SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs495363 | snp | G/T | 0 | 0 | | | | : | TTTTTTTTTTTTTGG[G/T]GGCAGAAATACGGGT | 10075 |
rs812915 | snp | A/G | 0 | 0 | | | | : | TCTAATCCCATCCTA[A/G]ATGAAGTCTGATATG | 10075 |
rs1588144 | snp | A/G | 0 | 0 | | | | : | gttggttggttgtca[A/G]aagctgcttctccta | 10075 |
rs1588146 | snp | A/G | 0 | 0 | | | | : | tcttgaattgcatta[A/G]aatctatagatttgt | 10075 |
rs3761632 | snp | C/T | 0 | 0 | | | | : | TTAATGATTCCTCCC[C/T]ATCTCTTGTGGTGTG | 10075 |
rs3903647 | snp | A/G | 0.0118339 | 0.076006 | | | | : | TTTAAACTATCACCA[A/G]CAATGCAAGAGTCCT | 10075 |
rs4551513 | snp | A/T | 0 | 0 | | | | : | TAACAGTGATCATGG[A/T]ACCCACCATTACCCT | 10075 |
rs11798096 | snp | A/G | 0.00468381 | 0.0481661 | | | | : | TTATATCTCCCTTCA[A/G]GTATCAGTCTCCCTG | 10075 |
rs11798538 | snp | C/T | 0 | 0 | | | | : | GGCTGCTCTAACAAC[C/T]TAGGGCAAAAATCAA | 10075 |
rs11798828 | snp | C/T | 0 | 0 | | | | : | GGAAATGACAGCATG[C/T]TAAGGAGCCCTTCTT | 10075 |
rs12010445 | snp | A/G | 0.00396038 | 0.0443227 | | | | : | CTGCTGTACAGCTTA[A/G]AGAATGAAGCCCCCC | 10075 |
rs12689899 | snp | C/T | 0 | 0 | | | | : | ATATTCCAAATCTTT[C/T]TAAGCCCTTTCACCA | 10075 |
rs12839581 | snp | A/C | | | | | | : | CAAGCATTGTGTTTT[A/C]CAGTTTGGGGTGTTG | 10075 |
rs12841760 | snp | A/G | 0 | 0 | | | | : | CTTAAAGCTGATCTA[A/G]GGACTTCGATGGTTC | 10075 |
rs12846373 | snp | G/T | 0 | 0 | | | | : | TCTTCATGTATATTG[G/T]CTTTGTTTATTGTGT | 10075 |
rs12849688 | snp | G/T | 0 | 0 | | | | : | TTGCTCATTTTCTTG[G/T]TAACTCTTGTTTGAA | 10075 |
rs12861461 | snp | C/T | 0.003992 | 0.0444979 | | | | : | CAGCAAGTGCTCGGC[C/T]TAATCTGGAGGAAGC | 10075 |
rs35905292 | snp | G/T | 0.32 | 0.24 | | | | : | CACTGAGATGTCTCA[G/T]CAAGGCATCTACAAC | 10075 |
rs112855663 | snp | A/C | | | | | | : | AAACCCTTCCTTTTA[A/C]CATGTGTGAGCTGAA | 10075 |
rs200435147 | snp | A/G | | | | | | : | TAGACACTACCCTTT[A/G]TTTTTTTTTTTTTTT | 10075 |
rs201474193 | snp | C/T | | | | | | : | TAATTCCTTTCTTAT[C/T]CCACTTCTATAATTA | 10075 |
rs149215 | snp | G/T | 0.0100156 | 0.0700533 | intron-variant | HUWE1 | GRCh38.p7 | X:53620644 | AATGGTCTCTTAAAT[G/T]GATCTCTCTTTTGCC | 10075 |
rs155441 | snp | A/G | 0.458238 | 0.138337 | intron-variant | HUWE1 | GRCh38.p7 | X:53621903 | CATAAGCATGATGAC[A/G]TTAGCATAGGCTACA | 10075 |
rs198501 | snp | C/T | 0.4741 | 0.110811 | intron-variant, synonymous-codon | HUWE1 | GRCh38.p7 | X:53625883 | tcccggcaccggccc[C/T]ggccccggccccggc | 10075 |
rs198508 | snp | A/G | 0.459151 | 0.136952 | intron-variant | HUWE1 | GRCh38.p7 | X:53640923 | AATATTAGTGTGTTT[A/G]TATCAGCCTAAAAGT | 10075 |
