SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs935888 | snp | G/T | 0.274393 | 0.248807 | upstream-variant-2KB | TRIM69 | GRCh38.p7 | 15:44735829 | GAGATAATGACGGGG[G/T]TGTGGGGGAAGGGAA | 140691 |
rs935889 | snp | G/T | 0.274393 | 0.248807 | upstream-variant-2KB | TRIM69 | GRCh38.p7 | 15:44736153 | GGTGTTTCCCAGGCC[G/T]GTGTTACTGTCTCAG | 140691 |
rs1901534 | snp | C/G | 0.403334 | 0.197456 | | | GRCh38.p7 | 15:44753351 | TGTTGTtcctgggct[C/G]aaatgatctgcccac | 140691 |
rs1901535 | snp | A/G | 0.420733 | 0.18262 | | | GRCh38.p7 | 15:44754272 | GCTAGGATTACAGGC[A/G]CCTGCCACCACACCC | 140691 |
rs1901536 | snp | C/T | 0.0637235 | 0.166737 | | | GRCh38.p7 | 15:44757204 | AGTGTGAGCATTCat[C/T]cattcatttaacaaa | 140691 |
rs1901537 | snp | C/T | 0.402982 | 0.197728 | | | GRCh38.p7 | 15:44757252 | AGGCATAATACTAGA[C/T]ATTGGGGATGGGAGA | 140691 |
rs1901538 | snp | A/C | 0.242775 | 0.249896 | intron-variant | TRIM69 | GRCh38.p7 | 15:44757330 | TGATAAGTACTATAA[A/C]TGAAAGTATAGGGTA | 140691 |
rs2084835 | snp | C/T | 0.33303 | 0.235809 | intron-variant | TRIM69 | GRCh38.p7 | 15:44757497 | tagcctggagaagaa[C/T]gttctaggaatagaa | 140691 |
rs2123149 | snp | C/G | 0.420574 | 0.182769 | intron-variant | TRIM69 | GRCh38.p7 | 15:44756818 | AAAGATTGCTATGTC[C/G]AAAGAAATACCTTTA | 140691 |
rs2290331 | snp | A/G | 0.405776 | 0.195535 | intron-variant | TRIM69 | GRCh38.p7 | 15:44758395 | CTGCAATAGGAAACT[A/G]GAGGTCACTTTTGCC | 140691 |
rs2412918 | snp | C/T | 0.353587 | 0.22753 | intron-variant | TRIM69 | GRCh38.p7 | 15:44740521 | ctagaataaccaata[C/T]agagaagtgcttaaa | 140691 |
rs2444001 | snp | A/G | | | upstream-variant-2KB | TRIM69 | GRCh38.p7 | 15:44735420 | agaGgaaagaaggaa[A/G]gaaggaaggaaggaa | 140691 |
rs2444002 | snp | A/C | 0.249038 | 0.249998 | intron-variant | TRIM69 | GRCh38.p7 | 15:44739982 | ctgggaggcaccccc[A/C]agtaggggcagactg | 140691 |
rs2444003 | snp | A/G | 0.404559 | 0.196498 | intron-variant | TRIM69 | GRCh38.p7 | 15:44747650 | AAAGAGAAGATGGCC[A/G]TATTAGGTCCAGACA | 140691 |
rs2444004 | snp | G/T | 0.266819 | 0.249434 | intron-variant | TRIM69 | GRCh38.p7 | 15:44748314 | TGTGAGCAGCTCTTG[G/T]GCAGAGCCTCTATGT | 140691 |
rs2444005 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | TRIM69 | GRCh38.p7 | 15:44751714 | ttagcactattttca[C/T]tgtatcccataagtt | 140691 |
rs2444006 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | TRIM69 | GRCh38.p7 | 15:44751774 | tttttgagacagggt[C/T]ttgttttgtcaccca | 140691 |
rs2444007 | snp | A/G | 0.0151753 | 0.085775 | intron-variant, missense | TRIM69 | GRCh38.p7 | 15:44754927 | CCCTCCTCCAACATC[A/G]ATCCAGGCGACTATG | 140691 |
rs2444008 | snp | A/T | 0 | 0 | intron-variant | TRIM69 | GRCh38.p7 | 15:44762301 | CTTGCTTTTTGTCAC[A/T]TGCTTCCATCAATTT | 140691 |
rs2444009 | snp | A/G | 0.394721 | 0.203852 | intron-variant | TRIM69 | GRCh38.p7 | 15:44762754 | catgccttcctctac[A/G]ttcttgaaaaaatgg | 140691 |
