SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11152 | snp | A/C | 0 | 0 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100211 | AATGTTTATAATATA[A/C]AAAGAAAATACAACC | 25831 |
rs364838 | snp | A/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116120 | TTTATTCTGTTGGCT[A/T]ACAGGAACAGATAAT | 25831 |
rs379586 | snp | C/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119089 | taaggaaacaggagt[C/T]agagtgacgacgagc | 25831 |
rs390725 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118054 | tcacaccactgcact[C/T]cagcctaggtgacag | 25831 |
rs392371 | snp | C/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117799 | AGAGCTCTCTGCCAG[C/T]ATATTTTGTATCTTC | 25831 |
rs397633 | snp | A/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117827 | AGAGTATAAATAGGC[A/G]CAAACTTTTTGTAGA | 25831 |
rs398168 | snp | G/T | 0 | 0 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121193 | ATCCATGATTGCTGT[G/T]ACATAATGCATGCAG | 25831 |
rs399371 | snp | A/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120780 | AAAAGTCATACATGT[A/T]ATAGTAGTTTTGGTT | 25831 |
rs399653 | snp | A/G/T | 0.00472811 | 0.0483911 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120668 | GATGTGCACGTGTGT[A/G/T]CTTACATGCTGTCTG | 25831 |
rs401157 | snp | A/G | 0.497668 | 0.0340657 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122536 | GTGAGCTATAATTGC[A/G]TCACTGCACTCCAGC | 25831 |
rs409451 | snp | A/C | 0 | 0 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116244 | GCGTATTTGGGAGCC[A/C]ACATACACGTAAGAA | 25831 |
rs409667 | snp | A/C | 0 | 0 | missense | HECTD1 | GRCh38.p7 | 14:31116242 | GTATTTGGGAGCCCA[A/C]ATACACGTAAGAAAT | 25831 |
rs417090 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118782 | ctccgcctcctgagt[A/T]gctgagattacaggc | 25831 |
rs424250 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118002 | aaaaaaGACACCTGT[A/T]TTAAATATGAAAGTA | 25831 |
rs430249 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117378 | tttataaaaaaaatt[G/T]ttttttgagatggag | 25831 |
rs433474 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118129 | aatcccagctactca[A/G]gaggctgaggcagga | 25831 |
rs433475 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118126 | cccagctactcagga[A/G]gctgaggcaggagaa | 25831 |
rs433500 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118089 | tgaacccgggaggca[A/G]aggttgcagtgagcc | 25831 |
rs442145 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115052 | TTTTTACAACAGTTA[C/T]agccatgtgctatgt | 25831 |
rs442149 | snp | C/T | 0.4973 | 0.0366419 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115039 | TATAGCCATGTGCTA[C/T]GTAACAACTTTTCAG | 25831 |
rs764790 | snp | A/G | 0.497829 | 0.0328757 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188872 | AGGATGAAGTTGTGT[A/G]TGGAGGGATGGGGGT | 25831 |
rs912673 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183881 | gtctctaccaaaaat[A/C]aaaaaattaactggg | 25831 |
rs1061988 | snp | C/T | 0 | 0 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100263 | GGGGGAAAACCTGGT[C/T]TAAGTGCAAGGCACA | 25831 |
rs1315794 | snp | C/T | 3.40275e-05 | 0.00412463 | missense | HECTD1 | GRCh38.p7 | 14:31113174 | ATGGTGATGAACAGC[C/T]TCAGTTTACTTTTCC | 25831 |
rs1998451 | snp | A/C | 0.490453 | 0.0684267 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208836 | CCTCAATTTCTTGGG[A/C]TCGAGGGATCATCCC | 25831 |
rs2006086 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195222 | ATTGGAGAAAAGCAA[A/G]CTTACATCTTATAAT | 25831 |
rs2031438 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172960 | AATGCTTGTTGAATG[A/G]GTAAAACTTCTATAA | 25831 |
rs2236183 | snp | A/T | 0.498525 | 0.0271165 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104845 | TACAAAACATTTTTT[A/T]AAAAATTAGCTAGAT | 25831 |
rs2273483 | snp | A/G | 0.496263 | 0.0430622 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31113320 | GCTTCTGCGTATTCT[A/G]TATATAGTTGCAAGT | 25831 |
rs2274201 | snp | C/T | 0.498501 | 0.0273349 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178035 | TAGCAGAGACTTAGC[C/T]GAACAGTGTGTAAAG | 25831 |
rs2295530 | snp | G/T | 0.497984 | 0.0316851 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108821 | TGTCACAGGGGTGAA[G/T]CCAACTGGTTTGTTT | 25831 |
rs2295531 | snp | A/C/G | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101841 | ATTTTTTAGTTCTTA[A/C/G]AATTTGTAAGTTCAA | 25831 |
rs2295532 | snp | C/G/T | 0.0185157 | 0.0944193 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101195 | CCTGCATCCCAGGCT[C/G/T]ACGGTTGTACGCAAG | 25831 |
rs3033384 | in-del | -/ATATAT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139042 | ACATATTATATACAG[-/ATATAT]ATATATATATATCTG | 25831 |
rs3033387 | in-del | -/CACACACA/CGCACACA | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163101 | ACACACACGCACACA[-/CACACACA/CGCACACA]TGCGCACACACACAC | 25831 |
rs3742921 | snp | C/T | 0.0528381 | 0.153711 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100179 | ATTTTTTACTTCAAA[C/T]GGCAACAAGTTAAAT | 25831 |
rs3818421 | snp | A/G | 0.49889 | 0.0235361 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132848 | ATTAACATTTTTACT[A/G]TTTTTTAATAATGCA | 25831 |
rs3954287 | snp | C/T | 0.361474 | 0.223771 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102672 | TGACCTCAAGTGATC[C/T]GCCCGCCTTAGCCTC | 25831 |
rs5807613 | in-del | -/CACACACG | 0.0766824 | 0.180169 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163087 | ACACACGCACACACA[-/CACACACG]CACACACGCACACAT | 25831 |
rs6420816 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163493 | ctgtggtcgcaagtg[C/G]ttgggaggctgagtt | 25831 |
rs6571392 | snp | G/T | 0.325091 | 0.238456 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166136 | caggcgtgagccacc[G/T]cacccagccaagata | 25831 |
rs6571393 | snp | C/T | 0.498734 | 0.0251279 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167557 | aagcagaatgattaa[C/T]taaggaggctactgc | 25831 |
rs6571395 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195749 | ctggtctcaaactcg[C/T]gacatcaggtgatcc | 25831 |
rs7140300 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189129 | AACTTGCCCAAAACT[A/G]AAAGACGCTTCTCTA | 25831 |
rs7142646 | snp | C/T | 0.497881 | 0.0324789 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189634 | gggcatggtggtgta[C/T]gcctatagtcccagc | 25831 |
rs7147179 | snp | C/T | 0.341909 | 0.232492 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204175 | gttggttccaagtct[C/T]tgctattgtgaatag | 25831 |
rs7149704 | snp | C/T | 0.497803 | 0.033074 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187085 | tggcgtggtggctca[C/T]gcctgtaatcccagc | 25831 |
rs7150252 | snp | C/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139698 | TGCATCATTTTCCAG[C/T]GATTTGATCAAACAA | 25831 |
rs7150799 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196087 | agtgcaatctgggct[C/T]actgcaacctacacc | 25831 |
rs7154185 | snp | C/T | 0.498964 | 0.02274 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154612 | ctagaatctccttgt[C/T]aatttctacaaaaag | 25831 |
rs7154556 | snp | A/G | 0.337841 | 0.23406 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200417 | ctggaaggccaaggc[A/G]ggaggatcacttaag | 25831 |
rs7157007 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128479 | CTTCATATTCCTGAA[C/G]TGCTAAATTTGATGT | 25831 |
rs7157642 | snp | A/T | 0.152778 | 0.230321 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175874 | tgtctcaaaaaaaaa[A/T]aataataataataat | 25831 |
rs7158847 | snp | G/T | 0.0183471 | 0.0940048 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176313 | agagtgttcttaaga[G/T]acttgcaaaaatgcc | 25831 |
rs7159848 | snp | C/T | 0.347032 | 0.230401 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116083 | AAAACTTAATCATTC[C/T]ACACCAAGAGTCCCA | 25831 |
rs7159930 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193911 | cctgggcaacaagag[C/T]aaaactctgtctcaa | 25831 |
rs7160718 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125693 | AGAAATATAATGACT[C/T]TCTTAAAACTATGGA | 25831 |
rs7494602 | snp | A/T | 0 | 0 | missense | HECTD1 | GRCh38.p7 | 14:31116288 | ATTTCACATTGCCAT[A/T]ACAGGACAATTGAAG | 25831 |
rs8005408 | snp | C/T | 0.0182019 | 0.0936463 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207173 | GGCAAAAGGAGCCGG[C/T]CTGAGGCTCTGGCGC | 25831 |
rs8009645 | snp | A/G | 0.499104 | 0.0211472 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160078 | ATCTATCTCTCTCTc[A/G]tatactgagccatca | 25831 |
rs8010163 | snp | A/T | 0.486876 | 0.0799354 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169058 | CAAAAAAAAAAAAAA[A/T]TTTTTTTTGGTCAAA | 25831 |
rs8015769 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170012 | TCCATCAAACTCTGC[C/T]TCCCAATTTCTTTAA | 25831 |
rs8016033 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154337 | gagtcttgctctgtc[A/G]cccaggctggagtac | 25831 |
rs8018508 | snp | A/G | 0.431473 | 0.171952 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172583 | CCCGCACAACAGAGC[A/G]AGACTCTGTCCCCCT | 25831 |
rs8019897 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158512 | tgatccgcctgcctc[A/T]gcctcccagagtgct | 25831 |
rs8021071 | snp | A/G | 0.497722 | 0.0336691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185337 | GACAAAGAGAGACTC[A/G]GTCTCAAAACAAAAA | 25831 |
rs8021841 | snp | A/T | 0.0901694 | 0.192235 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206628 | TAAAAGttaaaaaaa[A/T]aaaaaaattaaaaaa | 25831 |
rs8022272 | snp | C/T | 0.362732 | 0.22314 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202768 | aacatacattctctc[C/T]tttaatcctcacaag | 25831 |
