SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1378 | snp | A/G | 0.182825 | 0.240806 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107506 | CATTCTGAAAGACCG[A/G]GAGCCTGGAGGTGTG | 25853 |
rs1052656 | snp | A/G | 0.48978 | 0.0707512 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087362 | ACATCCATAGCCCCC[A/G]TGGCTTTGAGGAGAA | 25853 |
rs1052694 | snp | C/T | 0 | 0 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086582 | ACAGGCTGTAGATTT[C/T]TTAGTTCTCACAGAA | 25853 |
rs1980886 | snp | C/T | 0.172351 | 0.237636 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101103 | GCTTGGGTGACAGAG[C/T]CAGAACCTGTCTCAT | 25853 |
rs1980887 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100919 | GGGTATGGTGGCTCA[C/T]GCCTTTAATCCTAGC | 25853 |
rs2275003 | snp | C/T | 0.493107 | 0.0583 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124862 | CTTCCTCTTTTCGTG[C/T]TCCTTTTTTCACTCA | 25853 |
rs2296897 | snp | C/T | 0.44486 | 0.156619 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089397 | AGCAGTCATCTCAGG[C/T]AGGGGCTTACGCACC | 25853 |
rs2297609 | snp | A/C | 0.097727 | 0.198275 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126790 | CCCTAGATCCCGCCC[A/C]TCTCGTTCCGGCGGT | 25853 |
rs2769704 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097487 | aggcagatcacaagg[C/T]caggagtttgagact | 25853 |
rs2890539 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099360 | cctgtagtcccagct[A/G]caggctggggcagga | 25853 |
rs3061496 | in-del | -/A/AA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101064 | aaaaaaaaaaaaaaa[-/A/AA]GTTGGGGAGGGTTTG | 25853 |
rs3814509 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125495 | TTGACTTTCAGCCCT[C/T]GTAATTCACATTGGT | 25853 |
rs4878553 | snp | G/T | 0.326506 | 0.238006 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108310 | CTGTTCTAAGTGTTA[G/T]GAACACAGCTATGAA | 25853 |
rs4879741 | snp | C/T | 0.333952 | 0.235483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104445 | AGTTGGAAAGATAGG[C/T]GTGGGCCTTGTATGC | 25853 |
rs4879742 | snp | C/T | 0.334182 | 0.235401 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104990 | TCTCATATTAACCAA[C/T]TAAAAAATATGGGCC | 25853 |
rs4879743 | snp | C/T | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108326 | GAACACAGCTATGAA[C/T]GAGAGAAATAATATC | 25853 |
rs4879744 | snp | C/T | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108623 | atggtgaaaacccta[C/T]taaacttacaaaatt | 25853 |
rs4879745 | snp | C/T | 0.391583 | 0.206044 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111724 | AGTCCAAAGGCTAGA[C/T]TGGACTAGGCCATTC | 25853 |
rs4879747 | snp | A/G | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118901 | ACCTGGGAGGCGGAG[A/G]TTGCAGTGAGCCAAG | 25853 |
rs4879748 | snp | C/T | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121848 | CTCAGGAGGCTGAGG[C/T]GGGAGAATCGATTGA | 25853 |
rs4879749 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122569 | acaacctccgcctcc[C/T]gggttcaagcaattc | 25853 |
rs5897559 | in-del | -/T/TT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101085 | TTTTTTTTTTTTTTT[-/T/TT]AAATGAGACAGGTTC | 25853 |
rs7022361 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103490 | TACCCATACACAAAG[A/T]TGTTTATTCGGAACA | 25853 |
rs7030120 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115433 | cgtctctactaaaaa[A/T]acaaaaaattagccg | 25853 |
rs7032075 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112674 | gaggccgaggagggc[A/G]gatcatctgaggttg | 25853 |
rs7044522 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115435 | tctctactaaaaata[A/C]aaaaaattagccggg | 25853 |
rs7047316 | snp | A/G | 0.0551013 | 0.156571 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128302 | gtagcctaggctgga[A/G]tgcagtggcacgatc | 25853 |
rs7470431 | snp | C/T | 0.331642 | 0.236293 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124376 | TGACTTATTTTATCC[C/T]GGCCTATAATTGGGT | 25853 |
rs7846909 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116862 | gacgggtgtgtaatc[C/T]cagctactcgggagg | 25853 |
rs7853415 | snp | C/T | 0.185155 | 0.241444 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095719 | ctggattagggatga[C/T]caatttgTATTGTAA | 25853 |
rs7857551 | snp | A/G | 0.480618 | 0.0965156 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096599 | TCAGAGCGAGACTCT[A/G]CCTCAAAAATAAATG | 25853 |
rs7862025 | snp | C/G | 0.391954 | 0.205789 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090649 | TTGCATACATTATTA[C/G]AGCCAAACCTATTTA | 25853 |
rs7862209 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090940 | tgggattacaggcat[C/G]agccaccgtgcccgg | 25853 |
rs7865341 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091220 | tagtcccagctactc[A/G]ggaggctaaggcagg | 25853 |
