SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7328 | snp | C/T | 0.358303 | 0.225323 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887728 | TGAAAGAGGAGACCC[C/T]TCTCTCTCTACTCTT | 25929 |
rs15287 | snp | A/T | 0 | 0 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887754 | TTTCaaattaaatat[A/T]ataaaaacaattaaa | 25929 |
rs168356 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924846 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 25929 |
rs180902 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913671 | aaaatacaaaaatta[A/G]ccgggtgtggtggtg | 25929 |
rs180903 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913873 | gggcatggtggtatg[C/T]gcctgtagtcccaac | 25929 |
rs193232 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913681 | aattagccgggtgtg[G/T]tggtgcacacctgta | 25929 |
rs348735 | snp | A/C | 0.431029 | 0.17242 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917235 | CAAATTACAAGTTAC[A/C]ATGCAAATAGTAGCT | 25929 |
rs348736 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917571 | TCAATGGCTGAATTA[G/T]GACTGTGTTACTATG | 25929 |
rs348737 | snp | A/G | 0.135208 | 0.222087 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918248 | TACTAAATGTTTACA[A/G]TGCTTAACCTTGTGA | 25929 |
rs348738 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918549 | AGCTCAGACTCCTAG[C/T]ATGAACCTCTGATCC | 25929 |
rs348739 | snp | A/C | 0.233185 | 0.249445 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154921380 | TGGCCCCCAGGCTAA[A/C]GTATATACAGTCTTC | 25929 |
rs348740 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922180 | ATTTTCTTTTTTTCT[G/T]TTTTAGAGACGGAGT | 25929 |
rs348741 | snp | A/G | 0.43221 | 0.171171 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922414 | cctcgtgatctgccc[A/G]cgtcggcctcccaaa | 25929 |
rs348749 | snp | A/T | 0.301681 | 0.2446 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937499 | TAGATGTGGCCAGAA[A/T]AAATCACCTGGCATG | 25929 |
rs348754 | snp | C/T | 0.302184 | 0.244493 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922985 | acaggcgtgagccac[C/T]gtgccaggccTTAAA | 25929 |
rs348755 | snp | C/G | 0.126606 | 0.217426 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924049 | ctcagcccactgaaa[C/G]tattatttaaaatgt | 25929 |
rs348756 | snp | A/T | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924902 | GCTGAGGCAGGAGAA[A/T]GGCGTGAACCCGGGA | 25929 |
rs348757 | snp | A/C | 0.289683 | 0.24683 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924909 | CAGGAGAAAGGCGTG[A/C]ACCCGGGAGGCGGAG | 25929 |
rs348758 | snp | G/T | 0.108103 | 0.205828 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154925577 | ATGCCATTCCAACAT[G/T]TGGTTATCTTATAAC | 25929 |
rs702743 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154891831 | GGGTCTGCTTCTTGG[G/T]TGATAAGAAATAGAA | 25929 |
rs816734 | snp | A/G | 0.497695 | 0.0338674 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893387 | ctgtcacccaggctc[A/G]ggtgtagtggcttac | 25929 |
rs816735 | snp | C/G | 0.299411 | 0.245069 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893329 | aattcttccgcctca[C/G]cctcccaagtagctg | 25929 |
rs816736 | snp | C/T | 0.0557983 | 0.157435 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154892388 | AGCCTTTCTCCCTGA[C/T]GGTAAGTGACTTCCT | 25929 |
rs816737 | snp | C/T | 0.093417 | 0.194889 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890936 | aaaccccgtctctac[C/T]aaaaattagctgggt | 25929 |
rs816738 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890087 | GGAACCCTTGTGCCT[A/G]TTGGTGGGAATGTAA | 25929 |