rs8022903 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188835 | TGAACTCCACCACAC[A/G]TGCCCAATCCCTCAC | 25831 |
rs8023043 | snp | C/T | 0.459233 | 0.136827 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134569 | GTGTGTGTGTGTGTG[C/T]GCGCGTATGTATATA | 25831 |
rs9671411 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199386 | catgtaaggggttta[C/T]tattatAAttttttt | 25831 |
rs9671825 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199059 | aaaaaaaaacagaat[C/T]cacattataactaat | 25831 |
rs9743975 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158540 | gctgggattacaggc[A/G]tgagccaccacgccc | 25831 |
rs9888564 | snp | A/G | 0.413914 | 0.188765 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153535 | Cgtattttgaagagc[A/G]taagtgtgtaatgat | 25831 |
rs10130109 | snp | A/G | 0.497668 | 0.0340657 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152410 | ACCTAGGCTAGGCTC[A/G]AATTCGTGGGCTCAA | 25831 |
rs10130310 | snp | C/T | 0.139903 | 0.224452 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206991 | GCTGTGGTTCCCCAG[C/T]ACCAAACCCCGCTAA | 25831 |
rs10130383 | snp | A/G | 0.49753 | 0.0350569 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176834 | cccacctactcagga[A/G]gctaaggcaggagaa | 25831 |
rs10133173 | snp | A/G | 0.0084209 | 0.0643393 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130355 | TGAACTCTTTTATTA[A/G]AACTATCTGCTAAAG | 25831 |
rs10136065 | snp | C/T | 0.273318 | 0.24891 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154012 | tacactattgtcaca[C/T]tttcttgattaccaa | 25831 |
rs10136398 | snp | C/T | 0.162581 | 0.234218 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145167 | TTAAAAATATATGCT[C/T]AAGTAATGTAAATTT | 25831 |
rs10136918 | snp | C/T | 0.272241 | 0.249009 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118793 | cagctactcaggagg[C/T]ggaggcaggagaatt | 25831 |
rs10136939 | snp | A/G | 0.277778 | 0.248452 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118899 | actccatctcaaggg[A/G]aaaaaaaaaaaaaaa | 25831 |
rs10137852 | snp | A/T | 0.499923 | 0.00618962 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099865 | GATCTGGTGTTTTTT[A/T]AAAAAAATAACACAA | 25831 |
rs10137998 | snp | C/T | 0.496999 | 0.0386216 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136830 | ATTCTTTTTTTTTTT[C/T]TTTTTTTCTGAGACG | 25831 |
rs10142413 | snp | A/G | 0.244205 | 0.249933 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191725 | CAGAGAAGGGCTggc[A/G]tggtggctcacgcat | 25831 |
rs10145294 | snp | C/T | 0.498589 | 0.02652 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153314 | ggagaatggcttgaa[C/T]ccgggaggcagagct | 25831 |
rs10146042 | snp | C/T | 0.283947 | 0.247685 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140919 | AATGGCCAATCTCCA[C/T]CCAGGtttttttctt | 25831 |
rs10146272 | snp | A/G | 0.364401 | 0.222289 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187684 | gaactgaaaatacag[A/G]aagagaaaactagca | 25831 |
rs10147747 | snp | C/T | 0.243633 | 0.249919 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169905 | aCAATACAAAGCAGC[C/T]TATCGTAACTTGAAA | 25831 |
rs11156658 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152737 | TAATTAAACAATAAA[A/T]AAATAAAGAGGCCAG | 25831 |
rs11323906 | in-del | -/A | 0.213635 | 0.247341 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200490 | GTCTCCATCTAATTT[-/A]AAAAAAAAAAAAAAA | 25831 |
rs11342454 | in-del | -/T | 0.49889 | 0.0235361 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154811 | GGGATTCTACAATTA[-/T]TAACTCATATACCAC | 25831 |
rs11420686 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208930 | CCAAAATACTGGTTC[-/T]TTTTTTTTCTTTCTT | 25831 |
rs11450805 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188237 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 25831 |
rs11549801 | snp | C/T | | | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101047 | TGCTACTGATGCAAG[C/T]TATCCATCAGTCAAT | 25831 |
rs11620816 | snp | C/T | 0.299422 | 0.245066 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150186 | ATATGGTTTACCTTG[C/T]TGCAATTCTTTAGCA | 25831 |
rs11620871 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182445 | caatctgtccacctc[A/G]gcctcccaaagtgct | 25831 |
rs11622403 | snp | C/G | 0.248911 | 0.256152 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208115 | AAAGCTGCGGCCCAA[C/G]CTGTCCCCGCTGAGC | 25831 |
rs11625570 | snp | A/G | 0.225301 | 0.248777 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168609 | TAGAACATTGTTTCA[A/G]TGATGCTTATAAGAA | 25831 |
rs11625694 | snp | C/T | 0.258565 | 0.249853 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161565 | GACACAGCAACACCC[C/T]GTCTCAAAAAAAAAG | 25831 |
rs11625798 | snp | A/G | 0.344147 | 0.231595 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161712 | cacccgagatgagga[A/G]ttcgagaccagccca | 25831 |
rs11626343 | snp | A/G | 0.237593 | 0.249692 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204460 | ACTTTTTTAAATGTC[A/G]TAACAAATACTTCTA | 25831 |
rs11626909 | snp | A/G | 0.029116 | 0.117091 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132599 | GCAAATTATCTGCTA[A/G]TAAGTCAGCCTTATA | 25831 |
rs11844935 | snp | A/G | 0.498754 | 0.0249289 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195061 | AAGACAATAAATAAC[A/G]CAACATCTTTTGATC | 25831 |
rs11845340 | snp | A/C | 0.00379505 | 0.043395 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123125 | GCATTTTAGGTTTTT[A/C]CAAAACAAAAGTAAA | 25831 |
rs11845860 | snp | A/C | 0.303043 | 0.244308 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148674 | ACCACTGAAAATTTA[A/C]CAAATCAGTATAAAA | 25831 |
rs11847959 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146718 | atgagccgggcatgg[G/T]ggcgcgcacctgtaa | 25831 |
rs11848094 | snp | A/G | 0.318415 | 0.240457 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112765 | TAGGCATGTGCCACC[A/G]TGCCCAGCTAATTTT | 25831 |
rs11848563 | snp | C/T | 0.376195 | 0.215812 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152168 | TGATACTGCATAAGA[C/T]TGGGCAAAGAACAAC | 25831 |
rs11848635 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138745 | TTCTCAGAGGTATGG[C/G]AAGTTTTGTTAGCTT | 25831 |
rs11850455 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196235 | ttggccaggttggac[G/T]tgtactccggaattt | 25831 |
rs11850716 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169999 | ACATGTCACCTTCTC[C/T]ATCAAACTCTGCCTC | 25831 |
rs11850963 | snp | C/T | 0.242775 | 0.249896 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170704 | CAGGCTAGAAAGCTA[C/T]GAACCTGTTATTGAA | 25831 |
rs11851654 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115991 | TCATACACGATCTTA[A/G]ACAAAGAATTCAAAT | 25831 |
rs12100457 | snp | C/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189247 | TCTAAAATACAAAAT[C/G]TAAGACTTAATCTTG | 25831 |
rs12100469 | snp | A/G | 0.127254 | 0.217792 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189460 | ATCCTTCAGTACCCT[A/G]AGGATAAAATCCAAA | 25831 |
rs12100629 | snp | G/T | 0.0883596 | 0.190715 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162305 | CCTAATATTTTAGTT[G/T]TTAAGTCTTAGAATT | 25831 |
rs12433463 | snp | A/C | 0.00835141 | 0.0640778 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209030 | CGCATGTCCCGTTGT[A/C]GCAGGTAATGGTCCG | 25831 |
rs12433524 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202035 | ctcacgcctgtaatt[C/G]cggcactttgggagg | 25831 |
rs12436102 | snp | A/G | 0.11228 | 0.208646 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205383 | CATATGACAACATCA[A/G]TGAAGAAATGGGCAG | 25831 |
rs12436156 | snp | A/C | 0.162581 | 0.234218 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145443 | caaggcaggcagatc[A/C]cttgaggtcagtcag | 25831 |
rs12586288 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159714 | gcaggattttgactc[A/T]ctgcaacctccgact | 25831 |
rs12588474 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119923 | AAATTTCATTGTTGC[A/C]AAAGCAATGTGTTAT | 25831 |
rs12590867 | snp | A/G | 0.030278 | 0.119257 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194233 | caccaagtgccaggc[A/G]ttgggatggggaaag | 25831 |
rs12879008 | snp | A/G | 0.046775 | 0.145601 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143593 | AGCAGAATGTGACTC[A/G]AGCGCTACATTTCCA | 25831 |
rs12879653 | snp | A/G | 0.177182 | 0.23916 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110582 | GAAAACAAACAGTTT[A/G]AATTATAACTTTTTT | 25831 |
rs12880208 | snp | C/T | 0.2462 | 0.249971 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182294 | cttctaggctcaacc[C/T]tcctcccacctcagc | 25831 |
rs12880903 | snp | A/C | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177535 | aataataataataat[A/C]ctattcctggcacca | 25831 |
rs12882134 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156308 | cggtggtgcgatctc[A/G]gctcactgcaacctc | 25831 |
rs12884045 | snp | C/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190246 | agagacaagccatct[C/T]cactctaccctttcc | 25831 |
rs12885080 | snp | C/T | 0.046775 | 0.145601 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160752 | ctcagctcactgcag[C/T]ctcgaccgcccaggc | 25831 |
rs12885225 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190156 | gaacaaatcatctgg[G/T]gattctagtgcctaa | 25831 |
rs12885256 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190213 | atttcctagctgagg[G/T]cccagatatcgcaga | 25831 |
rs12888536 | snp | C/G | 0.134119 | 0.221521 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108359 | cctcccaaagtgctg[C/G]gattacaggcatgag | 25831 |
rs12888959 | snp | C/T | 0.283421 | 0.247756 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141733 | ATTATACATGTATAA[C/T]ATGTTACTTTCTTAT | 25831 |