rs7871667 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115354 | cccagcactttggga[A/G]gccgaggcgggcgga | 25853 |
rs7875653 | snp | C/T | 0.267908 | 0.249358 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116306 | aggctgcagagatcg[C/T]gccactgaactccag | 25853 |
rs7875661 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109667 | GCTGGTTGTCCTGTA[C/T]GGTCTGGATGAGTCC | 25853 |
rs7875858 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088998 | cctgtggtcccagct[A/T]cttgggaggctgagg | 25853 |
rs10122086 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093129 | gctgggattacaggc[A/G/T]taagccaccacgcct | 25853 |
rs10123087 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094724 | tttagtagagacggg[G/T]tttcaccatgttagc | 25853 |
rs10511914 | snp | C/T | 0.480697 | 0.0963277 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107234 | TGCCCCTTTATCAAA[C/T]ATACACTGTGCCCTA | 25853 |
rs10511915 | snp | A/G | 0.266754 | 0.249438 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107312 | TAATCACTGAGACCC[A/G]TTTAAAAACAAGGCT | 25853 |
rs10511916 | snp | C/G | 0.39709 | 0.20215 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124314 | TCATTTGCCAGTCTT[C/G]TGACATCATGCTATT | 25853 |
rs10624115 | in-del | -/CAACAA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102677 | AACAAACAACAACAA[-/CAACAA]AAAACAAGAACACTT | 25853 |
rs10738923 | snp | A/T | 0.492137 | 0.0622048 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108802 | TGGTCTCAAAAAAAA[A/T]AAATAAATAAATATA | 25853 |
rs10738924 | snp | A/T | 0.498652 | 0.0259235 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108806 | CTCAAAAAAAATAAA[A/T]AAATAAATATATATA | 25853 |
rs10758240 | snp | C/T | 0.469839 | 0.119042 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098112 | CCCACAAATATAGAC[C/T]ACTCAGAGAAATACT | 25853 |
rs10758241 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108812 | AAAAATAAATAAATA[A/T]ATATATATATATATA | 25853 |
rs10814069 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101262 | TTTCATTTTTTTGTA[A/G]AAATGGGGTCTCACT | 25853 |
rs10971903 | snp | C/T | 0.240765 | 0.249829 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087248 | AGCACTCACTACACA[C/T]AGATAAACCCCCTGC | 25853 |
rs10971904 | snp | C/G | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089945 | TAACTCTAAGCTTTT[C/G]TCCATCATATGTTTC | 25853 |
rs10971905 | snp | G/T | 0.392511 | 0.205404 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091423 | AGGCTGAGGTGGGTG[G/T]CCCAAGAGTTTGAGA | 25853 |
rs10971906 | snp | A/T | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092779 | GGTGGCTCCCAACAA[A/T]GGCTTCTGTGGCCAC | 25853 |
rs10971907 | snp | C/T | 0.391583 | 0.206044 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092970 | cctgcctcagcctcc[C/T]gagcagctgggatta | 25853 |
rs10971908 | snp | C/T | 0.480775 | 0.0961398 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092974 | CCTCAGCCTCCTGAG[C/T]AGCTGGGATTACAGG | 25853 |
rs10971909 | snp | A/G | 0.481573 | 0.0972063 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093092 | GACCTCAGGTGATCC[A/G]CCCGCCTCGGCCTCC | 25853 |
rs10971910 | snp | C/T | 0.392511 | 0.205404 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096875 | GGTCAGGGTCCTTTA[C/T]TCCTGTCTCGTGATG | 25853 |
rs10971911 | snp | C/T | 0.393065 | 0.205018 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097063 | TTAAAGCAGGGCACA[C/T]ATGTGAAGGACAGTT | 25853 |
rs10971912 | snp | A/G | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100238 | gagtctcacactgtc[A/G]cccaggctggagtgc | 25853 |
rs10971913 | snp | C/G | 0.333952 | 0.235483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100868 | AGTCTTGAACCCCTG[C/G]CCTCAAGTGATCCTC | 25853 |
rs10971914 | snp | A/G | 0.408871 | 0.193029 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101592 | AGACGGGGTTTCTCT[A/G]TGTTGTTCAGGCTGG | 25853 |
rs10971915 | snp | C/G | 0.39214 | 0.205661 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103620 | gcacttcgagaggct[C/G]aagtgggaggatcgc | 25853 |
rs10971916 | snp | A/C | 0.408359 | 0.193449 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105822 | ggcgcgatctcagct[A/C]actgcaacctctgcc | 25853 |
rs10971917 | snp | C/T | 0.397183 | 0.202082 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106412 | GCCACATCAAAAGCT[C/T]CCTATAAAAGGGCAA | 25853 |
rs10971918 | snp | A/G | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108831 | tatatatatatatat[A/G]aatgaggtggacaag | 25853 |
rs10971919 | snp | A/G | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109326 | GAAGGCTTTGTGCCA[A/G]AAAATGGCTGTGAAC | 25853 |
rs10971920 | snp | C/G | 0.480697 | 0.0963277 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110848 | CTCTACTATCATCAC[C/G]TCTTGCCATGGACTT | 25853 |