rs2468062 | snp | A/G | 0.402806 | 0.197864 | intron-variant | TRIM69 | GRCh38.p7 | 15:44751537 | tggctcatgcctgta[A/G]tcccagcattttggg | 140691 |
rs2468063 | snp | A/T | 0.5 | 0 | intron-variant | TRIM69 | GRCh38.p7 | 15:44750710 | aaaaaaaaaagaaaa[A/T]gtaatgaaataaaaa | 140691 |
rs2468064 | snp | C/T | 0.404733 | 0.196361 | intron-variant | TRIM69 | GRCh38.p7 | 15:44744719 | ctgctcccacttgta[C/T]tatgtacctgtagtt | 140691 |
rs2468065 | snp | C/T | 0.404733 | 0.196361 | intron-variant | TRIM69 | GRCh38.p7 | 15:44744675 | tctttaaaaccacca[C/T]caagatgggaaatga | 140691 |
rs2468066 | snp | A/G | 0.248755 | 0.249997 | intron-variant | TRIM69 | GRCh38.p7 | 15:44739912 | ggaggcagtctgccc[A/G]ttctcagatctccag | 140691 |
rs2468067 | snp | G/T | 0.274661 | 0.248781 | intron-variant | TRIM69 | GRCh38.p7 | 15:44739149 | taatgggtatggaat[G/T]tcttttggggataat | 140691 |
rs2468068 | snp | A/G | | | intron-variant | TRIM69 | GRCh38.p7 | 15:44736721 | AGTTAAAAAAAAAAA[A/G]GGTCACTCACCTCCA | 140691 |
rs2468071 | snp | C/T | 0.490287 | 0.0690083 | intron-variant | TRIM69 | GRCh38.p7 | 15:44763054 | ttaacaactaatgaa[C/T]caaattgatacatta | 140691 |
rs2470908 | snp | C/T | 0.24932 | 0.249999 | utr-variant-5-prime | TRIM69 | GRCh38.p7 | 15:44736512 | AGTTAACTGACAAAC[C/T]GTCACGGAATCTGCC | 140691 |
rs2470911 | snp | A/G | 0.44621 | 0.154924 | intron-variant, missense | TRIM69 | GRCh38.p7 | 15:44754936 | AACATCGATCCAGGC[A/G]ACTATGTTGAAATGA | 140691 |
rs2470913 | snp | A/T | 0.247053 | 0.249983 | intron-variant | TRIM69 | GRCh38.p7 | 15:44738236 | GCTAATTTTTGTATT[A/T]TTATTTTTTTTTTTA | 140691 |
rs2899122 | snp | G/T | 0.337614 | 0.234145 | intron-variant | TRIM69 | GRCh38.p7 | 15:44750905 | gattttttatctttt[G/T]agtagattgtttttc | 140691 |
rs2960206 | snp | C/T | 0.27893 | 0.24832 | intron-variant | TRIM69 | GRCh38.p7 | 15:44739558 | gacgggcttaaagaa[C/T]ggtgcaccaggagat | 140691 |
rs3100139 | snp | C/T | 0.320259 | 0.239924 | intron-variant, missense | TRIM69 | GRCh38.p7 | 15:44755375 | CTGTCCATTTCTTCA[C/T]GGTGGGTGAGCCCTG | 140691 |
rs3100140 | snp | C/T | 0.240765 | 0.249829 | intron-variant | TRIM69 | GRCh38.p7 | 15:44760403 | AAGGACTGAGCAAGA[C/T]AAAATAACACACATG | 140691 |
rs3100141 | snp | C/T | 0.272241 | 0.249009 | intron-variant | TRIM69 | GRCh38.p7 | 15:44763934 | tttttccattctggt[C/T]ggcaagattgaaaat | 140691 |
rs3100142 | snp | A/T | 0.41141 | 0.19091 | intron-variant | TRIM69 | GRCh38.p7 | 15:44764699 | acctgttggttgtag[A/T]ttgcctactcTAGCT | 140691 |
rs3100143 | snp | A/T | 0.233922 | 0.249489 | utr-variant-3-prime | TRIM69 | GRCh38.p7 | 15:44767816 | TGTTATTAAAGAGGT[A/T]TTGAAATATTTTACC | 140691 |
rs3100144 | snp | C/T | 0.0640965 | 0.167152 | downstream-variant-500B | TRIM69 | GRCh38.p7 | 15:44767853 | ACTGGATTCTCTTCT[C/T]AATTTTTGGGGAACT | 140691 |
rs3110172 | snp | C/T | 0.420255 | 0.183066 | intron-variant | TRIM69 | GRCh38.p7 | 15:44752835 | taattcaccctagat[C/T]gttataaagttgact | 140691 |