rs12894223 | snp | C/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188243 | ttattcttccttttt[C/T]ttttttttttgagac | 25831 |
rs12897384 | snp | G/T | 0 | 0 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31210018 | TTTACCAAGtttttt[G/T]ttgtttttttttttt | 25831 |
rs12897385 | snp | G/T | 0.277778 | 0.248452 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31210021 | ACCAAGttttttgtt[G/T]ttttttttttttttt | 25831 |
rs17097730 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104619 | CCCATCATGATTCTT[C/T]CATGTTAATTCATCC | 25831 |
rs17097735 | snp | C/T | 0.297818 | 0.245384 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31109556 | TGTGGTTCTCGTTCG[C/T]TCCACAGTGGCTTCA | 25831 |
rs17097740 | snp | C/T | 0.0562307 | 0.157967 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121151 | TATTACCCAAAGCAA[C/T]GTAAAGGGGTTTCAA | 25831 |
rs17097741 | snp | A/G | 0.414245 | 0.188477 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126460 | TTGCAAGAATCATGC[A/G]TTACCTAACTAAGGA | 25831 |
rs17097743 | snp | A/G | 0.231256 | 0.249296 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129042 | GGTGCTTGCACTGGA[A/G]GATGACCCTACTTCT | 25831 |
rs28377925 | snp | C/T | 0.326506 | 0.238006 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102676 | CTCAAGTGATCCGCC[C/T]GCCTTAGCCTCCCAA | 25831 |
rs28393728 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158718 | GGAGGCTGAGGCAGG[C/T]GGATCACCTGAGGTC | 25831 |
rs28417029 | snp | A/G | 0.121022 | 0.21416 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172453 | ACACAAAAATTAGGC[A/G]GGTGTGGTGGCACAT | 25831 |
rs28495544 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190019 | GGACTCATGCTCTTA[A/G]AACCCAGTCACCATC | 25831 |
rs28591281 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143429 | AAAAATAAATAAATA[C/T]ATAAACAAAGGAAAA | 25831 |
rs28806860 | snp | A/G | 0.278399 | 0.248382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125022 | CATATTGGCCAGGCT[A/G]GTCTCGAACTCCTGA | 25831 |
rs33983486 | snp | C/T | 0.174451 | 0.238311 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178233 | TTTGCAAAGGGCTGG[C/T]AAGAAAGTGCGAGGA | 25831 |
rs34013333 | in-del | -/A | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155345 | GCAAGATACCGTCTC[-/A]AAAAAAAAAAAAAAG | 25831 |
rs34042150 | in-del | -/C | 0.257732 | 0.24988 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188242 | TTATTCTTCCTTTTT[-/C]TTTTTTTTTTTGAGA | 25831 |
rs34105672 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105587 | TAAAAGCAAACTTTT[-/T]ACCTCATCTTCACCA | 25831 |
rs34140783 | in-del | -/A | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192336 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 25831 |
rs34211256 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31119002 | GCTTCATTCTTTCTA[A/G]AGGCTCTAGAGAAGA | 25831 |
rs34211468 | in-del | -/GTGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134566 | TGTGTGTGTGTGTGT[-/GTGC]GCGCGTATGTATATA | 25831 |
rs34261656 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159629 | AGGCGTGAGCCACCG[-/G]CACCTGGCCATAATT | 25831 |
rs34267515 | in-del | -/A/AA | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191545 | AAAAAAAAAAAAAAA[-/A/AA]TTACTAACTGATTGA | 25831 |
rs34305380 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31140270 | TTACTGGATAATATT[-/C]TGATAAATAAAAAAG | 25831 |
rs34324709 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205886 | TCCCTTTCATCTCCC[-/C]TGTCCCATCTGTAGC | 25831 |
rs34326211 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154835 | ATACCACCATTTTTT[-/T]CAAAAATATTACTAC | 25831 |
rs34329903 | in-del | -/GT/TG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122380 | TGTGTGTGTGTGTGT[-/GT/TG]CATTCTGTGGCTCAG | 25831 |
rs34350304 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122510 | GTGTTTGTGTCATTC[-/C]TGTGGCTCAGGCTGG | 25831 |
rs34434300 | in-del | -/A | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163260 | AGACTTCATCTCTAC[-/A]AAAAAAAAAAAACTA | 25831 |
rs34447978 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163078 | CACACACACACACAC[-/AC]GCACACACACACACA | 25831 |
rs34468018 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205013 | ATAAAGAAACATCAG[-/G]AGTTTTCAATTACTT | 25831 |
rs34468329 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186709 | AAAAAAAAAAAAAAA[-/A]TCCCACCAATTAAGC | 25831 |
rs34511250 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149040 | TCAAACATGTCAGTG[-/C]ACCAATTTCCTACAG | 25831 |
rs34513326 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138355 | CTGTATAAATCTTAA[-/C]TAATTCCTATAAAAA | 25831 |
rs34588788 | snp | A/C | 0.151596 | 0.229819 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133460 | CAAATCACTTTTTAC[A/C]AAAGTAATTGTTTTA | 25831 |
rs34636684 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122963 | CATCTTCATTCTCAT[-/G]CATCTTCTTCATCTG | 25831 |
rs34666986 | snp | C/T | 0.184618 | 0.241299 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178242 | CAGATGTCCTCCTCG[C/T]ACTTTCTTACCAGCC | 25831 |
rs34684806 | snp | C/T | 0.361474 | 0.223771 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156135 | GTCTGCAGTCCCAGC[C/T]ACTGGGGAGGCTGAG | 25831 |
rs34745649 | snp | A/G | 0.237014 | 0.249662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204729 | ACTCAAAATTCTGCC[A/G]ATGACAAAAACTAAT | 25831 |
rs34755108 | in-del | -/T | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157279 | AAAATGAATCATTTT[-/T]CGAATTAGAGCAAGA | 25831 |
rs34767404 | in-del | -/AG | 0.497668 | 0.0340657 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108115 | TTTATTTTTTGAGAC[-/AG]AGTTTCACTCTTGTC | 25831 |
rs34807591 | snp | C/T | 0.247053 | 0.249983 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196570 | CCAGCCTGGCCTATA[C/T]GGTGAAACCCTGTCT | 25831 |
rs34887127 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134468 | ATGGAGAGTTTATGG[-/G]AAAGTTTATTTCACT | 25831 |
rs34975239 | snp | C/T | 0.277067 | 0.24853 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146069 | ATGAAATTTCAGTAT[C/T]CTGTAGTCTAGATTT | 25831 |
rs35018572 | in-del | -/A | 0.216649 | 0.247765 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163913 | GCAAGACTCTGTCTC[-/A]AAAAAAAAATTTTTT | 25831 |
rs35038159 | in-del | -/T/TG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125191 | TTTTTTTTTTTTTTT[-/T/TG]GAGACAGAGTCTTGC | 25831 |
rs35112928 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195617 | CCTCCGCCTCCCAGG[-/G]TCAAGCAATTCTCCT | 25831 |
rs35119057 | in-del | -/A | 0.243347 | 0.249911 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180022 | CTCTACTAAAAATAC[-/A]AAATAATTAGCCGGG | 25831 |
rs35121220 | in-del | -/C | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208667 | GTTTCCTGTAATCCC[-/C]AGCACTTTATGATTT | 25831 |
rs35121269 | snp | C/T | 0.490997 | 0.0664859 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208688 | TTTATGATTTTACTC[C/T]CTTGAGGCCCGGAGT | 25831 |
rs35139866 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165304 | CACCATCTAACTGGT[-/G]CACCAATCCCTATAC | 25831 |
rs35158504 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155235 | TGTAATCCCAGCTAC[-/C]GCCGGAGGCTGAGGC | 25831 |
rs35160077 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158990 | GTCTATTATGTAAGA[G/T]CCAATAATCAATTCA | 25831 |
rs35178403 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115637 | CGTGGTGCACACCTG[-/G]TAGTCCCAGCTACTC | 25831 |
rs35199827 | in-del | -/A | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191859 | CAAAAAAAAAAAAAA[-/A]TTAGCCAGATGTGGT | 25831 |
rs35249296 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183079 | CACAAAAAAGGTAAA[-/A]AAAAAATCCCAGATT | 25831 |
rs35311292 | snp | C/G | 0.00337301 | 0.0409283 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168320 | GCACAAACATTTCAG[C/G]AAACTATGCTGCCTT | 25831 |
rs35330573 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200676 | TTCCAGTTACTGGGG[-/G]CGGCTGAGGCAGGAG | 25831 |
rs35334871 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149703 | GGTCAGGAGTTCGAG[-/T]ACTAGCCTGACCAAC | 25831 |
rs35376710 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105873 | AAGTTGAGGACTTTT[-/T]AAATGCAATATTCTA | 25831 |
rs35407911 | snp | C/T | 0.00977458 | 0.0692225 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149087 | TACTTCAAGTCAACC[C/T]ATACTGTCAGCACCA | 25831 |
rs35501234 | in-del | -/C | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206955 | CGGCCGAGCCGGGCG[-/C]TGAGAGGCGCTGGCC | 25831 |
rs35553721 | in-del | -/A | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156804 | AAAAAAAAAAAAAAA[-/A]CTCTTCCTGATACCT | 25831 |
rs35654594 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103940 | CCATCACACTCCAGC[-/C]TGGGAAACAAGAGCA | 25831 |
rs35654935 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152758 | AGAGGCCAGGTGCGG[-/G]TGGATCACTTTGAGG | 25831 |
rs35657739 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187246 | GTAGTCCCAGCTCCC[-/C]TGCTGGGAGGCTGAG | 25831 |
rs35688568 | in-del | -/A | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200511 | AAAAAAAAAAAAAAA[-/A]GGTCACACCTGTAAT | 25831 |
rs35760972 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200332 | CTTACTCATCCTTCC[-/C]TAGCTCTAGGAAAAA | 25831 |
rs35822451 | in-del | -/ATG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159077 | ATTACCCTTGAGGTG[-/ATG]AATGATAGAAGGATA | 25831 |
rs35824069 | in-del | -/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122639 | AAGTGTGGGACTACA[-/G]GGCATGAGCCCTATA | 25831 |