rs816739 | snp | A/G | 0.0561708 | 0.157893 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154889342 | AAATCAGAGAATGGC[A/G]AAATTTCCTGAGAGC | 25929 |
rs816740 | snp | A/G | 0.0561487 | 0.157866 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899328 | CAGATTGGCTAAAGG[A/G]TCTGTTCTTGCCTTT | 25929 |
rs816741 | snp | G/T | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897979 | CCGGAAGGCGGAGGT[G/T]GCAGCGAGCCAAGAT | 25929 |
rs816742 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897724 | CAGATGCAGCAGATC[A/G]CTTGAGATTAGGAGT | 25929 |
rs816743 | snp | C/T | 0.301932 | 0.244547 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897465 | TGGAAATCTCTTTAT[C/T]TCTTAAATTTTTTTG | 25929 |
rs816744 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897177 | GAATAAAAATGGAGG[C/T]GAAAATAGGACACCC | 25929 |
rs816745 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897113 | ATGACCAAGTCTAGA[A/G]AGATTTTAATTTATC | 25929 |
rs816746 | snp | C/T | 0.110907 | 0.207733 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896501 | ATCGCCCCTTTTGTC[C/T]CTTTTCATGCATGAC | 25929 |
rs816747 | snp | C/T | 0.498547 | 0.0269177 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896402 | ACACGGGAGAGCTCT[C/T]GAGATCATCCAGTGC | 25929 |
rs816748 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895132 | ATACTTTGAAAAACA[A/G]TTGGACAGTTTCTTT | 25929 |
rs816749 | snp | G/T | 0.0881222 | 0.190983 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894519 | cctcccaaagtgctg[G/T]gattacaagtgtgag | 25929 |
rs863650 | snp | C/T | 0.078151 | 0.181571 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901656 | ATCAAACAATTGATG[C/T]TTCAGAATGTGTAGA | 25929 |
rs888694 | snp | G/T | 0.289424 | 0.246872 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927925 | CAGCTCACTGCAGCC[G/T]CAACCTCCTGGGCTC | 25929 |
rs903837 | snp | C/T | 0.373196 | 0.217538 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928303 | AGTGATTCTGAAATT[C/T]AGTTCTGACTTCAGA | 25929 |
rs1035368 | snp | C/T | 0.333491 | 0.235646 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928747 | AACAAGCTTTTACAG[C/T]GCAGACTGTGTGTTA | 25929 |
rs1046337 | snp | A/C | 0 | 0 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887594 | TTATTTGAACAGATC[A/C]CTTACTAAAGCTTTA | 25929 |
rs1061755 | snp | A/C | | | upstream-variant-2KB | MRPL22, GEMIN5 | GRCh38.p7 | 5:154939341 | ACCTGGAACTGTTTA[A/C]TTTCCTGTAACCATT | 25929 |
rs1421813 | snp | C/T | 0.174423 | 0.238303 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154902675 | TTCTAAGTGACCTTT[C/T]CCTGTTTGAAAGAGA | 25929 |
rs1421814 | snp | C/G | 0.165501 | 0.235287 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902683 | GACCTTTTCCTGTTT[C/G]AAAGAGAGATAATGT | 25929 |
rs1421815 | snp | A/C | 0.195214 | 0.243923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902847 | TGAAGCCCACTTGGT[A/C]ACTGTACACTCCCAC | 25929 |
rs1974776 | snp | C/T | 0.222813 | 0.248517 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911936 | AAACAATAGAATAAC[C/T]AGAAAATGTCTTTTC | 25929 |
rs1974777 | snp | A/G | 0.223487 | 0.24859 | missense | GEMIN5 | GRCh38.p7 | 5:154911849 | ATTTCCGAGGACATC[A/G]AGGTCGACTGCTTTG | 25929 |
rs2042168 | snp | A/G | 0.302686 | 0.244385 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906246 | CACTATGGGAGGCCA[A/G]GGAAAGAGACTTGCT | 25929 |
rs2047305 | snp | A/T | 0.468349 | 0.121752 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933688 | CAGCTTTATTTATTT[A/T]TTTTTTTTAAAAGAA | 25929 |
rs2059045 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910479 | catttctaccaagaa[C/T]tgcaaaataaaagca | 25929 |