rs3110173 | snp | C/T | 0.403684 | 0.197183 | intron-variant | TRIM69 | GRCh38.p7 | 15:44752737 | agaatcaaaatgtta[C/T]gctagaaaaaaatca | 140691 |
rs3110174 | snp | A/T | 0.404384 | 0.196635 | intron-variant | TRIM69 | GRCh38.p7 | 15:44749768 | caaaaaactaccata[A/T]gacagacctaccaat | 140691 |
rs3110175 | snp | A/G | 0.234692 | 0.249531 | intron-variant | TRIM69 | GRCh38.p7 | 15:44749003 | atcccggctactcgg[A/G]aggctgaggctggag | 140691 |
rs3110176 | snp | C/T | 0.404559 | 0.196498 | intron-variant | TRIM69 | GRCh38.p7 | 15:44748597 | CCTCAAGTGATCCAC[C/T]CACCTTGGCCTCCCA | 140691 |
rs3110177 | snp | A/G | 0.279195 | 0.248289 | intron-variant | TRIM69 | GRCh38.p7 | 15:44739421 | gtgaggcaatgcctc[A/G]ccctgcttcggctca | 140691 |
rs3110183 | snp | C/T | 0.459347 | 0.136653 | intron-variant | TRIM69 | GRCh38.p7 | 15:44765239 | GACAAAAAGCTGACT[C/T]ATGGGAATCTTCAGA | 140691 |
rs3110662 | snp | C/G | 0.419616 | 0.183658 | intron-variant | TRIM69 | GRCh38.p7 | 15:44747265 | AGGTAGAATGGAGGA[C/G]AGAGACTCTGCATTG | 140691 |
rs3110673 | snp | C/T | 0.084728 | 0.187577 | intron-variant | TRIM69 | GRCh38.p7 | 15:44764398 | GACCTTTGTAAAATA[C/T]ATTCCATACTTTTTA | 140691 |
rs3110674 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | TRIM69 | GRCh38.p7 | 15:44766823 | GCACTTTGAGAGGCC[C/T]AGGCAGGTGGGTTGC | 140691 |
rs3110677 | snp | G/T | 0.248188 | 0.249993 | upstream-variant-2KB | TRIM69 | GRCh38.p7 | 15:44735140 | aatcctagcactttg[G/T]gaggctgaggtggga | 140691 |
rs3110681 | snp | A/G | 0 | 0 | intron-variant | TRIM69 | GRCh38.p7 | 15:44744386 | GGGTGCAGCACACCA[A/G]CATGGCACATGTATA | 140691 |
rs3759878 | snp | C/T | 0.207559 | 0.246371 | utr-variant-5-prime | TRIM69 | GRCh38.p7 | 15:44736389 | ACCTTAAGATTAGAC[C/T]ACTAACTCGAATCTA | 140691 |
rs3759880 | snp | C/T | 0.213757 | 0.247359 | utr-variant-5-prime, missense | TRIM69 | GRCh38.p7 | 15:44756453 | AGAAGGAAGCTATTG[C/T]TGCTCACAAGGTGAG | 140691 |
rs3759881 | snp | A/T | 0.172674 | 0.237741 | intron-variant | TRIM69 | GRCh38.p7 | 15:44756559 | CTAACATATATTATC[A/T]ACACACTAAATGGTA | 140691 |
rs3759882 | snp | A/G | 0.138886 | 0.22395 | intron-variant | TRIM69 | GRCh38.p7 | 15:44756585 | TGGTACCTAGGCTAT[A/G]GAATTGGAAAACTGA | 140691 |
rs3759883 | snp | A/G | 0.138886 | 0.22395 | intron-variant | TRIM69 | GRCh38.p7 | 15:44756643 | GTGGAGTAGGTTCCT[A/G]ATAGCTGATCAACAG | 140691 |
rs3759884 | snp | C/G | 0.138886 | 0.22395 | intron-variant | TRIM69 | GRCh38.p7 | 15:44756811 | AATCACTAAAGATTG[C/G]TATGTCCAAAGAAAT | 140691 |
rs3837719 | in-del | -/A | 0 | 0 | intron-variant | TRIM69 | GRCh38.p7 | 15:44756773 | ATGGCAAAAAAAAAA[-/A]GGAACTTATTAGAAA | 140691 |
rs3959609 | snp | C/T | | | intron-variant | TRIM69 | GRCh38.p7 | 15:44744836 | ttaactcagaacttt[C/T]tcacagatgagatgg | 140691 |
rs3986133 | in-del | -/GA | | | intron-variant | TRIM69 | GRCh38.p7 | 15:44747255 | TCTGTTGCTGAGGTA[-/GA]ATGGAGGAGAGAGAC | 140691 |