rs35852948 | snp | A/C | 0.196149 | 0.244131 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193249 | GGTTTTTAAAAATAT[A/C]TATAGTGTGAGATAG | 25831 |
rs35879052 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126774 | GGGGCCTTGAACTTC[-/C]AGGGCTCAAGTAACC | 25831 |
rs35920813 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130805 | CCCAAATCTACATAA[-/A]GTAGCTTAGATGAGA | 25831 |
rs35943542 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197769 | AAAGTTTCCACATGT[-/G]CCTCCATTTCATGTT | 25831 |
rs35996017 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176836 | CACCTACTCAGGAGG[-/C]TAAGGCAGGAGAACC | 25831 |
rs35999346 | in-del | -/T | 0.26078 | 0.249767 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140933 | ATCCAGGTTTTTTTC[-/T]TTTTTTTTTTTTGTT | 25831 |
rs36087394 | in-del | -/T | 0 | 0 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31210033 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGT | 25831 |
rs36092473 | in-del | -/AAT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138357 | GTATAAATCTTAACT[-/AAT]TCCTATAAAAACAAT | 25831 |
rs36093483 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115588 | CATGGTAAAAACCCC[-/C]ATCCCTACAAAAAAT | 25831 |
rs36100814 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193047 | TGGATAATCCTATAT[-/A]CTATCACATAAACTA | 25831 |
rs36110747 | snp | C/T | 0.000896831 | 0.0211568 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149083 | TCAAGTCAACCTATA[C/T]TGTCAGCACCAGGAC | 25831 |
rs45450991 | snp | A/G | 0.00967451 | 0.0688742 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150084 | TCTGAACCATCCATT[A/G]CTGCCATTAGATAAT | 25831 |
rs45494101 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129541 | ATCAGCTTTTCATCA[C/G]TGCTGTCCTTTTCTG | 25831 |
rs45610935 | snp | C/G | 0.282369 | 0.247896 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112836 | GCTGGTCTCGAACTC[C/G]TAGCCTCTAACGATA | 25831 |
rs45627031 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31173488 | CAAAAACACTTTTTC[C/T]GAAGATTAAAAAGCA | 25831 |
rs55641498 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190807 | AGTCGCTGCGCCAGG[A/C]CCTATTTTTTATACA | 25831 |
rs55718189 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122550 | ATGCAATTATAGCTC[A/G]CTGCAGCCTGCAACT | 25831 |
rs55738904 | in-del | -/T | 0.436123 | 0.166908 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177890 | TGAAGATAGGAAGAA[-/T]TTTTTTTTTTAGAAA | 25831 |
rs55803868 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110601 | TATAACTTTTTTTTT[A/T]CAACTATTTTGGAAG | 25831 |
rs55919315 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144117 | TAAACTTACATTGTT[-/T]AACACAGTAAGAAGT | 25831 |
rs56112971 | snp | A/G | 0.040671 | 0.13668 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164602 | CTTGGAGACGAGCCA[A/G]TTGATTAAGAGGTTA | 25831 |
rs56168081 | snp | C/T | 0.372995 | 0.217652 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122148 | CATACACTGTGTGTG[C/T]GCTTGGGTGTGTGTG | 25831 |
rs56256167 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145138 | GTCTGATGAAATTTA[A/G]TACATGATATTATTT | 25831 |
rs56281723 | snp | C/T | 0.431769 | 0.17164 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152427 | ATTCGTGGGCTCAAG[C/T]GACCTGTCCGCCTCG | 25831 |
rs56297437 | snp | C/T | 0.00737262 | 0.0602657 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119673 | ATCTGATTTAGTATG[C/T]ATTAAAATTAAATCA | 25831 |
rs56301232 | snp | A/G | 0.081446 | 0.184634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205256 | TCCCCAAACTTCAAA[A/G]TGTTTCTACTACTCC | 25831 |
rs56346233 | snp | A/T | 0.414905 | 0.187899 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122197 | TGGCTCAGGCTGGAA[A/T]GCAGTGATGCAATTA | 25831 |
rs56659016 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124057 | AGTAACAGAAAAAAA[-/A]TGGTGTGTCTTAACA | 25831 |
rs56705267 | in-del | -/ACTA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133197 | AAAAGAAAAAATTTA[-/ACTA]CCCATTTTCTACACA | 25831 |
rs56708555 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127438 | CTCACTGTAACCTCC[A/G]CCTCCTGGGCTCAAG | 25831 |
rs56919671 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127515 | TGCCACCACTCCCGG[A/C]TAATTTTCTTTTGTA | 25831 |
rs57000706 | snp | C/T | 0.376394 | 0.215696 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153500 | AGGCATGAGGCATCA[C/T]GCCCAGCCGACCATT | 25831 |
rs57054894 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200846 | CCACCTCTCCAGGTC[-/C]TTGTCCCTGCTTCAT | 25831 |
rs57055616 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127448 | CCTCCGCCTCCTGGG[C/T]TCAAGCAATTCTTCT | 25831 |
rs57111746 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167271 | GAGTTTGAGACCAGC[A/C]TGGGCAACGTGGTGC | 25831 |
rs57203195 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191705 | CCAGCTTTCACTTAA[A/G]AAAACAGAGAAGGGC | 25831 |
rs57218917 | in-del | -/TAAAATAAAATAAAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179455 | TAAAATAAAATAAAA[-/TAAAATAAAATAAAA]CAAAATAAAATAAAT | 25831 |
rs57282450 | in-del | -/AGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127469 | CAATTCTTCTGCCTC[-/AGC]CTCCTGAGTAGCTGG | 25831 |
rs57367858 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127576 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 25831 |
rs57398117 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140342 | GGGTATCACAACATA[C/T]ACTTTCTCATTATTA | 25831 |
rs57460229 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106104 | ACAAAAATATATATT[A/T]AAAAAAACCTTGAAT | 25831 |
rs57571091 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127509 | GGCGTGTGCCACCAC[G/T]CCCGGATAATTTTCT | 25831 |
rs57574678 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127461 | GGCTCAAGCAATTCT[C/T]CTGCCTCAGCCTCCT | 25831 |
rs57583935 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188965 | ACAAACAACTGAATC[C/G]ACTTCCATCTCTCAT | 25831 |
rs57637297 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135742 | ATGCTCATTTAGGCC[A/G]GGTGCGGTGGTTCAC | 25831 |
rs57637783 | snp | G/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148906 | ACTTACCCAGGGAAG[G/T]TTCTGCAGTAAATGA | 25831 |
rs57677211 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163102 | ACACACACGCACACA[C/T]GCGCACACACACACA | 25831 |
rs57702700 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127455 | CTCCTGGGCTCAAGC[A/G]ATTCTTCTGCCTCAG | 25831 |
rs57869643 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122304 | ATTCTGTGGCTCAGG[C/T]TGGAGTGCAGTGACA | 25831 |
rs57893693 | snp | A/G | 0.235854 | 0.249599 | intron-variant | HECTD1 | GRCh38.p7 | 14:31164830 | CAATAAGGGAACTCT[A/G]TTACATGGTAGCATA | 25831 |
rs57944890 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196773 | CAAAAAAAAAAAAAA[A/G]AAAGAAAAGGCAGGT | 25831 |
rs58071351 | snp | G/T | 0.41408 | 0.188621 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125242 | GCAAATGGCACAATC[G/T]TGGCTCAATGCAACC | 25831 |
rs58127013 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111092 | CCATCTCACATCTTT[-/T]CAGCAAGAAATACAT | 25831 |
rs58204331 | snp | C/T | 0.41325 | 0.18934 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130072 | GTAAAAGTTTTAAAA[C/T]TGCTAAATATAATTA | 25831 |
rs58325016 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199052 | AAAAAAAAAAAAAAA[-/A]CAGAATCCACATTAT | 25831 |
rs58334157 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127405 | TGCCCAGGCTGGAGT[A/G]CAATGGCGCGATCTC | 25831 |
rs58498783 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127365 | TGTTTTCTGTTTTTT[C/T]TTTGAGAAGGAGTTT | 25831 |
rs58527406 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181536 | AGGAAGCTCATGTGA[A/T]TCCAGGAAATCAAGG | 25831 |
rs58528668 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127412 | GCTGGAGTGCAATGG[C/T]GCGATCTCTGCTCAC | 25831 |
rs58587344 | in-del | -/TG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122286 | GTGTGTGTGTGTGTG[-/TG]AGATTCTGTGGCTCA | 25831 |
rs58646413 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191831 | TGGAGAAAACCCCGT[C/T]TCTGCTAAAAATACA | 25831 |
rs59058028 | snp | A/C/T | 0.0229158 | 0.10471 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159628 | ACAGGCGTGAGCCAC[A/C/T]GCACCTGGCCATAAT | 25831 |
rs59300309 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127480 | CCTCAGCCTCCTGAG[G/T]AGCTGGGATTACAGG | 25831 |
rs59458716 | snp | C/T | 0.234692 | 0.249531 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172965 | GAAGTTTTACCCATT[C/T]AACAAGCATTTATTC | 25831 |
rs59605884 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176958 | AAAAAAAAAAAAAAA[-/A]TCATGTAAAATCTCA | 25831 |
rs59655365 | snp | A/C | 0.430434 | 0.173042 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139289 | TGTTAAAACTTAATC[A/C]CCAGTGCAGTGGTGT | 25831 |
rs59860266 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130361 | CTTTTATTAGAACTA[C/T]CTGCTAAAGCTAATA | 25831 |
rs59933112 | snp | C/T | 0.237303 | 0.249677 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204788 | AATTTGGAAATTTTA[C/T]TAGTAAGGATTTTTA | 25831 |
rs59998659 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122262 | AGTTCATACACACAC[A/G]CGTGTGTGTGTGTGT | 25831 |
rs60131207 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134757 | AGTGATTTGTTTTTA[A/G]AAAGAAAATTTTGCT | 25831 |
rs60159373 | in-del | -/GCC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127464 | TCAAGCAATTCTTCT[-/GCC]TCAGCCTCCTGAGTA | 25831 |
rs60190549 | in-del | -/AAAAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118922 | AAAAAAAAAAAAAAA[-/AAAAA]CTACCACAAATTTAT | 25831 |