rs2112222 | snp | C/T | 0.084364 | 0.187256 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933769 | AGCTTGATCTGTTGG[C/T]GATTAGGTTGCATAA | 25929 |
rs2112223 | snp | C/T | 0.289424 | 0.246872 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929415 | TCCCCACCCACAGCA[C/T]GTTCACTGCCAAATT | 25929 |
rs2161128 | snp | C/G | 0.302686 | 0.244385 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933864 | GATAGAGAGGATGAA[C/G]AGAAAGGTGGTAGGC | 25929 |
rs2258437 | snp | C/T | 0.223481 | 0.24859 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154927412 | TGATGTAGAAAGTAA[C/T]AGCTGTTTGTCATCC | 25929 |
rs2270622 | snp | A/G/T | 0.024134 | 0.107647 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920190 | ACCATACCATACTAC[A/G/T]TAGTTGTTTTAAAAG | 25929 |
rs2544863 | snp | A/G | | | | | GRCh38.p7 | 5:154893254 | tttttttttttttta[A/G]agacgggctttcacc | 25929 |
rs2544866 | snp | A/G | 0.301932 | 0.244547 | | | GRCh38.p7 | 5:154932016 | CATTTTTTATTTATT[A/G]TTTATTTTTGGAGAC | 25929 |
rs2544870 | snp | C/T | 0.0325976 | 0.123435 | | | GRCh38.p7 | 5:154913437 | tgtataatttgaata[C/T]agtcatgagaaaata | 25929 |
rs2644742 | snp | C/G | 0.493013 | 0.058691 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914202 | ATTTTTGTATTTTTA[C/G]TAGAGACAGGGTTTC | 25929 |
rs2644743 | snp | C/T | 0.333491 | 0.235646 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928722 | CATGCATGAAGTCAC[C/T]GGTGGTTCATAACAC | 25929 |
rs2644744 | snp | C/T | 0.289683 | 0.24683 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931675 | AACTTAGCTATCTCT[C/T]TCATAGGTCTGAACT | 25929 |
rs2644745 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934293 | ctgggttcaagtgat[C/T]ctcctgcctcagcct | 25929 |
rs2688185 | snp | A/T | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903671 | TCTTTTGAATTTTTG[A/T]ACTGTTTTGTCTGTA | 25929 |
rs3749672 | snp | C/T | 0.000230624 | 0.0107359 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154932166 | CCATGATGATGAAAT[C/T]CACTCCATAGCCTGG | 25929 |
rs4354100 | snp | C/T | 0.299411 | 0.245069 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911032 | cagttgtcccagatt[C/T]ggtcagtgggaacct | 25929 |
rs4958393 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908608 | tttgactttcataat[C/T]tgaaacttctgaaga | 25929 |
rs4958769 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907078 | TGAGAGCCATCACTA[C/T]AGCTTAACTCACTAG | 25929 |
rs4958770 | snp | A/C | 0.0964687 | 0.197302 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907309 | CTATGTACACAACTG[A/C]CCCAGCTTCGCTTCG | 25929 |
rs4958771 | snp | A/G | 0.299158 | 0.245119 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932751 | TATTTTTTTGTAGAG[A/G]TGAGGTTTCACCATG | 25929 |
rs6580117 | snp | A/G | 0.0807149 | 0.183963 | downstream-variant-500B | GEMIN5 | GRCh38.p7 | 5:154887108 | CTCACTGTCCCAACA[A/G]CTCCAATCCTAGGAA | 25929 |
rs6580118 | snp | A/G | 0.30839 | 0.243086 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905143 | AGTTTGTAGTGAGCC[A/G]AGAGTGTGCCACTGC | 25929 |
rs6580119 | snp | C/T | 0.0503378 | 0.150449 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907555 | TCCCAGACACGACCA[C/T]GAAATCCTAGTGATA | 25929 |
rs6580120 | snp | A/G | 0.288646 | 0.246995 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909533 | TACACCAATTTTTAA[A/G]TACTTTGGTACAAAG | 25929 |
rs6580121 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911659 | ATGTCTTCCTTGCTC[A/G]ATCCTGATCAACTCA | 25929 |
rs6580122 | snp | C/T | 0.498547 | 0.0269177 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924771 | GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 25929 |