rs266783 | snp | C/G | 0.461978 | 0.132535 | intron-variant | HUWE1 | GRCh38.p7 | X:53594046 | ACCTTGCAGTGAGTT[C/G]AGTTTGCGCCACTGC | 10075 |
rs266784 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | HUWE1 | GRCh38.p7 | X:53593924 | TAACACAGTGAAACC[C/T]CGTCTCTACTAAATA | 10075 |
rs266786 | snp | G/T | 0.495324 | 0.0481281 | intron-variant | HUWE1 | GRCh38.p7 | X:53580794 | CCTTTGATATTAAGT[G/T]TGTGGCCTGGTATAA | 10075 |
rs266787 | snp | A/T | 0.0287145 | 0.11633 | intron-variant | HUWE1 | GRCh38.p7 | X:53580396 | aatacaaattgtgag[A/T]tgttctatataagac | 10075 |
rs369577 | snp | C/T | | | intron-variant | HUWE1 | GRCh38.p7 | X:53593000 | tgttcacagtcatgg[C/T]ggaaggttaagtggg | 10075 |
rs381303 | snp | C/T | 0 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53535639 | AAACAGTGACTTTTT[C/T]TACTACTCATAGCTC | 10075 |
rs391549 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | HUWE1 | GRCh38.p7 | X:53567838 | AGCTCATATTGTATC[A/G]TGGGAGACACATCTC | 10075 |
rs413052 | snp | C/T | 0 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53535712 | AAATACTCTTTGGCT[C/T]TAAGACCTACAAAAA | 10075 |
rs414923 | snp | A/G | 0.448885 | 0.151476 | intron-variant | HUWE1 | GRCh38.p7 | X:53619828 | AGAGAAGAGAGTAAA[A/G]GAAGGCAGAAGGTCA | 10075 |
rs424022 | snp | A/T | 0.0560809 | 0.157783 | intron-variant | HUWE1 | GRCh38.p7 | X:53627567 | TAATCCCTGaaaaaa[A/T]atatatatatatata | 10075 |
rs426298 | snp | A/G | 0.00530186 | 0.0512135 | synonymous-codon | HUWE1 | GRCh38.p7 | X:53536628 | CTCCCGCAGGAGCCC[A/G]CCAGCATCCTGCCCT | 10075 |
rs1039737 | snp | A/G | 0 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53561288 | GTGATGGGGGAGGAA[A/G]AGATTCACTCGTTCT | 10075 |
rs1042970 | snp | A/C | 0 | 0 | utr-variant-3-prime | HUWE1 | GRCh38.p7 | X:53533198 | CAATAAATGAAATCC[A/C]CCAACTCACCGTGTG | 10075 |
rs1055845 | snp | A/T | 0 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53610641 | GTCATAGTATGATGT[A/T]TATGGGGTTTTTTGG | 10075 |
rs1244412 | snp | A/T | 0.462124 | 0.132301 | intron-variant | HUWE1 | GRCh38.p7 | X:53579966 | TTTTTATTTTATTTT[A/T]tttttttaatttttt | 10075 |
rs1244413 | snp | A/T | 0.459 | 0.137183 | intron-variant | HUWE1 | GRCh38.p7 | X:53595118 | ACACTCCATTTTAAG[A/T]AGTATAGGAACAACT | 10075 |
rs1588145 | snp | A/G | 0 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53597121 | cattctccagcttta[A/G]atccttcactttcct | 10075 |
rs1740344 | snp | G/T | 0.0105399 | 0.0718252 | intron-variant | HUWE1 | GRCh38.p7 | X:53598571 | AATATATTTTTCTCT[G/T]AAGATTTTAACATTT | 10075 |
rs1858002 | snp | A/G | 0.473626 | 0.111765 | intron-variant | HUWE1 | GRCh38.p7 | X:53622531 | GGTATTTCCAATTCT[A/G]TAACACAGACTCAAC | 10075 |