rs60350855 | snp | G/T | 0.21875 | 0.248039 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192323 | CCTGGGTGACAGAGC[G/T]AGACTCTGTCTCAAA | 25831 |
rs60383366 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127489 | CCTGAGTAGCTGGGA[C/T]TACAGGCGTGTGCCA | 25831 |
rs60451564 | in-del | -/TAGA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188142 | AGATAGATAGATAGA[-/TAGA]CAGACAGATAAAAGC | 25831 |
rs60504452 | in-del | -/GT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122399 | TGTGTGTGTGTGTGT[-/GT]CATTCTGTGGCTCAG | 25831 |
rs60599674 | snp | C/T | 0.0886483 | 0.19096 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122263 | GTTCATACACACACA[C/T]GTGTGTGTGTGTGTG | 25831 |
rs60642562 | in-del | -/TG | 0.490398 | 0.0686206 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198205 | TCTACTTAAAGGAAA[-/TG]GGAATTAATTATAAA | 25831 |
rs60754005 | in-del | -/CC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185846 | AATGAACGACCCCCC[-/CC]ACATTCCCTAGGTCT | 25831 |
rs60774875 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137284 | TACAGGTGCGTGCCA[C/T]CACGCCCGGCTACTT | 25831 |
rs60867794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167675 | GAGAGCCACAAGGAG[C/T]TCCTGATGGATGGAT | 25831 |
rs60928004 | snp | A/T | 0.407674 | 0.194008 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119123 | ACATGTTCTTCTCTG[A/T]CTCCTGCCTCTTGTG | 25831 |
rs60956918 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127497 | GCTGGGATTACAGGC[A/G]TGTGCCACCACTCCC | 25831 |
rs61004717 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127358 | TGTTTGTTGTTTTCT[G/T]TTTTTTTTTTGAGAA | 25831 |
rs61129287 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137536 | TAGGAGTTCAAGACC[C/G]GCCTGGGCAACACAG | 25831 |
rs61181287 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127532 | AATTTTCTTTTGTAT[G/T]TTTAGTAGAAATGGG | 25831 |
rs61197871 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134555 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTG]CGCGCGTATGTATAT | 25831 |
rs61224896 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127542 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTTACCAT | 25831 |
rs61238303 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127552 | GTAGAAATGGGGTTT[C/T]ACCATGTTGGTCAGG | 25831 |
rs61240248 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127442 | CTGTAACCTCCGCCT[C/T]CTGGGCTCAAGCAAT | 25831 |
rs61300170 | snp | A/C/G | 0.0792508 | 0.182605 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199017 | CTCCAACCTGGGTGC[A/C/G]AGAATCTGCCTCGAA | 25831 |
rs61321077 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202235 | GTGGAGAGCCATGTA[C/T]AATACTAAGTTAAAG | 25831 |
rs61422236 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127500 | GGGATTACAGGCGTG[C/T]GCCACCACTCCCGGA | 25831 |
rs61519970 | in-del | -/AA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165014 | TAAAAAAAAAAAAAA[-/AA]GTGACCCCACTAACA | 25831 |
rs61592116 | snp | A/C | 0.258565 | 0.249853 | intron-variant | HECTD1 | GRCh38.p7 | 14:31164883 | TATCATGAAGCACTT[A/C]TACTCCAGAATGATT | 25831 |
rs61616415 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200333 | CTTACTCATCCTTCC[C/T]AGCTCTAGGAAAAAC | 25831 |
rs61639709 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127454 | CCTCCTGGGCTCAAG[C/T]AATTCTTCTGCCTCA | 25831 |
rs61671400 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127373 | GTTTTTTTTTTGAGA[A/T]GGAGTTTCGCTCTTG | 25831 |
rs61976858 | snp | A/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108660 | GAGAACTTGTCTCTA[A/T]TAAAAAAAAAAAAAA | 25831 |
rs61976859 | snp | C/T | 0.187573 | 0.24208 | missense | HECTD1 | GRCh38.p7 | 14:31114306 | TTCCATTTTCCTTTT[C/T]TTTATCAGAATCCTT | 25831 |
rs61978760 | snp | A/G | 0.274661 | 0.248781 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120039 | CATTTCAGTTTACCC[A/G]AAGTAAGTTGCATCA | 25831 |
rs61978761 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131261 | GATTTTTTTTTTTCC[C/T]ATCTGTGGCAGCTAA | 25831 |
rs61978762 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131554 | ATAGGAATGTCACAG[C/T]GCAAGATGCTGCTAG | 25831 |
rs61978763 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131643 | GTGCCATTGTATCTT[A/G]GGAAAAAAAAAAAGA | 25831 |
rs61978764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143271 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGCAGGT | 25831 |
rs61978766 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148516 | TCCATTTTGATTCTG[C/T]TTTAATGTTGGTATT | 25831 |
rs61978767 | snp | A/G | 0.129664 | 0.219133 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152690 | AACATTGTGAGACCC[A/G]CATCTCTACAAAAAT | 25831 |
rs61978768 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162797 | TTTTAAAAAAAAAAT[A/T]GGGCCAGTCGCAGTG | 25831 |
rs61978769 | snp | C/T | 0.0912534 | 0.193131 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163823 | GAGGCTGAGGCAGGA[C/T]AATCACTTGAACCCA | 25831 |
rs61978770 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176138 | AAGAACTACAAGTAA[C/T]TTAGCAAAAGCTCAT | 25831 |
rs61978772 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178827 | AAAAAAAAAAAAAAT[A/T]CAGCGCTCACCTCAA | 25831 |
rs61978773 | snp | A/C | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181638 | AAAAAAAAAAAACAA[A/C]AACAAAAAAACAGAG | 25831 |
rs61995486 | snp | C/T | 0.127944 | 0.218179 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199853 | GAAGTCCTGAGACCA[C/T]AGAGTTTAAGCATCA | 25831 |
rs61995487 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200487 | CTTGTCTCCATCTAA[A/T]TTAAAAAAAAAAAAA | 25831 |
rs61995488 | snp | G/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201528 | TTTTTTTTTTTTTTG[G/T]AGGCACGGTCTCACT | 25831 |
rs62806763 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155359 | CAAAAAAAAAAAAAA[A/G]GGAAAAGAGCAACTT | 25831 |
rs66528205 | snp | C/T | 0.41441 | 0.188333 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141010 | TCAGCTCACTGCAAC[C/T]TCTGCCTCCAGGGTT | 25831 |
rs67960414 | snp | C/T | 0.414245 | 0.188477 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141232 | CGTGCCTGGCCTACT[C/T]CTTCTTATATATTTT | 25831 |
rs71112381 | in-del | -/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101525 | GGCCAGGTGTGGTGG[-/G]CTCATACCTGTAATC | 25831 |
rs71112382 | in-del | -/A | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118926 | AAAAAAAAAAAAAAA[-/A]CTACCACAAATTTAT | 25831 |
rs71112383 | in-del | -/A | 0.499759 | 0.0109798 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161871 | GCAGGACTCTGTCTC[-/A]AAAAAAAAAAGAAAA | 25831 |
rs71112384 | in-del | -/A | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187052 | AAAAAAAAAAAAAAA[-/A]CACCCAAAAAACAGG | 25831 |
rs71112385 | in-del | -/TAGATAGATAGATAGA | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188130 | AGATAGATAGATAGA[-/TAGATAGATAGATAGA]CAGACAGATAAAAGC | 25831 |
rs71407681 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190468 | CTGAGTACAAAGCAA[C/T]AAAATGAAAATACCA | 25831 |
rs71417947 | snp | A/G | 0.0182019 | 0.0936463 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100846 | GTCATTAGCATGGTG[A/G]ATCATATACTTCTCT | 25831 |
rs71417948 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119016 | AGAGGCTCTAGAGAA[A/G]AATCTGTTTCCTTGC | 25831 |
rs71417949 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197245 | CACCGTGGCTGGTCT[C/T]GAACTCCTGACCTCA | 25831 |
rs71417950 | snp | C/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200443 | TTAAGCTCAGGAGTT[C/T]TAGATCAGCCTGGGG | 25831 |
rs71427364 | snp | A/C | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177509 | GCAACTGTCTCAAAA[A/C]CAATAATAATAATAA | 25831 |
rs71430920 | in-del | -/A | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131029 | CCCAAAAGATAAACC[-/A]AAAAAAAAAAAAAAA | 25831 |
rs71430921 | in-del | -/A/AAAAAAAAAA/AAAAAAAAAAA/AAAAAAAAAAAAAAAAAA | 0.0528381 | 0.153711 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134042 | GACCCCATTCTCCTT[lengthTooLong]AAAAAAAAAAAAAGG | 25831 |
rs71430922 | in-del | -/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142297 | CTTTAATAAGTATTA[-/G]GGAAAAAACTGGTAC | 25831 |
rs71430923 | in-del | -/A | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142315 | AAAAACTGGTACATC[-/A]AAAACTATTTCATAG | 25831 |
rs71430924 | in-del | -/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142326 | CATCAAAACTATTTC[-/T]ATAGATTACTAAGTG | 25831 |
rs71430925 | in-del | -/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142337 | TTTCATAGATTACTA[-/G]AGTGATATAATGTGA | 25831 |
rs71430926 | in-del | -/A | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142373 | ACTATAATAAATGAG[-/A]AATAAATGCAAATAG | 25831 |
rs71430927 | in-del | -/C | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142415 | AGGGACTATGGGACT[-/C]CATTGAAGTTCCAGT | 25831 |
rs71430928 | in-del | -/C | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142425 | GGACTCATTGAAGTT[-/C]CCAGTGAATTTTTTT | 25831 |
rs71430930 | in-del | -/AC/ACACAC/ACACACACAC | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156516 | TCTCAAAAAAAAAGT[-/AC/ACACAC/ACACACACAC]ACACACACACACACA | 25831 |
rs71430932 | in-del | -/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183711 | TAGTAAAATTTTGTC[-/T]TTTTTTTTTTTTTTT | 25831 |
rs71430934 | in-del | -/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200672 | GTAATTCCAGTTACT[-/G]GGGGCGGCTGAGGCA | 25831 |
rs72111170 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165000 | AAGTCTTGTGTAATT[-/A]AAAAAAAAAAAAAAA | 25831 |
