | snp | C/T | 1.74854e-05 | 0.00295676 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157117 | TCTAAATTCAATCTG[C/T]TTAATTCCTGAAACA | 996 |
rs779631769 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159666 | TAACACCCAGACCGA[C/T]GTGGCCATTGTAGTC | 996 |
rs779651751 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134863 | CTCCTGGTCTCAAGT[A/G]ATCTTCCAGCTTCAG | 996 |
rs779700421 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117833 | CTCTAGTTTTTTGTG[A/C]AACATAAAACTGTAT | 996 |
rs779780545 | in-del | -/AT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177880 | CACACACACACACAC[-/AT]ATCTCCAAAGAGCTA | 996 |
rs779792842 | snp | G/T | 1.9618e-05 | 0.00313187 | intron-variant | CDC27 | GRCh38.p7 | 17:47171897 | AAAACAAAATAGCTA[G/T]AAAATATTTTAAAAC | 996 |
rs779810194 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145685 | AGGCAGGCGGATCAC[A/G]AGGTCAAGAGATCGA | 996 |
rs779830267 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160813 | GAACTATGAAGAAGG[C/T]ACCCTTGGGGAACCA | 996 |
rs779895176 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128272 | CTGACCTCAAGTGAT[C/T]TGCCCACCTTGGCCT | 996 |
rs779896547 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119498 | TAAGTTTGTCCTCCA[C/T]CAAATAATCCAGAAT | 996 |
rs779903185 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144646 | CCTGAGATATGAGAA[C/T]TTCAATCTTAGCAAG | 996 |
rs779927178 | snp | C/T | 1.66582e-05 | 0.00288597 | intron-variant | CDC27 | GRCh38.p7 | 17:47138713 | AAAAAGGTAACTATA[C/T]AAGCAAAGTATTTTG | 996 |
rs779983433 | in-del | -/TTTGTG | 3.30082e-05 | 0.00406239 | cds-indel, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151825 | TTTGTGGACCAGAAC[-/TTTGTG]TTTGTGCAAGAATTG | 996 |
rs780048570 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173396 | AAAAAAGAATGGGGC[A/G]CTCACTGCAGTAGGA | 996 |
rs780059853 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119592 | ATAAAATGTTAACAA[-/C]TAAAATTTCTCTAAA | 996 |
rs780082827 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185114 | TATTCTTAAATATAA[A/T]ATATTATTTAAAATA | 996 |
rs780105633 | snp | A/C | 1.74805e-05 | 0.00295634 | intron-variant | CDC27 | GRCh38.p7 | 17:47122624 | AAACAGCAGCACTAC[A/C]TTTTTCATTAAGTTG | 996 |
rs780117027 | snp | A/G/T | 3.6649e-05 | 0.00428058 | intron-variant | CDC27 | GRCh38.p7 | 17:47137149 | TACTTCATTACCACT[A/G/T]ACCATGCATTATAAT | 996 |
rs780120871 | snp | C/T | 0.000125982 | 0.00793569 | intron-variant | CDC27 | GRCh38.p7 | 17:47143833 | AATGAACAGAAATGT[C/T]AGCAGGCGAAGCATT | 996 |
rs780144743 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47142760 | CTCACCGCAACCCAA[-/C]CTCTGCCTCCCGGGT | 996 |
rs780158747 | snp | A/G | 0.00018377 | 0.0095839 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138816 | TTTGAAGATGCCAAA[A/G]TGTTGTAGAGTAGAT | 996 |
rs780160708 | snp | C/T | 1.66062e-05 | 0.00288146 | splice-donor-variant | CDC27 | GRCh38.p7 | 17:47122443 | TATGTATGATACTTA[C/T]TGATCTGTTCTTCTT | 996 |
rs780161838 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140458 | TAAAAGACCTACCAG[A/C]CAAATATAGGTAGGT | 996 |
rs780175089 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184012 | AAATTACTCCTTTAT[A/G]AAATCTGGGATTTCC | 996 |
rs780193340 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180559 | TACTAAACCCATACT[A/G]TTTGACTTGTAAATT | 996 |
rs780247819 | in-del | -/AGTTGCTAAAGTTCTGTAAAGATGTGAATTTAAA | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157325 | AAGAGTTGGGCAGAC[lengthTooLong]TGTTTGGTCAGGATC | 996 |