rs2036658 | snp | C/G | 0.475654 | 0.107611 | intron-variant | HUWE1 | GRCh38.p7 | X:53655388 | CAATCAGCAGGCATT[C/G]AAGGAAGAGTTTGTG | 10075 |
rs2068538 | snp | G/T | | | intron-variant | HUWE1 | GRCh38.p7 | X:53644666 | CTCAAAGTAACTCAA[G/T]TTTTCAAGCTAATTC | 10075 |
rs2068631 | snp | C/T | 0.0282 | 0.115346 | intron-variant | HUWE1 | GRCh38.p7 | X:53644774 | GGCAACTTCTTAATA[C/T]ATACTTAGCTATGAG | 10075 |
rs2234474 | snp | C/T | 0.0121112 | 0.0768695 | intron-variant | HUWE1 | GRCh38.p7 | X:53537262 | TTTAATATTGCTATA[C/T]TAGGAATGACCATGT | 10075 |
rs2234475 | snp | A/C | 0.0121112 | 0.0768695 | intron-variant | HUWE1 | GRCh38.p7 | X:53536950 | CTCCCCTCCCCACTT[A/C]ACCTAAGCAAGGCCT | 10075 |
rs2234476 | snp | C/G | 0.0256233 | 0.11025 | intron-variant | HUWE1 | GRCh38.p7 | X:53536747 | CCAGACACTGCTTCA[C/G]AGTCTCTCACTCACA | 10075 |
rs2234477 | snp | C/T | 0.0396395 | 0.135087 | intron-variant | HUWE1 | GRCh38.p7 | X:53536301 | ATCCTTGTGCTCCTT[C/T]TTCCCCCCCACTCGC | 10075 |
rs2234478 | snp | A/G | 0.00566568 | 0.052922 | intron-variant | HUWE1 | GRCh38.p7 | X:53534452 | AACGCTAGTTTGTGT[A/G]ATACCAAATAAACCA | 10075 |
rs2267111 | snp | A/G | | | intron-variant | HUWE1 | GRCh38.p7 | X:53565804 | ccggctaattcttgt[A/G]ttttttttatacaga | 10075 |
rs2269599 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | HUWE1 | GRCh38.p7 | X:53534901 | AAAGTGCTAGGATTA[C/T]AAATGTGAGCCACTG | 10075 |
rs2281481 | snp | A/G | 0.0231632 | 0.105096 | synonymous-codon | HUWE1 | GRCh38.p7 | X:53550926 | CAGTAGCACCTCCGC[A/G]CTCTCTGCTATTCTC | 10075 |
rs2295361 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | HUWE1 | GRCh38.p7 | X:53574048 | GCTTAAAGTGGAGGA[G/T]AAATAGCATTCTTTT | 10075 |
rs2333864 | snp | C/G | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | HUWE1 | GRCh38.p7 | X:53686695 | CTAGCGAGGGGAGCA[C/G]GGCTGGAGCAGGGCT | 10075 |
rs3008197 | snp | A/T | 0 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53538724 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 10075 |
rs3008198 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | HUWE1 | GRCh38.p7 | X:53598057 | gaatttcaggatatg[A/G]atctcagtgaaattc | 10075 |
rs3182257 | snp | A/G | | | missense | HUWE1 | GRCh38.p7 | X:53537567 | ATCCCCCGAAGAAAT[A/G]AAGAATCGATTGTAT | 10075 |
rs3736424 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | HUWE1 | GRCh38.p7 | X:53608676 | TGCCAGAAATTAGCC[A/T]ACACAAGCCCCATTA | 10075 |
rs3747437 | snp | C/G | 0.476466 | 0.105893 | intron-variant | HUWE1 | GRCh38.p7 | X:53535692 | GCTTTGGGTAGGAAA[C/G]AGGAAAATACTCTTT | 10075 |
rs3761631 | snp | C/G | 4.55768e-05 | 0.0047735 | synonymous-codon | HUWE1 | GRCh38.p7 | X:53536535 | TGGATTGATGGTGTA[C/G]GTGACTCGATCACCA | 10075 |
