SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs10044 | snp | A/G | | | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075501 | CTAAAGCTCTGTAAA[A/G]AAAAAAATATAATAA | 55827 |
rs10693 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056108 | TGGTGCTTTGGAAAG[C/T]GTGAAAGCTGCTAGT | 55827 |
rs149912 | snp | A/T | 0.491629 | 0.0641526 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988565 | AAACTACTGTGCTCT[A/T]AATAATGTATGTCAG | 55827 |
rs169309 | snp | A/G | 0.197703 | 0.244469 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064031 | TGAGAAAGAGAGGGG[A/G]AAAAAAAAAAAAAAA | 55827 |
rs169310 | snp | A/C | 0.249038 | 0.249998 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034741 | AGGTTTAGAACTTCA[A/C]GTAAACACACAAATA | 55827 |
rs172088 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064076 | AAAAAAAAAAAATCC[A/C]CCAGAAACTTTTCAG | 55827 |
rs172113 | snp | A/G | 0.489837 | 0.0705577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011738 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGTG | 55827 |
rs175752 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977262 | gaaggaaagaaaagg[A/G]aaCTGAAATTGTTTT | 55827 |
rs175753 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977246 | aaCTGAAATTGTTTT[C/T]TATCAACAAACTCTC | 55827 |
rs175754 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977155 | gagctttgagaggca[A/G]aggcaggcagatcac | 55827 |
rs175755 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977141 | agaggcaggcagatc[A/C]cctgaggtcgggagt | 55827 |
rs175756 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977046 | ggagtggtggtatgc[A/C]cctataatcccagct | 55827 |
rs182141 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033075 | ACGAAATTATAATCA[C/T]GAGGTTCTAAAAGAT | 55827 |
rs183230 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040658 | CACGTCTTTTCCATT[C/T]TCATGTTTCTGTACA | 55827 |
rs185702 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977233 | TTCTATCAACAAACT[C/T]TCATGTAAAAAAAAA | 55827 |
rs188033 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977170 | atgcctgtaatccca[A/G]agctttgagaggcag | 55827 |
rs191847 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049763 | caggttcacgccatt[C/T]tcctgcctcagcctc | 55827 |
rs191852 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976988 | tgaacccaggaggca[A/G]aggttgtggtgagcc | 55827 |
rs201533 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047012 | AGGCTAATTATAACA[C/G]TTAATACCAAGCCTG | 55827 |
rs201534 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057598 | GTATCTAGCACATAA[C/T]AGGTTTATTGAAGTA | 55827 |
rs201535 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056893 | AGTGAAAAACTAAAG[A/G]GAAATAAAAGCTTCT | 55827 |
rs201536 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033606 | TTTCAggccgggcgc[A/G]gtggctcacacctgt | 55827 |
rs201537 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030352 | TAGTCATCCTGTATG[C/T]GGCATCTCAGAGGCT | 55827 |
rs201538 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027883 | GACAACCAGGGAGCT[A/G]CATTAATGAATGAAG | 55827 |
rs201539 | snp | C/T | 0.493748 | 0.0555599 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026169 | TGATTACAAATGTGA[C/T]AAATGCAATGAGGAA | 55827 |
rs201540 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023645 | AATAAGTAACGCGTT[C/T]ATTTCATCAGGCTCT | 55827 |
rs201541 | snp | A/T | 0.491157 | 0.065903 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023106 | GTGAGAGAGCTTAGT[A/T]TATGCATTGCAATAA | 55827 |
rs202238 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984258 | CAGAAGTGCTTCTTC[G/T]GTAACATTCTTACAC | 55827 |
rs202239 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984010 | ttactgttttttaca[A/C/G]ctaccatagtcgcaa | 55827 |
rs202240 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982741 | tctttctcaagtcca[A/G]tgtctagaatggcgt | 55827 |
rs202241 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965741 | aagcagttctcctgt[C/T]gggaggctgaggcct | 55827 |
rs202242 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965854 | tggtcaggctggtct[C/T]gaacctctgacatca | 55827 |
rs202243 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969403 | AGCTGGGATAACATA[C/T]GAGTTCTAATTAGGT | 55827 |
rs202244 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972874 | AAATTTTAATTAGTT[G/T]ATTTAATAAGGGAAT | 55827 |
rs202245 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971378 | ATCCTCAACACTTAA[C/T]ATTATTTATTTACCT | 55827 |