rs780282676 | snp | C/T | 1.69732e-05 | 0.00291313 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143938 | CTTCGAGGCAGTGCG[C/T]TTGGGGGAGATGTAA | 996 |
rs780300060 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125071 | TACAGGGGCTTACCT[G/T]TAATGCCTAATTTTG | 996 |
rs780320642 | in-del | -/TATA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127365 | AATTACTAGATAAAT[-/TATA]TATATATTTAATCCC | 996 |
rs780351105 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47164803 | GCCTGAGCGACAGAG[C/T]GCAAGATTCCATTTC | 996 |
rs780408665 | snp | A/G | 4.99438e-05 | 0.00499694 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157035 | GACAGTATCAGGTGA[A/G]ATTACAGCTGAATCA | 996 |
rs780523901 | snp | A/G | 3.31538e-05 | 0.00407134 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141937 | GTGAGAAGGTAGATG[A/G]CTCAAAATATTTATA | 996 |
rs780531497 | snp | A/T | 0.000247633 | 0.0111245 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137218 | AATGCTTTGTCCAAT[A/T]CTTCAGTTAAGACAA | 996 |
rs780547917 | snp | A/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189683 | TGAAGCAAAGGGTGA[A/G]ACAGCAGAGTTTGGG | 996 |
rs780559817 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156207 | GCAGTGACACCATCT[C/G]GGCTCACTGCAACCT | 996 |
rs780612060 | snp | G/T | 1.70409e-05 | 0.00291893 | missense, splice-acceptor-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142024 | AAGGCTCATCAAACC[G/T]TCTAGGAGAAAACAA | 996 |
rs780613746 | snp | C/T | 1.67189e-05 | 0.00289122 | intron-variant | CDC27 | GRCh38.p7 | 17:47129349 | AGGGATAACGTTGTT[C/T]TTAAGCAATACAACA | 996 |
rs780654188 | snp | C/T | 0.00491628 | 0.0493353 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156943 | CTAAGAGCTGCTGGT[C/T]CTCCTAATAAACTTC | 996 |
rs780661483 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179357 | AACTGTTGCCAAGAA[A/T]TCTGAGGTTGGTTCA | 996 |
rs780673219 | in-del | -/C/CA/CACCC | 5.13822e-05 | 0.00506838 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189209 | CTGCAGTGCCTCAGG[-/C/CA/CACCC]CCCCCCCTGTAGCGG | 996 |
rs780748522 | in-del | -/AAA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178554 | ATAAATAAAAATAAG[-/AAA]AAAAAAAAAAAACCC | 996 |
rs780769166 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174055 | GCCGAGATCGTGCCA[C/T]CGCATTCCAGCCTGG | 996 |
rs780799591 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159137 | GACCAGGTTTTTATT[G/T]GTTGTTGTTTTTTTT | 996 |
rs780825192 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47159525 | AGTGGCCTGTCACCT[C/T]GCAAGGGACGGCGTA | 996 |
rs780834894 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150596 | TTGATTTTGGACTTA[C/T]GGCTTTACAACTGTA | 996 |
rs780844929 | snp | A/C | 1.65916e-05 | 0.00288019 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129519 | TTTCAGTGCATGTTG[A/C]ACCTGTAAGAAATAA | 996 |
rs780851392 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47149018 | CGGGAAGCAGAGGTT[G/T]CAGGGAGCCAAGATT | 996 |
rs780857057 | snp | A/G | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189340 | GGAATACCCGAAGTG[A/G]AGAAAGCCGAGCGGG | 996 |
rs780947905 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144388 | CTCTGGATCGACAAA[A/T]GATAAGCACATCTAT | 996 |
rs780992405 | snp | A/G | 0.00296878 | 0.0384137 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169943 | TCCCAACAATGAAAG[A/G]GTAAAGCAAGCTGAA | 996 |