rs72223113 | in-del | -/TAGATAGA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188090 | ATATAGAGACAGCTG[-/TAGATAGA]TAGATAGATAGATAG | 25831 |
rs72670348 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108659 | TGAGAACTTGTCTCT[A/G]TTAAAAAAAAAAAAA | 25831 |
rs72670351 | snp | A/C | 0.361684 | 0.223667 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115177 | GAGATCAATTTTTAA[A/C]CTGTAATAAAAATTG | 25831 |
rs72670356 | snp | C/T | 1.65622e-05 | 0.00287764 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129221 | ACACAGAACTGCTGC[C/T]TCCTTTTCTACTTGA | 25831 |
rs72670359 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140625 | TATAACCTATAACAC[A/G]GTATTACCACTTACG | 25831 |
rs72670360 | snp | A/G | 0.411074 | 0.191194 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140885 | ACCTTTATCAACCCA[A/G]CTTTAGCAATTAGCT | 25831 |
rs72670364 | snp | A/C | 0.27893 | 0.24832 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141758 | TCTTATTAAGAGTTT[A/C]TTTTGTGTGCATAAA | 25831 |
rs72670365 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145789 | CTGATTTCAAATCAA[A/G]AAAGTGAAGCAGTAA | 25831 |
rs72670368 | snp | A/C | 0.126564 | 0.217402 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156550 | ACACACACACACACA[A/C]ACAGATACATGTGTC | 25831 |
rs72670371 | snp | A/G | 0.234109 | 0.249494 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164107 | CAGAGAAAATAACCA[A/G]GCTTTTACAAACTAC | 25831 |
rs72670372 | snp | A/T | 0.0810805 | 0.184299 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165395 | CTCAATCAACACTTG[A/T]CTGTTTCTATTCTCT | 25831 |
rs72670374 | snp | A/G | 0.21875 | 0.248039 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165519 | ATCCTTCTTAAATGT[A/G]AGGTAGAGTCCACGC | 25831 |
rs72670375 | snp | A/G | 0.256619 | 0.249912 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166011 | CTACCATACCCAGCT[A/G]ATTTTTTTATTTTTC | 25831 |
rs72670377 | snp | A/G | 0.21875 | 0.248039 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167282 | CAGCCTGGGCAACGT[A/G]GTGCATCCCCATCTA | 25831 |
rs72670385 | snp | C/G | 0.260983 | 0.253064 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177258 | TGACACCTACAATCC[C/G]AGCACTTTGGGAGGC | 25831 |
rs72670390 | snp | C/T | 0.260714 | 0.251003 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182832 | CTCCAGCCTGGGCAA[C/T]AGAGTGAGACTCTGT | 25831 |
rs72670391 | snp | C/G | 0.21875 | 0.248039 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185310 | CACCACTGCACTCTA[C/G]CCTGGGCGACAGACA | 25831 |
rs72670396 | snp | A/G | 0.21875 | 0.248039 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190127 | CTAGAAGCCAGGCTC[A/G]ACCACATGCAACAGA | 25831 |
rs72670398 | snp | A/C | 0.249132 | 0.249998 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199048 | GAAAAAAAAAAAAAA[A/C]AAAACAGAATCCACA | 25831 |
rs72670399 | snp | A/C | 0.26078 | 0.249767 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205183 | TATCTAGTAAGAATT[A/C]TCTTTTATATTTTTG | 25831 |
rs73257769 | snp | C/G | 0.0792508 | 0.182605 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117780 | TGGCAACAACACTTT[C/G]TCAGAAGATACAAAA | 25831 |
rs73257773 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122737 | ATAAGCAACTTATTT[C/T]CTTTAAGTGGAGAAT | 25831 |
rs73257782 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134737 | TTTTAATGCCTAAAG[G/T]ATCAAGTGATTTGTT | 25831 |
rs73257784 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137458 | TTAGGCCAGGCACAG[C/T]GACTCAGACCTGTAA | 25831 |
rs73257785 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137566 | GTGAGACCTCATCTC[C/T]ACATATTAAAACAAA | 25831 |
rs73257788 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142417 | GGGACTATGGGACTC[A/G]TTGAAGTTCCAGTGA | 25831 |
rs73257791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142558 | CCGCCTCAGAATTAC[A/G]GAAGAGTAGGTGGGA | 25831 |
rs73257794 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149308 | CCAGGCATGGTGGTA[A/C]GCATCTGTAGTCCCA | 25831 |
rs73257797 | snp | A/G | 0.00942921 | 0.0680125 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150254 | TTCAATTAAACATGG[A/G]AAATAATTTCAATTT | 25831 |
rs73259613 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178724 | AGGAGAATCCCTTCC[A/G]GGAGATGGAGGTTGC | 25831 |
rs73259617 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181850 | CCTACATACGTAAAA[C/T]GCACTTTTTTTTATA | 25831 |
rs73265472 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186005 | ACGGTCTGGAATGAG[A/T]ATTTTCTTCAATTTT | 25831 |
rs73265475 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187824 | AGTGCAGTGGCACAA[C/T]CTCATCTCACTGCCT | 25831 |
rs74042156 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112224 | TATCTCTCCTCCTTT[C/G]CTTTGGATTAGTCAT | 25831 |
rs74042157 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116102 | CCAAGAGTCCCAAAC[A/G]CTATTATCTGTTCCT | 25831 |
rs74042159 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121281 | TAGCTCCCTCCTCTC[A/C]CCCCTTCCACACTGC | 25831 |
rs74042160 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121634 | TTTTTCATTAGCCAA[C/G]TTCAGAAAAGTTATG | 25831 |
rs74042161 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123240 | CAACCATAAACTAAA[C/T]CTGAATTACAAAATC | 25831 |
rs74042162 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124279 | CTGACTGATGTCCCT[C/T]TTTTTTTCTCATCTT | 25831 |
rs74042164 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130663 | CATACACACCCATCC[A/G]CACACCCAGATGCTC | 25831 |
rs74042165 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130717 | ATGTTTATGATAGCA[C/T]TCAGAGGGAAATAAT | 25831 |
rs74042166 | snp | C/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134571 | GTGTGTGTGTGTGCG[C/T]GCGTATGTATATACA | 25831 |
rs74042167 | snp | C/T | 0.079617 | 0.182947 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138396 | TTTATATGTGCATTT[C/T]GGTAGTTTTAGACAG | 25831 |
rs74042168 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138434 | ACCAGAGAGCACATT[C/T]CTGGCCTTCCTCTCT | 25831 |
rs74042169 | snp | C/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139642 | ACCTTTTGCCACTTA[C/T]GATCTACGAAATATA | 25831 |
rs74042170 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142225 | CCCAAGTATACAAGA[C/T]GGTTTCAGACTATAT | 25831 |
rs74042171 | snp | A/T | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164069 | TAAAACAAAGTGGAG[A/T]AGTACTCAGTCTAAT | 25831 |
rs74042173 | snp | C/G | 0.079617 | 0.182947 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170667 | AACAAATAGAATTCA[C/G]GCTTGAAGAGACCAT | 25831 |
rs74042174 | snp | C/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176032 | AATGCATCTCTATTT[C/G]GAGTGGCCACATTTG | 25831 |
rs74042181 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194782 | AAGCAATAAAAAAAG[C/G]TTACATGAGGTTCCA | 25831 |
rs74042182 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194924 | AATATAACTGTTTTT[A/T]AAAAAAATAAAGGGC | 25831 |
rs74042184 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198633 | TTTCCACATGACCAA[C/T]GCATAATTTTTGCAA | 25831 |
rs74371023 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112751 | AGTAGCTGGGATTAT[A/T]GGCATGTGCCACCGT | 25831 |
rs74372662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151075 | TCCAGCCTGGGTAAC[A/G]GATCGGGACTCTGTC | 25831 |
rs74381164 | snp | G/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142451 | TTTTTTTTTTTTTTT[G/T]GAGACAGAGTCTCGC | 25831 |
rs74385663 | snp | A/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165001 | AGTCTTGTGTAATTA[A/T]AAAAAAAAAAAAAAG | 25831 |
rs74405564 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181713 | GGTATCAGATTTTAA[C/T]TGTGATCAACTGTGT | 25831 |
rs74422277 | snp | A/G | 0.19334 | 0.243495 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190400 | GAAATCAGAGCCAAA[A/G]GGCAAAAGATCAGGA | 25831 |
rs74440743 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195442 | AACACAATGTCATAC[C/T]CATAAATAAAAATGA | 25831 |
rs74546694 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158109 | ACTCATATAAATGAA[A/T]ATAAGAGATCCTAAT | 25831 |
rs74572565 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185737 | GTTTAAAAAAAAAAA[A/G]AAGATAATTCAACTT | 25831 |
rs74614214 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147934 | ACCAGGCATAGCGCC[C/T]GTAGTCCCAGCTACT | 25831 |
rs74649331 | snp | A/G | 0.010183 | 0.0706243 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168347 | GTGCAAACACTGGCA[A/G]TAACCTTTTCAAGTA | 25831 |
rs74778872 | snp | G/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202668 | CAATCACTTTATTCA[G/T]GGAATAAAGTGCTAA | 25831 |
rs74802027 | snp | C/T | 0.00300272 | 0.0386309 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119916 | AGATGCAAAATTTCA[C/T]TGTTGCAAAAGCAAT | 25831 |
rs74809698 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176274 | AAAAGCAGACAGGAG[G/T]ATCCAGCTGTCTACT | 25831 |
rs74832477 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114476 | GAACTCAAGGAGGAT[C/T]CTTTTTTTCTATATT | 25831 |
rs74852123 | snp | A/G | 0.0182275 | 0.0937096 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141816 | GTATACCAACTGTGT[A/G]AACATTACAAACATC | 25831 |
rs74877659 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167793 | ACAATTTAAATCTCA[A/C]CTCTGCATAAAACTG | 25831 |
rs74908399 | snp | G/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142450 | TTTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTCG | 25831 |
rs74982448 | snp | A/C/G/T | 4.97544e-05 | 0.0049875 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136509 | GAATGCTTATTTCAC[A/C/G/T]GTGCCCTTGCCAGAA | 25831 |
rs74987112 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162565 | AAGGGTTACACTAAC[A/G]TTTCAGATTTTTCTT | 25831 |