rs202246 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970731 | ACCATGAGTCAAATA[C/T]TACCTGTTTTTATAG | 55827 |
rs202247 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000918 | ttatataatgatgac[A/G]gttgtacctctttat | 55827 |
rs202248 | snp | A/G | 0.434253 | 0.168969 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002785 | TGGTAGTTGTTATCA[A/G]ATTAGTCTCCAAAAA | 55827 |
rs202249 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008208 | tcctaacctcaagca[G/T]tccatccgcctcggc | 55827 |
rs202250 | snp | C/G | 0.348574 | 0.229746 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008513 | TCTCCTAATTAATCT[C/G]CCTGTACCTACTGTT | 55827 |
rs202251 | snp | C/G | 0.378174 | 0.214642 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009452 | tctttctttctttct[C/G]tctctctctcttcct | 55827 |
rs202252 | snp | C/T | 0.314787 | 0.241459 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010980 | TATGATTTAGAGAAG[C/T]TGGTAACTTTGAAGT | 55827 |
rs202253 | snp | G/T | 0.476746 | 0.10529 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017227 | AATAAAACATTTTTG[G/T]TTTTTTTTTTGCTGT | 55827 |
rs202254 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018393 | TATTTTTGGTTGTTC[A/G]CTCTTTGTCATCAGT | 55827 |
rs202255 | snp | A/G | 0.429837 | 0.173662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019415 | CATATAAAGGCCCCC[A/G]TAAGGTTGATAGCAT | 55827 |
rs202256 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996008 | ataaggactatgttc[C/T]gtataagtagaacaa | 55827 |
rs202257 | snp | A/G | 0.488606 | 0.0746142 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995478 | TGAGGTCAGGAGTTC[A/G]AGACCAACCTGGCCA | 55827 |
rs202258 | snp | C/T | 0.491421 | 0.0649309 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995444 | TAGCACTTTGGGAGG[C/T]CGAGGCGAGTGGATC | 55827 |
rs202259 | snp | A/G | 0.489318 | 0.0722982 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992834 | AAGGATATTGCATAC[A/G]TTGCATACTAATGTA | 55827 |
rs202260 | snp | G/T | 0.485933 | 0.0826777 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986929 | AAAAAAGGtttttat[G/T]gtagtaaaatacata | 55827 |
rs202261 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985692 | tttgggctactatta[C/T]tctgcttaccacaAT | 55827 |
rs202262 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022012 | AGGGCTACAGTAAAA[C/G]AGAAACATAGGTAAT | 55827 |
rs202263 | snp | C/T | 0.432063 | 0.171327 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021844 | GGTATTTTAAGATTG[C/T]CCTTAGCTGGATAGC | 55827 |
rs202264 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021375 | AAAAATGTGACTCAC[A/G]GTGAAATAAATATTG | 55827 |
rs202265 | snp | C/G | 0.490563 | 0.0680388 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020993 | TCCTTTTTGGTTTTA[C/G]TCTGCCATAGACATT | 55827 |
rs202266 | snp | G/T | 0.489492 | 0.0717183 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960545 | ctgacctcgtgatct[G/T]cctgtcttggcctcc | 55827 |
rs202267 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959957 | tcatctgagtttttt[C/T]cctatgttatcttct | 55827 |
rs202268 | snp | A/G | 0.484421 | 0.0868729 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958101 | cactatgaggaaggc[A/G]aaaagacaacccata | 55827 |
rs202269 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957101 | aaattaaaaaaaaaA[A/T]AAATGTCCACTTATA | 55827 |
rs202270 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955730 | attccactccttcta[G/T]tcaatcttataatag | 55827 |
rs202271 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953719 | cccagctactcggga[A/G]gctgcagcggagaac | 55827 |
rs202272 | snp | A/G | 0.31721 | 0.240796 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953615 | agaccccatatcaaa[A/G]aaTAATAATAATAAT | 55827 |
rs202273 | snp | A/G | 0.484491 | 0.0866827 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950725 | GAAGGCTGAATTTAC[A/G]ACAAAGAACAATAAT | 55827 |
rs202274 | snp | C/G | 0.305934 | 0.243663 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950253 | TCTCATTGAGTTATA[C/G]GAGTTAAGAAACAAA | 55827 |
rs203248 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963324 | tcaaagggattactg[G/T]tatagttggattaat | 55827 |
rs203255 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980200 | taaataaataaataa[A/G]taaataaataaattc | 55827 |
rs203787 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936547 | AGATGACGACCACCC[C/T]GGGGACTGAGGCTGG | 55827 |