rs781023793 | snp | A/C/T | 5.04226e-05 | 0.00502087 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137343 | CAGACTGAAACAGTT[A/C/T]CCTGCAGCACACCAG | 996 |
rs781059013 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117715 | CCATTGTTTTTGTCA[C/T]AGTATTTATTTTGAT | 996 |
rs781080212 | snp | A/G | 3.46129e-05 | 0.00415996 | intron-variant | CDC27 | GRCh38.p7 | 17:47151971 | GGCTGCACTGTAAAT[A/G]ATAAAAGACAACACA | 996 |
rs781103968 | snp | G/T | 0.000251894 | 0.0112198 | intron-variant | CDC27 | GRCh38.p7 | 17:47158168 | AAAAAAAGAAGAGGA[G/T]ATGGGAACCCACCCA | 996 |
rs781165749 | snp | A/G | 1.66749e-05 | 0.00288741 | intron-variant | CDC27 | GRCh38.p7 | 17:47138703 | GAGGGTGATCAAAAA[A/G]GTAACTATATAAGCA | 996 |
rs781168964 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144461 | AGAGAAAAAAGAAAA[A/G]ACAGTTGGGCAAAGA | 996 |
rs781175251 | in-del | -/CG/CGTAAGAAAGGTCTCAGGCTGTCTG | 0.00540408 | 0.0517524 | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47157125 | AATCTGTTTAATTCC[-/CG/CGTAAGAAAGGTCTCAGGCTGTCTG]TGAAACAGAAAATTT | 996 |
rs781230658 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155276 | TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCCAGG | 996 |
rs781241917 | in-del | -/AG/T | 1.72895e-05 | 0.00294015 | intron-variant | CDC27 | GRCh38.p7 | 17:47157407 | ACAAAAAAAAAAAAA[-/AG/T]GTTTGTCTCTGAGGA | 996 |
rs781261216 | snp | C/T | 1.72856e-05 | 0.00293982 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142411 | ATTTTAGGTGGAAAC[C/T]TCATTTTTAATTTTT | 996 |
rs781287699 | snp | A/T | 0.0106847 | 0.0723064 | intron-variant | CDC27 | GRCh38.p7 | 17:47157128 | TCTGTTTAATTCCTG[A/T]AACAGAAAATTTCTA | 996 |
rs781312678 | snp | A/G | 1.70761e-05 | 0.00292194 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157236 | GACACTTACAATTGT[A/G]TCCTGGGGTGTTTCC | 996 |
rs781346820 | snp | C/T | 0.000164916 | 0.00907914 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129441 | TCTGTGAAATTTGCA[C/T]AGAGGGTTCTTGGGA | 996 |
rs781398649 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144611 | AGGAGCCTCTGTACA[-/T]TTTTACTTTAAAGGC | 996 |
rs781420819 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124705 | ACAGCTAGATTCTCA[C/T]ATCTATCTGCTTCTC | 996 |
rs781470262 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179006 | GGGGTTTCTCCATGT[C/T]GGTCAGGCTGGTCTC | 996 |
rs781516523 | snp | G/T | 3.93809e-05 | 0.00443722 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142306 | TCTGAAATGATGGAA[G/T]AGTCCAATTTTGTAA | 996 |
rs781529171 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123234 | TTTACAGTGATTTTA[A/T]ATTGAGTTATATCAA | 996 |
rs781547364 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121497 | GGCTGGAGTGCAGTG[A/G]CACAATCATAGCTCA | 996 |
rs781548146 | snp | C/G | 3.5664e-05 | 0.00422264 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181567 | GATTTCAAACCTTCT[C/G]CATAAAGGCGTTCTG | 996 |
rs781549305 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140262 | GGACCACAGGTGAGT[G/T]CCACCACACCCAGCT | 996 |
rs781555306 | snp | C/T | 5.0872e-05 | 0.00504316 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143936 | TTCTTCGAGGCAGTG[C/T]GTTTGGGGGAGATGT | 996 |
rs781592140 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180279 | TTTCTAAGCCTTCCA[C/T]TCCTTCTCACCTTTC | 996 |
rs781611418 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47184845 | AAATCAGCACCTCTG[A/C]CCAACTGATGGTGTG | 996 |