rs74991229 | snp | C/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188242 | GTTATTCTTCCTTTT[C/T]TTTTTTTTTTTGAGA | 25831 |
rs75043020 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191626 | CAACTAAAGTAGTAT[A/T]TAAAGAAAAATTTAT | 25831 |
rs75056460 | snp | C/T | 0.00451234 | 0.0472843 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128892 | AGTTAATTCAGATAC[C/T]GAACTAACATCAGGA | 25831 |
rs75096960 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104171 | ATATTTCAAAGAAGC[C/T]AGAAGAGAATAATTT | 25831 |
rs75163321 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122641 | GTGTGGGACTACAGG[C/G]CATGAGCCCTATACC | 25831 |
rs75180670 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157989 | CTATAATCCAAAATA[C/T]AATGCTCTAAGAACT | 25831 |
rs75192944 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120891 | TAAAGTATTAAGAAC[C/T]ATGCTGGCAAGGCAC | 25831 |
rs75194010 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139509 | CAGAATTGTGAGCAA[C/T]GAATTTCTGTTTATT | 25831 |
rs75195475 | snp | C/T | 0.000613716 | 0.0175066 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133365 | AACCTGGGAACGTAC[C/T]AGACGTCTCTGCCGT | 25831 |
rs75208239 | snp | A/T | | | missense | HECTD1 | GRCh38.p7 | 14:31105627 | AGATCCACAGCTGTA[A/T]AACCATATATTCTTG | 25831 |
rs75278274 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137767 | AGAAAAAAAAGAAAA[A/C]AATCCAACAGGAAAG | 25831 |
rs75345169 | snp | C/T | 0.00635585 | 0.0560136 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129095 | ATGAAAGAACAACAA[C/T]TGGTTCATGGACATC | 25831 |
rs75385127 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170627 | CCCTTAGAAGCATCA[C/T]TCTCTCTAAAAACTA | 25831 |
rs75396964 | in-del | -/TTCTC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139606 | ATAAGAGGAACCCTT[-/TTCTC]AGCTTTTTCCACTGA | 25831 |
rs75494061 | snp | A/G | | | missense | HECTD1 | GRCh38.p7 | 14:31105624 | TTGAGATCCACAGCT[A/G]TAAAACCATATATTC | 25831 |
rs75549019 | snp | A/G | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134968 | CAATTTCTCAGTGCA[A/G]ACCTTCCATAACCAC | 25831 |
rs75558116 | snp | A/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181182 | TACATCAAAAAAAAA[A/T]TAAAATTTAAGAGCA | 25831 |
rs75585150 | snp | A/G | 0.00288251 | 0.0378543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148842 | AGCTTACTTTGTTAC[A/G]ATTTAACATATTCAT | 25831 |
rs75588246 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177611 | CTTAAAGTGCTTAGA[A/G]TAATGTCTAGCACTG | 25831 |
rs75665643 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123857 | TTCAGTGCCTTTTAC[G/T]GGATGGCCAGTAGAA | 25831 |
rs75674417 | snp | A/C | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125575 | GAGGGGCACAGGGCC[A/C]CCATGAGAAATAATA | 25831 |
rs75784286 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167334 | ATGGTGGCATACTTG[C/T]AGTCTCAGCTATTCG | 25831 |
rs75794036 | snp | G/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125189 | TTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTT | 25831 |
rs75818702 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155953 | ATTTTTTTTTTTTTA[A/G]GATGGAGTCTCAGGC | 25831 |
rs75836875 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193034 | AGCATTAGATAACCT[A/G]GATAATCCTATATCT | 25831 |
rs75846389 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147670 | CCGAGGTTCAGGCAA[C/T]TCTCATGCCTCAGCC | 25831 |
rs75854791 | snp | C/T | 0.220246 | 0.248223 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178755 | AGTGAGCCGAGATTA[C/T]GCCACTGTACTCCAG | 25831 |
rs75858941 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130150 | ATTTCTTACAATTTG[C/G]GCTAACCTCTCAAAA | 25831 |
rs75896482 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202008 | CAGTGGAGAGCCGGC[C/T]GGGCGCGGTGGCTCA | 25831 |
rs75921052 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122788 | CTGCTTTTCTTAATT[A/G]ACTACATTTTTTATA | 25831 |
rs75954571 | snp | A/C | | | missense | HECTD1 | GRCh38.p7 | 14:31107672 | CTCTAATGTGGGTCC[A/C]AAGCCAGTTCCTTCT | 25831 |
rs76031682 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155845 | ATTTTCTGATTAGTA[C/T]GATTTTGATAATTAT | 25831 |
rs76054092 | snp | G/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195538 | AACTTTTTTTTTTTT[G/T]GAGACAAGGTCTCAC | 25831 |
rs76096610 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125353 | CTAATTTTTTGTACT[C/T]TAGTAAAGAGGGTTT | 25831 |
rs76107409 | snp | G/T | 0.040671 | 0.13668 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139704 | ATTTTCCAGTGATTT[G/T]ATCAAACAAAACAGA | 25831 |
rs76171104 | snp | A/C/T | 0.00181558 | 0.0300756 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113840 | CAAAGCACGAAGCCA[A/C/T]TTGCAATCAAAATAG | 25831 |
rs76187544 | in-del | -/AA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131042 | CCAAAAAAAAAAAAA[-/AA]TAGAGTCAGTAATGA | 25831 |
rs76212190 | snp | A/C | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156505 | AGCGAAACTCCATCT[A/C]AAAAAAAAAGTACAC | 25831 |
rs76230034 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102036 | GAAATAGTAAATGAA[C/T]GACATGCCACAACAT | 25831 |
rs76238671 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131303 | AAACAAAAAACACTC[A/C]AAATATTCAGATGTA | 25831 |
rs76272797 | snp | A/C | 0.00149063 | 0.0272598 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148762 | ATTTCAGTTTTCTGC[A/C]TCTTTTGCCAGTCCA | 25831 |
rs76309595 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205295 | TACTCTTCTGCTACA[C/T]GGTTAAGATCCAATT | 25831 |
rs76319316 | snp | A/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147656 | CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 25831 |
rs76341127 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187807 | TCTCACTCTATCACC[A/G]GAGTGCAGTGGCACA | 25831 |
rs76399276 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154745 | CCCCAGTAATTCTGA[C/T]GATTAAACAGATTTG | 25831 |
rs76420252 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161491 | GCAAGAGGATACACT[A/G]TGCCATGGAATTCAA | 25831 |
rs76447932 | snp | G/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148154 | AAATGAAAAAAAAAA[G/T]GCAAGAACAATAAAC | 25831 |
rs76476839 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187547 | ACAGCATGAGCAAAG[C/T]GAACAGGACATTTGT | 25831 |
rs76507700 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162398 | GATACTCCAGTACCA[C/T]TTAATAAATAGTACC | 25831 |
rs76529923 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147978 | CAGGAGGATTACTTG[C/T]ACTCAGGTATTTTAG | 25831 |
rs76531177 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162795 | TGTTTTAAAAAAAAA[A/T]TTGGGCCAGTCGCAG | 25831 |
rs76567512 | snp | A/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131248 | TTCTAGGCTAGGTGA[A/T]TTTTTTTTTTCCCAT | 25831 |
rs76599182 | snp | A/G | 0.0107246 | 0.0724382 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208610 | CTCAGGCAACCAGAG[A/G]AGCTGCTAGGTATGA | 25831 |
rs76777949 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126138 | GTTATAGAAACCCAT[C/G]CAACATATGTGAAAA | 25831 |
rs76795460 | snp | C/T | 0.02016 | 0.0983543 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119301 | TACCACAATCTAAAA[C/T]AGAGTTTTGTAAGGG | 25831 |
rs76869948 | snp | G/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102445 | TTTTTTTTTTTTTTT[G/T]TGAGACAGAGTTTCA | 25831 |
rs76899140 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155944 | TTACCATCAATTTTT[G/T]TTTTTTTAAGATGGA | 25831 |
rs76905212 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152885 | CAGCTACTTGGGAGG[A/C/T]TGAGGCAGGAGAATT | 25831 |
rs76977568 | snp | A/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182866 | AGAAATTAATAATTA[A/T]AAAAAAAAAAACTCA | 25831 |
rs77031367 | snp | G/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181915 | TCTTTTTTTTTTTTT[G/T]GACAGTCTCGCTCTG | 25831 |
rs77089622 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197697 | TCACTCTCTTTCTTA[C/T]CTCTTTGACCTTTAA | 25831 |
rs77306640 | snp | A/G | 0.079617 | 0.182947 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170183 | TTGGGAGGCTACACC[A/G]GAGGATCACTGGAGG | 25831 |
rs77379613 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192718 | TGGTGGTTCATGCCT[A/G]TAATCTCAGCACTTT | 25831 |
rs77407218 | snp | C/G | 0.00238814 | 0.0344727 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106204 | TAACCTAAAATCACA[C/G]CTGAAGATATGATAA | 25831 |
rs77463721 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188789 | TCCAGAATGAGAAGC[C/G]AAATGAAAAGAATTC | 25831 |
rs77536624 | snp | C/T | 0.0100197 | 0.0700675 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168285 | TAACACATCAAATAG[C/T]ATGAATAACTACCTT | 25831 |
rs77562000 | snp | A/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181183 | ACATCAAAAAAAAAA[A/T]AAAATTTAAGAGCAA | 25831 |
rs77587141 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200794 | CTTGAAAAAAAAAAA[A/G]AGAAAAACCACTTCC | 25831 |
rs77596468 | snp | C/T | 0.00347052 | 0.0415117 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106266 | AAAAGTTCTGCAGCA[C/T]CTCAACTGCTACAGC | 25831 |
rs77599558 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195090 | TCCATTTCATATTCC[A/C]TTTTTGCCTCTGCTC | 25831 |
rs77622354 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114651 | TGTTAATTTGTTAAA[C/T]ATAAGGCAAAGTAGC | 25831 |
rs77633158 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185736 | TGTTTAAAAAAAAAA[A/G]GAAGATAATTCAACT | 25831 |
rs77638332 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202530 | AGTCCTATTTGCTAC[A/T]ACTTTATGAAATCAA | 25831 |