rs203788 | snp | G/T | 0 | 0 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937001 | CCGCTCACCCAGGTA[G/T]CGACTCCGCAGCCGG | 55827 |
rs203789 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940382 | CTCACCCTGCCCCCC[A/G]CCTCCCACCAAAAAA | 55827 |
rs203790 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941485 | CACAGGTTGCCACAT[A/G]AATGTACTTTTATCA | 55827 |
rs203791 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943661 | atgaggaggtgggag[C/G]atgatgagaaattcg | 55827 |
rs203792 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945861 | tgatttggttttcat[C/T]ttgaatcattattgg | 55827 |
rs369851 | snp | C/G | 0.249603 | 0.25 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065228 | AATAGAAAATCCCCC[C/G]TAAGAAGAGGGACTT | 55827 |
rs369914 | snp | A/T | 0.203267 | 0.245593 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065018 | GAAATAATTCACAGA[A/T]AAAAGAAATTGTCTT | 55827 |
rs370952 | snp | C/T | 0.249603 | 0.25 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065525 | CAAAGATTTATGCTA[C/T]TCTTACATTTTTTTA | 55827 |
rs380095 | snp | C/G | 0.178144 | 0.239451 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065866 | CTATCTGACTAGGCA[C/G]CAGTAGAGTCAATTA | 55827 |
rs380682 | snp | C/T | 0.236724 | 0.249647 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037104 | GAGATTCTCCCCCCC[C/T]TTTTTTTTTTTTTTT | 55827 |
rs380753 | snp | G/T | 0.4582 | 0.138394 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066035 | ATTGTATATCCAAAT[G/T]GAACATCCAGTCATT | 55827 |
rs381095 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054052 | AGTATCTGAAATAAG[C/T]GAGGGAGATGGGTTG | 55827 |
rs399096 | snp | A/G | 0.000447616 | 0.0149535 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065787 | TGACTGATGAGTCAT[A/G]CAAATAATTTCTAGC | 55827 |
rs399273 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067497 | GCTCCCTGTCTGCCT[A/G]GTGAACTATTCTCAG | 55827 |
rs410215 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052974 | TCCAAGTATGGCAAT[A/G]TAGACAGCATGACCA | 55827 |
rs413168 | snp | C/G | 0.492137 | 0.0622048 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036551 | TCTGTTTCATCTATT[C/G]CAGAAGCCTAAAGAC | 55827 |
rs417427 | snp | G/T | 0.288646 | 0.246995 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045294 | TTTGTTTGAAGTCAT[G/T]GAAGGGAATCTCTCC | 55827 |
rs428694 | snp | C/G | 0.434109 | 0.169127 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002742 | AGAAGTGGAATGGCG[C/G]AGTCACTGGATAAGT | 55827 |
rs430565 | snp | C/T | 0.211516 | 0.24702 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055006 | tatttttagtagaga[C/T]ggggtttTTAACTTG | 55827 |
rs433173 | snp | G/T | 0.288646 | 0.246995 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045295 | TTGTTTGAAGTCATT[G/T]AAGGGAATCTCTCCA | 55827 |
rs433385 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990425 | GACAGTATGAGAGAT[C/T]TGTCATAGGTAGATT | 55827 |
rs435486 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072295 | AGGGAGAATCAGTCT[A/T]AAAAAAAAAAAAAAA | 55827 |
rs435847 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049549 | ctataggcgtgagcc[A/C]ccgcgcctggccATA | 55827 |
rs436256 | snp | G/T | 0.434687 | 0.168495 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002741 | TAGAAGTGGAATGGC[G/T]CAGTCACTGGATAAG | 55827 |
rs438806 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041894 | ATACATGTTTGTCGC[A/G]CACACACACACACAC | 55827 |
rs445995 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002045 | TAAATTGTCAATAAT[A/G]AGTAAATTGTCAATA | 55827 |
rs463206 | snp | C/T | 0.00350262 | 0.0417018 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953001 | ATATCTTCAGCAAGG[C/T]GGATCTTCAGCAAGG | 55827 |
rs593632 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049363 | ttttcccccttcagt[C/T]tcccaagtagctggg | 55827 |
rs598535 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071092 | gatcaAGGGTATATA[A/C]ATATTAGGTCTATTC | 55827 |
rs624006 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049357 | aagcgatcttcctcc[C/T]tcagtctcccaagta | 55827 |
rs671608 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938272 | TCTCATACACACACA[A/C]ACACACACACACCCC | 55827 |
rs675686 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050046 | AGTAATTTAGGTTTT[C/T]TTTTGAGTTTAGAAA | 55827 |
rs675689 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050044 | TAATTTAGGTTTTTT[C/T]TTGAGTTTAGAAACA | 55827 |