rs781635053 | snp | A/G | 4.07208e-05 | 0.00451206 | intron-variant | CDC27 | GRCh38.p7 | 17:47137113 | GTAAGTACCAGCACC[A/G]TCAATACGACTTTGT | 996 |
rs781648392 | in-del | -/TTT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123403 | TACTTTTTTTTCTAC[-/TTT]TTTTTTTTTTTTTTT | 996 |
rs781660548 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181035 | GGCAGGTGGATCACC[-/T]AAGCTCAGGAATTTG | 996 |
rs781663205 | snp | C/T | 0.000369344 | 0.0135844 | intron-variant | CDC27 | GRCh38.p7 | 17:47154910 | AGGGACAGTGAGGAT[C/T]TGAGGGGCAGATTAA | 996 |
rs781728880 | in-del | -/ATATACAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133025 | TATATATATATATAT[-/ATATACAC]ACACACACACACACA | 996 |
rs781748297 | snp | G/T | 4.4239e-05 | 0.00470293 | intron-variant | CDC27 | GRCh38.p7 | 17:47172096 | TTTAAAAAGGCTATT[G/T]TTCAGTATATTGAAT | 996 |
rs781770570 | snp | C/G/T | 5.60746e-05 | 0.00529478 | intron-variant | CDC27 | GRCh38.p7 | 17:47137145 | TTTGTACTTCATTAC[C/G/T]ACTTACCATGCATTA | 996 |
rs796076888 | multinucleotide-polymorphism | CA/TT | | | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157354 | GTAAAGATGTGAATT[CA/TT]AATGTTTGGTCAGGA | 996 |
rs796080710 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133752 | CCTGGCCTACATATA[-/T]TTTTTTTCTTTTTTG | 996 |
rs796119332 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136685 | TAAATAAAAGGGTAC[A/G]CTAAGTTCTTAATAG | 996 |
rs796126227 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141946 | TAGATGGCTCAAAAT[A/G]TTTATAGCTTCTTTG | 996 |
rs796146622 | in-del | -/AC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147427 | CAAACAAACAAACAA[-/AC]AAAAAAAAAAACACT | 996 |
rs796155589 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189265 | TTTAAACTCACCAGC[C/G]ACCGTTACCGGGGGA | 996 |
rs796168524 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136707 | TCTTAATAGTAACTC[A/C]ATAAACCAGAACACT | 996 |
rs796188286 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135859 | TTAAGAACTGAGTTC[C/T]TGGCCGGGTATGGTG | 996 |
rs796204387 | multinucleotide-polymorphism | AAGTA/TTTTC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137050 | CCATCCCTAAGTATA[AAGTA/TTTTC]CCAAATTCATGATAA | 996 |
rs796210783 | multinucleotide-polymorphism | CTTG/TTCA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136816 | TTTCCCAAGCACTTT[CTTG/TTCA]CCCAATCACCATTTC | 996 |
rs796222654 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137250 | CTCATGCCCTAATAG[A/G]GTATAGGCATAAGCG | 996 |
rs796265930 | snp | G/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137285 | TTGGATCAACTTGGA[G/T]AGCTCTCTGGAAGAA | 996 |
rs796299629 | multinucleotide-polymorphism | GC/TG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131876 | GGTCTCGCTATGTTG[GC/TG]CAGGCTGGTCTCCAA | 996 |
rs796299832 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137135 | CGACTTTGTCTTTGT[A/G]CTTCATTACCACTTA | 996 |
rs796302661 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154721 | ATTACAGGAGGTGTA[C/T]TAGTGTAGTTTTGTA | 996 |
rs796316978 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154722 | TTACAGGAGGTGTAT[C/T]AGTGTAGTTTTGTAA | 996 |
rs796321722 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136129 | CCTGGGTGACAGAGC[A/G]AGACTCTGCCTCAAA | 996 |
rs796357779 | multinucleotide-polymorphism | CAG/GAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137024 | AGTTAGAAGTTATTG[CAG/GAC]AGTATGTACCATCCC | 996 |