rs3761633 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | HUWE1 | GRCh38.p7 | X:53537159 | TCATCTCATCAGCTC[C/G]TACGCTCAGTATTAC | 10075 |
rs3788947 | snp | A/C | 0.477825 | 0.102937 | intron-variant | HUWE1 | GRCh38.p7 | X:53648535 | GCTTAAAAAACAAAA[A/C]AAAACAAAAAAAAAC | 10075 |
rs3788948 | snp | A/C | 0.476695 | 0.105401 | intron-variant | HUWE1 | GRCh38.p7 | X:53648545 | CAAAAAAAAACAAAA[A/C]AAAACAAAAAACAAA | 10075 |
rs3810735 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | HUWE1 | GRCh38.p7 | X:53539604 | GGTCTGCTCTGGGGC[C/T]CTTCCTGCCAGCTTG | 10075 |
rs3834703 | in-del | -/CT | | | intron-variant | HUWE1 | GRCh38.p7 | X:53538720 | cacacacacacacac[-/CT]tctctctctctctct | 10075 |
rs3834704 | in-del | -/TCTC/TCTCTT/TCTT | | | intron-variant | HUWE1 | GRCh38.p7 | X:53538753 | CTCTCTCTCTCTCTC[-/TCTC/TCTCTT/TCTT]ATCAACTAAGGATTA | 10075 |
rs4830378 | snp | G/T | 0.0414859 | 0.13792 | intron-variant | HUWE1 | GRCh38.p7 | X:53592043 | AAAAGTTTTGTAGGT[G/T]ACTAAGGTTTCAGAA | 10075 |
rs5933546 | snp | C/G | 0 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53580773 | CTCATAAATAAATTT[C/G]TGGATTTATACCAGG | 10075 |
rs5933596 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | HUWE1 | GRCh38.p7 | X:53559604 | CTGTTACCATGAGAT[C/T]CTCTTCATGCATCCT | 10075 |
rs5933598 | snp | A/G | 0.01368 | 0.0815649 | intron-variant | HUWE1 | GRCh38.p7 | X:53575377 | CTATAATCTGTGGGA[A/G]GCTATTATAAATACA | 10075 |
rs5933599 | snp | G/T | 0.441341 | 0.160899 | intron-variant | HUWE1 | GRCh38.p7 | X:53620255 | TTGGAGCTTCCATTT[G/T]TCTTTTTTTTTTTTT | 10075 |
rs5933600 | snp | C/T | 0.44509 | 0.156333 | intron-variant | HUWE1 | GRCh38.p7 | X:53620257 | GGAGCTTCCATTTGT[C/T]TTTTTTTTTTTTTTT | 10075 |
rs5978135 | snp | C/G | 0.480631 | 0.0964856 | intron-variant | HUWE1 | GRCh38.p7 | X:53550017 | TCAGCCTCCCAAAGT[C/G]CTGGGATTATAGGTG | 10075 |
rs5978136 | snp | A/G | 0.484947 | 0.0854391 | intron-variant | HUWE1 | GRCh38.p7 | X:53572153 | tcacctgcacacaaa[A/G]tgaatcaagtatgtt | 10075 |
rs5978137 | snp | C/G | 0.337663 | 0.234126 | intron-variant | HUWE1 | GRCh38.p7 | X:53609779 | CAGGAGAGCGGGATG[C/G]GGCAGAGACAGAGGG | 10075 |
rs5978172 | snp | A/G | 0.5 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53566117 | TGTATGTATGTATGT[A/G]TGTGTGTGTGTGTGT | 10075 |
rs5978179 | snp | C/T | 0.110232 | 0.207279 | intron-variant, utr-variant-5-prime | HUWE1 | GRCh38.p7 | X:53649644 | TCTTCTCCTCTAaga[C/T]gtaagttgagggaga | 10075 |
rs5978180 | snp | C/T | 0.324423 | 0.238666 | intron-variant | HUWE1 | GRCh38.p7 | X:53659756 | ctctagtgggagatg[C/T]tgataacaagggagg | 10075 |