rs10971921 | snp | A/G | 0.381891 | 0.212379 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111004 | TTTTTTTTTTTTTTT[A/G]AGACCAAGTCTTGCT | 25853 |
rs10971922 | snp | A/G | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112334 | agcgtggtggttcac[A/G]cctgtaatcccagta | 25853 |
rs10971923 | snp | C/T | 0.391583 | 0.206044 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113541 | GACAGGGTTTCACCA[C/T]ATTAGCCAGACTGGT | 25853 |
rs10971924 | snp | A/G | 0.47726 | 0.104176 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113796 | CCGAAGTGTGCATCA[A/G]TGAATAAATGCATAA | 25853 |
rs10971925 | snp | A/G | 0.144632 | 0.226711 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113969 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGTACCT | 25853 |
rs10971926 | snp | A/T | 0.230603 | 0.249246 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114115 | CTCCGTCTCAAAAAA[A/T]AAAATGTGGCACAGA | 25853 |
rs10971927 | snp | C/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115402 | cgagaccatcctggc[C/T]aacatggtgaaaccc | 25853 |
rs10971928 | snp | C/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115418 | aacatggtgaaaccc[C/T]gtctctactaaaaat | 25853 |
rs10971929 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115437 | tctactaaaaataca[A/G]aaaattagccgggcg | 25853 |
rs10971930 | snp | C/T | 0.350982 | 0.228698 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116085 | AAATAAATCCAGGGC[C/T]GGGTGCGGTGGCTCA | 25853 |
rs10971931 | snp | G/T | 0.333952 | 0.235483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116228 | CGGGCATGGTGGCAG[G/T]CGCCTTTAATCCCAG | 25853 |
rs10971932 | snp | C/G | 0.333952 | 0.235483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116837 | AATACATAAATTAGC[C/G]GGGCACAGTGACGGG | 25853 |
rs10971933 | snp | C/T | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117073 | CCTACACAAGATGGA[C/T]TACACTACTAGCTAG | 25853 |
rs10971934 | snp | C/T | 0.258565 | 0.249853 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117712 | CTGAGGTTGGGATTT[C/T]GAGACCAGCCTCACC | 25853 |
rs10971935 | snp | A/G | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118147 | TTTTTTTTCCAAGAT[A/G]GAAAAAAAGACAGAC | 25853 |
rs10971936 | snp | C/T | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118988 | AAATAATAATAATAA[C/T]AATATCTCTCTTATC | 25853 |
rs10971937 | snp | A/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120688 | AAAAAAAAAAAAAAA[A/G]AAAACAAAGCAACCC | 25853 |
rs10971938 | snp | C/T | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120722 | CATAATGGGTTAGCC[C/T]GATACTCTCAGGTAG | 25853 |
rs10971939 | snp | A/C | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123437 | TTTGCAGATGCAAAA[A/C]CAAAAGCACAAATAA | 25853 |
rs10971940 | snp | A/G | 0.171899 | 0.237487 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127213 | TGCCCAGCACAACCA[A/G]CCCAGGCCGCCCTAC | 25853 |
rs10971942 | snp | A/C | 0.479421 | 0.0993283 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127765 | AGTTACCTGCTGGTC[A/C]CTTCAGGCTTCAGGC | 25853 |
rs10971943 | snp | C/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128429 | CTAATTTTTTTTTTT[C/T]TTTTTTGAGACGGAG | 25853 |
rs11557154 | snp | A/G | 0.295771 | 0.245774 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107507 | CCATTCTGAAAGACC[A/G]GGAGCCTGGAGGTGT | 25853 |
rs11788468 | snp | C/T | 0.487007 | 0.100199 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115078 | AGGAAAGTAATTCTA[C/T]GCAGGTCACACAGAC | 25853 |
rs11790791 | snp | C/T | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119625 | TCCTTTGGATAAATT[C/T]TCAGGTGTGAACATT | 25853 |
rs11793082 | snp | C/T | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088703 | AACGTTAGAGAAGAA[C/T]GGAGCAGCTGAAGAA | 25853 |
rs11794829 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119854 | ccaaaggcacaagcc[A/C]ccatgcccagctaat | 25853 |
rs12002910 | snp | A/G | 0.29278 | 0.246313 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091466 | acatgatgagaacct[A/G]tctctacaaaaatac | 25853 |
rs12337902 | snp | C/T | 0.279991 | 0.248195 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105113 | gaaaaattagcctgg[C/T]gtggtggtgggcacc | 25853 |
rs12346581 | snp | A/G | 0.0733688 | 0.176922 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127721 | GGATGCTCTTGCTTG[A/G]GGCTGATTGGCCTCA | 25853 |
rs12347013 | snp | A/C | 0.293037 | 0.246268 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105132 | gtggtgggcacctgt[A/C]atcccagctactcag | 25853 |
rs12351094 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101092 | tttttttttaaatga[A/G]acaggttctggctct | 25853 |
rs12351200 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108808 | caaaaaaaataaata[A/T]ataaatatatatata | 25853 |