rs4386112 | snp | A/G | 0.248471 | 0.249995 | intron-variant | TRIM69 | GRCh38.p7 | 15:44746008 | gaaatttgacaaaag[A/G]cataaagctatacat | 140691 |
rs4505283 | snp | G/T | 0.235564 | 0.249583 | intron-variant | TRIM69 | GRCh38.p7 | 15:44745522 | gaacatatggcccat[G/T]gacaggagaaaagga | 140691 |
rs4536441 | snp | C/T | 0.404384 | 0.196635 | intron-variant | TRIM69 | GRCh38.p7 | 15:44750657 | cagtctacttaatgg[C/T]ttctaaattttgtgg | 140691 |
rs4923993 | snp | C/T | 0.207864 | 0.246424 | upstream-variant-2KB | TRIM69 | GRCh38.p7 | 15:44734702 | TCTTAGCTAAGGCTA[C/T]TCAGTGCTCTGGTGG | 140691 |
rs6416440 | snp | G/T | 0.193028 | 0.243422 | intron-variant | TRIM69 | GRCh38.p7 | 15:44749226 | aaaattgaggtaaaa[G/T]tcatacaacataaaa | 140691 |
rs6493116 | snp | A/G | 0.248188 | 0.249993 | upstream-variant-2KB | TRIM69 | GRCh38.p7 | 15:44735173 | acagcttgagctcag[A/G]aatttgagatcagcc | 140691 |
rs6493117 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | TRIM69 | GRCh38.p7 | 15:44735460 | gaaggaaggaaggaa[A/G]gaaggaaggaaggaa | 140691 |
rs6493118 | snp | C/T | 0.168785 | 0.236441 | intron-variant | TRIM69 | GRCh38.p7 | 15:44738365 | AGGCCTGGGCCATCG[C/T]GACCTGCTGATGTGC | 140691 |
rs6493119 | snp | A/G | 0.27893 | 0.24832 | intron-variant | TRIM69 | GRCh38.p7 | 15:44739205 | cctgccttggtaacc[A/G]ctatatattttAAAC | 140691 |
rs6493120 | snp | A/C | 0.0998734 | 0.199905 | intron-variant | TRIM69 | GRCh38.p7 | 15:44740423 | aggcttcagatgatc[A/C]aactactccgagcta | 140691 |
rs6493121 | snp | A/C | 0.251014 | 0.249998 | intron-variant | TRIM69 | GRCh38.p7 | 15:44740632 | gaagatctaccaagc[A/C]aatggaaaacaaaaa | 140691 |
rs6493123 | snp | A/C | 0.17332 | 0.23795 | intron-variant | TRIM69 | GRCh38.p7 | 15:44750709 | atttttatttcatta[A/C]tttttcttttttttt | 140691 |
rs6493124 | snp | A/G | 0.204496 | 0.245824 | intron-variant | TRIM69 | GRCh38.p7 | 15:44752667 | attttgttattttct[A/G]tatgtgcttttttgt | 140691 |
rs6493125 | snp | C/T | 0.234692 | 0.249531 | intron-variant | TRIM69 | GRCh38.p7 | 15:44752721 | cttttttgtgattaa[C/T]tgatttttttctagc | 140691 |
rs6493126 | snp | G/T | 0.20111 | 0.245173 | intron-variant | TRIM69 | GRCh38.p7 | 15:44765621 | CAGCTGAGCGTGGTG[G/T]TGCATGCCTGTAATC | 140691 |
rs6493127 | snp | C/T | 0.121971 | 0.214729 | intron-variant | TRIM69 | GRCh38.p7 | 15:44767192 | TTTGTGTTTACCCCC[C/T]TTTCTCCCATGCTCT | 140691 |
rs7162713 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | TRIM69 | GRCh38.p7 | 15:44735854 | AGGGAAACTCCCATC[C/T]GAAGGGACAACATAT | 140691 |
rs7164679 | snp | G/T | 0.244205 | 0.249933 | intron-variant | TRIM69 | GRCh38.p7 | 15:44753540 | tactgagaatccctt[G/T]tatgtgaagagtcat | 140691 |
rs7166053 | snp | A/T | 0.243061 | 0.249904 | intron-variant | TRIM69 | GRCh38.p7 | 15:44753722 | ttactttttcaaaaa[A/T]ttttttttttgagac | 140691 |
rs7166101 | snp | C/T | 0.242201 | 0.249878 | intron-variant | TRIM69 | GRCh38.p7 | 15:44753781 | ggtgcagtggagtga[C/T]ctcagcttactataa | 140691 |