rs6860198 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909130 | tgcctgggtaatttt[C/T]gtatttttttttttt | 25929 |
rs6865950 | snp | A/G | 0.17154 | 0.237369 | missense | GEMIN5 | GRCh38.p7 | 5:154896226 | CCCTCTCCACGAAAG[A/G]CCCTTCGGTGCCCGT | 25929 |
rs6879093 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908866 | ctgtttaactactaa[A/G]tatttgcatctacta | 25929 |
rs6879277 | snp | C/T | 0.299411 | 0.245069 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909107 | gggactacaggtgtg[C/T]gacaccatgcctggg | 25929 |
rs7379585 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894141 | ctagagacaggtttt[C/T]gccatgttgcccagg | 25929 |
rs7381141 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907457 | ACTTGAATAAAGCTT[A/G]ACAAAAAAAACTAAT | 25929 |
rs7709899 | snp | A/G | 0.221439 | 0.248363 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901853 | GGCTCAGGCTGGAGC[A/G]CAGTAGCACAATAAT | 25929 |
rs7720521 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904104 | CAAATTTTTTTCTAA[A/G]AAAATGCCATATTAT | 25929 |
rs7720538 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904100 | CCATCAAATTTTTTT[C/T]TAAAAAAATGCCATA | 25929 |
rs7726729 | snp | A/G | 0.245631 | 0.249962 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928234 | ACACTTGAAGTGACT[A/G]AAGCTCAGAAAAGTA | 25929 |
rs7733367 | snp | C/G | 0.093417 | 0.194889 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893903 | agcccgccaccacgc[C/G]cggctaaCACCGATA | 25929 |
rs10037626 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908888 | catctactagttttt[C/G]tattcactgatgttt | 25929 |
rs10042134 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911101 | GAATTCTTTGAGTAC[C/T]GCCTTCCTTTCTGGC | 25929 |
rs10064509 | snp | A/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907459 | TTGAATAAAGCTTAA[A/C]AAAAAAAACTAATGC | 25929 |
rs10075074 | snp | G/T | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888836 | AGCTAACCAAAGTAA[G/T]TGGATTCTAAAttct | 25929 |
rs10477107 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908202 | ttttttttttttgga[A/G]atggtttcgctcttc | 25929 |
rs10515726 | snp | C/T | 0.414576 | 0.188188 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902991 | CTAACCATTATAATA[C/T]CACAGGATGACAGCC | 25929 |
rs10522124 | in-del | -/AGTGAGCCAAGATCCCGCCATTGCACTCCAGCCTGGGCGACAGAGCCAGACTCCGTCTCAAAAAAAAAAAAAAAAGTAATTAATA | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936358 | GGAGGCGGAGCTTGC[lengthTooLong]CTTATTAGTAGTACT | 25929 |
rs10629944 | in-del | -/TC/TTC | 0.0995161 | 0.199636 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901795 | GTGCTTTTTTTTTTT[-/TC/TTC]CCCTTTCCTTTTATT | 25929 |
rs10714011 | in-del | -/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897903 | GGGCTGACTAAGGTG[-/T]TTTTTTTTGTGTTTT | 25929 |
rs11167703 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901163 | AGACTCCGTCTCTAC[A/G]AAAAACTAAAAAATT | 25929 |
rs11167705 | snp | G/T | 0.498568 | 0.0267188 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911191 | CTCCAAGAAGCCATG[G/T]ACATTTTTAGTGGAG | 25929 |
rs11281580 | in-del | -/CCAAACT/TCCAAAC | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900886 | CAAAATGTAGGAGGT[-/CCAAACT/TCCAAAC]AATTCTAGAATATGA | 25929 |
rs11283455 | in-del | -/TCCAAAC | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900885 | TCAAAATGTAGGAGG[-/TCCAAAC]TAATTCTAGAATATG | 25929 |
rs11285608 | in-del | -/A | 0.11963 | 0.213316 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899620 | ATGTGCTTTTTTATT[-/A]AAAAAAAAAAAATGT | 25929 |