rs796359371 | snp | C/G | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137251 | TCATGCCCTAATAGA[C/G]TATAGGCATAAGCGT | 996 |
rs796368888 | in-del | -/AA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157395 | TTCACCTGTGAAGAC[-/AA]AAAAAAAAAAAGTTT | 996 |
rs796393121 | multinucleotide-polymorphism | CC/TG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131890 | GCCCAGGCTGGTCTC[CC/TG]ACTCCTGACCTTAAG | 996 |
rs796406016 | in-del | -/AC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123401 | TCTACTTTTTTTTCT[-/AC]TTTTTTTTTTTTTTT | 996 |
rs796409283 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189266 | TTAAACTCACCAGCG[A/G]CCGTTACCGGGGGAT | 996 |
rs796427812 | snp | A/G | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137248 | AACTCATGCCCTAAT[A/G]GAGTATAGGCATAAG | 996 |
rs796455486 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47161491 | CACGGTGGCTCATGC[C/T]TGTAATCTCAGCACT | 996 |
rs796456660 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136478 | GCTTCAGAATTATAC[C/T]TTATCTTGATATTTA | 996 |
rs796457670 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151855 | GAATTGGAGTTACCT[C/T]TCGGCTATTTCCACT | 996 |
rs796494256 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131098 | AAAGCTTACTCTCTT[-/A]ACCTGACAATTTCTT | 996 |
rs796503929 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137054 | TCCCTAAGTATAAGT[A/C]ACCAAATTCATGATA | 996 |
rs796505579 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151874 | GCTATTTCCACTCTG[C/T]GAGAAGACAGACTTT | 996 |
rs796538886 | snp | A/C | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141963 | TTATAGCTTCTTTGC[A/C]GTTGTATGAACACAA | 996 |
rs796555096 | multinucleotide-polymorphism | ACC/GCT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131868 | AGAGATGGGGTCTCG[ACC/GCT]TGTTGCCCAGGCTGG | 996 |
rs796561781 | snp | C/G | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137249 | ACTCATGCCCTAATA[C/G]AGTATAGGCATAAGC | 996 |
rs796562366 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136610 | ACAATATGACCTAGG[G/T]AGTAATTTCCTATGT | 996 |
rs796572277 | snp | A/C | | | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154736 | TTAGTGTAGTTTTGT[A/C]AATAGGATCCATCTC | 996 |
rs796587485 | multinucleotide-polymorphism | ATT/GTC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136801 | GCTATTCCTTTCCAA[ATT/GTC]CCCAAGCACTTTTCA | 996 |
rs796595444 | multinucleotide-polymorphism | AAA/GAG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131855 | AAATTTTTTTTGTAG[AAA/GAG]TGGGGTCTCGCTATG | 996 |
rs796595683 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151862 | AGTTACCTCTCGGCT[A/C]TTTCCACTCTGTGAG | 996 |
rs796641903 | snp | A/C | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154714 | CACATCAATTACAGG[A/C]GGTGTATTAGTGTAG | 996 |
rs796641972 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137062 | TATAAGTAACCAAAT[C/T]CATGATAATAAAGAG | 996 |
rs796673584 | snp | A/T | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141970 | TTCTTTGCAGTTGTA[A/T]GAACACAAAGCTAAA | 996 |
rs796677508 | snp | A/G | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137185 | GGATTGACTCTGATA[A/G]CATTTCGAAAACAAG | 996 |
rs796685691 | snp | A/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141890 | AAATAGGCCCTTCCA[A/T]TTTGGCACAGTACCC | 996 |
rs796699827 | multinucleotide-polymorphism | CGA/GGG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137120 | CAGCACCATCAATAC[CGA/GGG]TTTGTCTTTGTACTT | 996 |