rs7167254 | snp | G/T | 0.154993 | 0.231244 | intron-variant | TRIM69 | GRCh38.p7 | 15:44757341 | ATAACTGAAAGTATA[G/T]GGTATGATGATAGCA | 140691 |
rs7168751 | snp | A/G | 0.235273 | 0.249566 | intron-variant | TRIM69 | GRCh38.p7 | 15:44751117 | catgcaccacaccta[A/G]cttttttttttcttt | 140691 |
rs7169341 | snp | A/T | 0.173643 | 0.238054 | intron-variant | TRIM69 | GRCh38.p7 | 15:44738239 | AATTTTTGTATTATT[A/T]TTTTTTTTTTTAGTA | 140691 |
rs7169922 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM69 | GRCh38.p7 | 15:44760099 | ATATCAGGATTACTT[C/T]TTAGCATATGATTTT | 140691 |
rs7177200 | snp | C/T | | | intron-variant | TRIM69 | GRCh38.p7 | 15:44738058 | TTTCtttctttcttt[C/T]ttttttttttttttt | 140691 |
rs7177509 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | TRIM69 | GRCh38.p7 | 15:44755611 | CTGTACCTAAACTCT[G/T]CCATGGTAGCACTCT | 140691 |
rs7177746 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | TRIM69 | GRCh38.p7 | 15:44755741 | TATTAAGATAGCCTC[C/G]TGTTAAAAGTTAAAT | 140691 |
rs7178434 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | TRIM69 | GRCh38.p7 | 15:44749013 | agccttccgagtagc[C/T]gggattacaggcacg | 140691 |
rs7178712 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | TRIM69 | GRCh38.p7 | 15:44740078 | cgcggttcacgaaaa[C/T]ccactgttctgcagc | 140691 |
rs7182388 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | TRIM69 | GRCh38.p7 | 15:44752903 | ttactataaaaactc[C/T]gctccttttcagctc | 140691 |
rs7182487 | snp | A/G | 0.241627 | 0.24986 | intron-variant | TRIM69 | GRCh38.p7 | 15:44756219 | TTTCACAATTCTTGA[A/G]CGAGACAAGAACTAT | 140691 |
rs7182564 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | TRIM69 | GRCh38.p7 | 15:44740344 | ttcctccaaaggaac[A/G]cagttcctcaccagc | 140691 |
rs7182597 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | TRIM69 | GRCh38.p7 | 15:44753062 | ccaaaaactgcaata[C/T]tggactttacctatg | 140691 |
rs7183362 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | TRIM69 | GRCh38.p7 | 15:44740209 | caaacagaaaggaca[C/T]ccataccaaaaaccc | 140691 |
rs7497862 | snp | A/G | 0.168785 | 0.236441 | intron-variant | TRIM69 | GRCh38.p7 | 15:44762029 | gctggagtgtggtgc[A/G]atctcggctcactgc | 140691 |
rs8026572 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM69 | GRCh38.p7 | 15:44744996 | agttattttggggaa[C/T]accctttgaaaagta | 140691 |
rs8031964 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | TRIM69 | GRCh38.p7 | 15:44760155 | GCCAAAATTTTATCT[C/T]GTTTTGCTAAATCAG | 140691 |
rs8033099 | snp | C/T | 0.106633 | 0.204807 | intron-variant | TRIM69 | GRCh38.p7 | 15:44739112 | tacaattatcaccac[C/T]atctaattccagaac | 140691 |
rs8036450 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | TRIM69 | GRCh38.p7 | 15:44739299 | gctcccagcgtgagc[A/G]atgcagaagacgggt | 140691 |
rs8037029 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | TRIM69 | GRCh38.p7 | 15:44748386 | AGCTGCCATCACTGA[A/G]TGTTTATTTACACCA | 140691 |