rs6529689 | snp | G/T | 0.32505 | 0.238469 | intron-variant | HUWE1 | GRCh38.p7 | X:53639754 | AAAGCAAATACAAAA[G/T]AATGGCATGTAGTTT | 10075 |
rs6638357 | snp | C/T | 0 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53539117 | AAGTAACATTTTACT[C/T]TGCAAACTTCAACAT | 10075 |
rs6638358 | snp | C/T | | | intron-variant | HUWE1 | GRCh38.p7 | X:53539314 | agtgagacctcattt[C/T]tgatttaaaaaaaaa | 10075 |
rs6638359 | snp | C/G | 0.0323082 | 0.122924 | intron-variant | HUWE1 | GRCh38.p7 | X:53577776 | tgatccgccagcctc[C/G]gcctcccgaggcgcc | 10075 |
rs6638360 | snp | C/T | 0.499782 | 0.0104487 | HUWE1 | X | allele_origin=T(germline)/C(germline) | X:53614686 | ATCTGCCTTCTGGAT[C/T]GATGGCTTCTGACAG | 10075 |
rs6638361 | snp | C/T | 0.472271 | 0.114437 | intron-variant | HUWE1 | GRCh38.p7 | X:53640682 | AAGTAGCAAGCCTCT[C/T]AAAGGTAAAAAGTGT | 10075 |
rs6638363 | snp | C/T | 0 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53674854 | GAAtatcaccatctt[C/T]atttaaaggatgagg | 10075 |
rs6638401 | snp | G/T | 0.00237497 | 0.0343779 | intron-variant | HUWE1 | GRCh38.p7 | X:53559566 | TACCATGATCACTGT[G/T]AAGTCCAGAGGTGCC | 10075 |
rs6638408 | snp | C/T | 0.473137 | 0.112738 | intron-variant | HUWE1 | GRCh38.p7 | X:53606532 | gtacatccatgttca[C/T]agcatcattattatt | 10075 |
rs6638409 | snp | C/T | 0.499989 | 0.00236881 | intron-variant | HUWE1 | GRCh38.p7 | X:53632095 | CCTCCTCAAACAATA[C/T]AAAATGACCAGATAA | 10075 |
rs6638410 | snp | C/T | 0.475887 | 0.107121 | intron-variant | HUWE1 | GRCh38.p7 | X:53635874 | CAAAGGTACATACTA[C/T]AGAATGCTATTTCTA | 10075 |
rs6638411 | snp | A/G | 0.475537 | 0.107857 | intron-variant | HUWE1 | GRCh38.p7 | X:53655094 | GACAAGTCCTCCAAA[A/G]CACAAGAAGAAATAA | 10075 |
rs6638413 | snp | A/G | 0.472021 | 0.114921 | intron-variant | HUWE1 | GRCh38.p7 | X:53659580 | CGCAGAGGATTTTTT[A/G]GCCAGTGAAACTACT | 10075 |
rs6638414 | snp | A/G | 0.475537 | 0.107857 | intron-variant | HUWE1 | GRCh38.p7 | X:53663038 | GCTATCACGAGAGAC[A/G]Aaagatggcaagagt | 10075 |
rs6638415 | snp | C/T | | | intron-variant | HUWE1 | GRCh38.p7 | X:53671680 | cacctgtagtcccag[C/T]tactcaaaaggctga | 10075 |
rs6638416 | snp | A/C | 0 | 0 | intron-variant | HUWE1 | GRCh38.p7 | X:53672134 | ACTAGTTTGGAGAAA[A/C]CAGCTTGgaaaaaaa | 10075 |
rs6638417 | snp | A/G | 0.456692 | 0.140635 | intron-variant | HUWE1 | GRCh38.p7 | X:53683019 | CAAACATGAAGACTT[A/G]AGGAAATGGAAGGCT | 10075 |
rs6638419 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | HUWE1 | GRCh38.p7 | X:53686042 | TACAAGACATATTCT[A/C]AGATTTTTAAACAAG | 10075 |
rs6654697 | snp | C/T | 0.0343555 | 0.126481 | intron-variant | HUWE1 | GRCh38.p7 | X:53573179 | ATAAAAAGGGACTTT[C/T]AATAGAACAAATCTC | 10075 |