rs796708696 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137051 | CCATCCCTAAGTATA[A/T]GTAACCAAATTCATG | 996 |
rs796731878 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136686 | AAATAAAAGGGTACA[C/T]TAAGTTCTTAATAGT | 996 |
rs796737563 | snp | C/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141947 | AGATGGCTCAAAATA[C/T]TTATAGCTTCTTTGC | 996 |
rs796737598 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186635 | AAATTCTGCCTCATA[G/T]GTGAGACTTTTGTAA | 996 |
rs796739143 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47125521 | AAAGTGCTGGGATTA[A/C]AGGCGTGAGCCATCA | 996 |
rs796742746 | multinucleotide-polymorphism | CG/TA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137099 | ACAAGAAAAATTAGT[CG/TA]GTACCAGCACCATCA | 996 |
rs796753138 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135519 | AGTGGCTTTATATAT[C/G]ATTATACTTGTGTTA | 996 |
rs796762139 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173332 | GAAATTTTGGCAGAT[A/G]TGTTTTAATGAGATG | 996 |
rs796792257 | multinucleotide-polymorphism | ACG/GTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137133 | ACGACTTTGTCTTTG[ACG/GTA]TTCATTACCACTTAC | 996 |
rs796807395 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143981 | ATACCTGAGGTGTTG[C/T]ACTAAAAAAAAATTA | 996 |
rs796836810 | multinucleotide-polymorphism | CG/TA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136518 | TCAGTCCAGAAAAAT[CG/TA]AATAAATGTCAACAG | 996 |
rs796848625 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137052 | CATCCCTAAGTATAA[G/T]TAACCAAATTCATGA | 996 |
rs796852854 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151868 | CTCTCGGCTATTTCC[A/C]CTCTGTGAGAAGACA | 996 |
rs796871080 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47173667 | CTAATAAAGACACCA[A/T]CTATTCTTTTTGTGT | 996 |
rs796876980 | snp | G/T | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141949 | ATGGCTCAAAATATT[G/T]ATAGCTTCTTTGCAG | 996 |
rs796913486 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189295 | ATGGGGGAGGCCGAG[A/C]GATTGCCGAGTGCTT | 996 |
rs796941774 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136865 | AAGCAACAAAGTAAC[A/T]AAACTAAACAAACAA | 996 |
rs796942384 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136675 | GAGATACTGCTAAAT[A/T]AAAGGGTACACTAAG | 996 |
rs796948875 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141943 | AGGTAGATGGCTCAA[A/G]ATATTTATAGCTTCT | 996 |
rs796957545 | in-del | -/TCTCA | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154718 | CAATTACAGGAGGTG[-/TCTCA]TATTAGTGTAGTTTT | 996 |
rs796960319 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181210 | CAGTGAGCTGAGATG[C/G]TCCCACTGTACTCCA | 996 |
rs796969472 | snp | C/G | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137282 | AATTTGGATCAACTT[C/G]GATAGCTCTCTGGAA | 996 |
rs796970029 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168998 | TTTTTTTTTTTCTTT[-/C]TTTTTTTTTTGGAAA | 996 |
rs796971961 | in-del | GTAACAAAACTAA/TCAAGGAACACAACTAAAGAAACACACAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136860 | GAAAAAGCAACAAAG[lengthTooLong]CAAACAAAAAACAAC | 996 |
rs796984536 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136687 | AATAAAAGGGTACAC[G/T]AAGTTCTTAATAGTA | 996 |
rs797013747 | in-del | -/AG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157407 | GACAAAAAAAAAAAA[-/AG]TTTGTCTCTGAGGAA | 996 |