rs77654935 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114862 | ACGTAGGCTATGTGT[C/T]ATAGCCTATTTTTCC | 25831 |
rs77698356 | snp | A/C/G | 3.31763e-05 | 0.00407272 | synonymous-codon, missense | HECTD1 | GRCh38.p7 | 14:31105626 | GAGATCCACAGCTGT[A/C/G]AAACCATATATTCTT | 25831 |
rs77707759 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198240 | CTGCATACGGAAGAA[A/T]AATGGCAAAGTACAT | 25831 |
rs77723326 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148136 | TATCTTACTTTTTTT[A/T]AAAAATGAAAAAAAA | 25831 |
rs77729159 | snp | A/C | 0.0573587 | 0.15934 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147809 | AAAAAAAAACAGAAA[A/C]ATCATTATTACAATT | 25831 |
rs77755935 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125837 | AAACTTTGTCTTTAA[A/G]ATTACTCCCAATTTT | 25831 |
rs77772672 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182646 | CACTTGAGCTAAGGA[C/G]TTCGAGCCCAGCCTG | 25831 |
rs77779690 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128338 | AGTCATCTATTTCCT[C/G]ATGCAACTTTGCTTA | 25831 |
rs77896262 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130629 | GTTCTTACCCATACA[A/T]AAAAGGGGCCCAAGA | 25831 |
rs77991036 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148242 | AAAATTAGTCAATTA[G/T]GCATCTGCTACTGTA | 25831 |
rs78030840 | snp | A/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121980 | CAAATTTTTTTTTTT[A/T]ATGCCTCTACTTCAT | 25831 |
rs78081376 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118473 | TTAACTACCTTGTCA[A/G]ACAGGGACCTTTATT | 25831 |
rs78158420 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179735 | ATGTGACATCAAATA[C/T]ATTATTCTAGTTTCT | 25831 |
rs78233461 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121943 | GGGTCCTCACTCTTC[C/T]ACTTAACTCTGATGA | 25831 |
rs78253385 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142731 | CAGGCACGAGCCACC[A/G]CGCCCAGCCTAAAGT | 25831 |
rs78270146 | snp | C/G/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201526 | TTTTTTTTTTTTTTT[C/G/T]GGAGGCACGGTCTCA | 25831 |
rs78328350 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134520 | TGTGTATGCATAAAT[A/G]TGTGTGTGTGTGTGT | 25831 |
rs78340878 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189963 | GACTTCAAATGCTAA[C/T]TCAATGAACAAGATG | 25831 |
rs78432707 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139718 | TGATCAAACAAAACA[A/G]ACTTCAAGTCATTAA | 25831 |
rs78463451 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144716 | CCATAATTTGCTGAC[C/T]CCCTACTCAATACCC | 25831 |
rs78509051 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180955 | TGCATATGTAGTAGA[C/T]GGAAGAAATGAAAAG | 25831 |
rs78546823 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147920 | AAAACTATCTTAGAA[C/T]CAGGCATAGCGCCTG | 25831 |
rs78567120 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184697 | AGTGAGCCATGATCA[C/T]GCACAATGCACTTTA | 25831 |
rs78571955 | snp | A/C | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192336 | GCGAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 25831 |
rs78666509 | snp | A/C | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192337 | CGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 25831 |
rs78945950 | snp | G/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158269 | TTTTTTTTTTTTTTT[G/T]TTTGGAGACAGAGTC | 25831 |
rs79019297 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114656 | ATTTGTTAAACATAA[C/G]GCAAAGTAGCAGAAA | 25831 |
rs79043885 | snp | G/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159658 | TTTTTTTTTTTTTTT[G/T]GAGACAGGGTCTTGC | 25831 |
rs79044485 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114205 | CCCTTCAACGTTCAA[C/T]TGCAATACTGTGTTA | 25831 |
rs79050267 | snp | G/T | 0.030278 | 0.119257 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132868 | AAAATGTTAATCCTT[G/T]TTCTTCTATATGATT | 25831 |
rs79068796 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161265 | AAATTTAAAAGGACA[C/G]ATTTGGCTAATGCAA | 25831 |
rs79075358 | snp | C/G | 0.0524604 | 0.153226 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208698 | TACTCTCTTGAGGCC[C/G]GGAGTTCGAGACCAG | 25831 |
rs79114561 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192633 | GAATATCACAAACAA[C/T]TCTATGCCCATAAAT | 25831 |
rs79129806 | snp | A/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108662 | GAACTTGTCTCTATT[A/T]AAAAAAAAAAAAAAG | 25831 |
rs79165598 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205618 | TCAGTCCTAGAGTTT[C/T]TTCACCTACCAATTT | 25831 |
rs79240866 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160066 | TATATGTTATTTATC[C/T]ATCTCTCTCTCGTAT | 25831 |
rs79243914 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167801 | AATCTCACCTCTGCA[C/T]AAAACTGTCTCCAAT | 25831 |
rs79253184 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202338 | AAGGCTATCACACAA[C/T]TATTCAGTGGAAAAG | 25831 |
rs79370921 | snp | A/C | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192335 | AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 25831 |
rs79379382 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153902 | ATATGCTATTGGCTT[G/T]TTCATTTTTTGAAAA | 25831 |
rs79436578 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117677 | TGGACATAATTAAGG[A/T]CATTTCCAATTTTTT | 25831 |
rs79537871 | snp | A/C | 0.496314 | 0.0427728 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149443 | ACACTGTCTCCAAAA[A/C]AAAAAAAAAAAAAAA | 25831 |
rs79543266 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113783 | TTTAAAATTATGTCT[C/G]AATGAACTGCTGTTC | 25831 |
rs79553811 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172675 | TCTTAAAAATAAACA[C/T]GAAATAACAAAGGAA | 25831 |
rs79636592 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104829 | AGGCACGTGCCACCA[C/G]ATCTAGCTAATTTTT | 25831 |
rs79640126 | snp | A/G | 0.0344966 | 0.126721 | synonymous-codon, intron-variant | HECTD1 | GRCh38.p7 | 14:31113967 | GCGCAGGAAAGCAGC[A/G]TCTGCATTCTTCTGC | 25831 |
rs79640381 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179532 | TAAAAACAGCTCAGT[A/G]CCTAGCATATTAAAC | 25831 |
rs79673976 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155681 | CAGGACAAACTATCG[C/T]AGGTTCTCAGGAATA | 25831 |
rs79683658 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148356 | TTGCTGTATCACAAG[A/G]TATTAACCCAGATTG | 25831 |
rs79689004 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134626 | ATATTCACAGCATCT[C/G]AGCCTTTTGGCTAAG | 25831 |
rs79698141 | snp | A/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155951 | CAATTTTTTTTTTTT[A/T]AAGATGGAGTCTCAG | 25831 |
rs79740359 | snp | A/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178825 | AAAAAAAAAAAAAAA[A/T]TTCAGCGCTCACCTC | 25831 |
rs79766859 | snp | C/G | 0.0788843 | 0.182262 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184240 | GATCACTTGAGCCCA[C/G]GATTTCTAGACCAGC | 25831 |
rs79787488 | in-del | -/TT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177916 | AGAAATTTTTTTTTT[-/TT]AGTAAATACATTTTT | 25831 |
rs79814511 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129788 | GACATTTAAAAGCAA[C/T]GTAAGGGTCATGTTT | 25831 |
rs79845028 | snp | C/T | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127907 | GTTGCTGTAGCTACA[C/T]TGCTGCTGCTAGTAA | 25831 |
rs79864592 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142863 | CAAGGAAGGCAGATC[A/G]CTTGAGCCCAGCCTA | 25831 |
rs79893321 | snp | A/C | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103544 | TGAGACTCCGTCTCA[A/C]AAAAAAAAAAGAATG | 25831 |
rs79911084 | snp | A/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181621 | CCCTGTCTCAAAAGA[A/G]AAAAAAAAAAAAACA | 25831 |
rs79913218 | snp | A/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131247 | TTTCTAGGCTAGGTG[A/T]TTTTTTTTTTTCCCA | 25831 |
rs79940834 | in-del | -/AAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155357 | CTCAAAAAAAAAAAA[-/AAA]GGAAAAGAGCAACTT | 25831 |
rs80002178 | snp | G/T | 0.0410537 | 0.137264 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100525 | GGATTTTTGACCAAG[G/T]AGCTTAAAAGCCAGC | 25831 |
rs80046220 | snp | A/C | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155346 | CAAGATACCGTCTCA[A/C]AAAAAAAAAAAAAGG | 25831 |
rs80091686 | snp | A/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199033 | AGAATCTGCCTCGAA[A/G]AAAAAAAAAAAAAAA | 25831 |
rs80130235 | in-del | -/TT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177899 | GAAGAATTTTTTTTT[-/TT]AGAAATTTTTTTTTT | 25831 |
rs80140861 | snp | G/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195539 | ACTTTTTTTTTTTTT[G/T]AGACAAGGTCTCACT | 25831 |
rs80187356 | snp | G/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127851 | ATGTGAGGCTGGTGG[G/T]TAAAGTGTTACTTAA | 25831 |
rs80257408 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146701 | CTACTAAAAATGCAA[A/C]AATGAGCCGGGCATG | 25831 |
rs80310064 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199035 | AATCTGCCTCGAAGA[A/G]AAAAAAAAAAAAAAA | 25831 |
rs80311567 | snp | A/G | 0.117537 | 0.212022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177721 | CTAAGTGACTACCAG[A/G]AACTGAAGTGCACTG | 25831 |
rs111372129 | snp | A/G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31168997 | TGCAGTGAGCCGAGA[A/G/T]AGCGCCATTGCACTC | 25831 |
rs111396640 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159794 | ACAGGCTCCTGCCAC[C/T]GTGCCCAGCTAATTT | 25831 |
rs111420937 | snp | G/T | 0.444444 | 0.157135 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144600 | TCATGTGTCTTGAAA[G/T]TGTCCTTCTGGTTTG | 25831 |
rs111428624 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149776 | GGCATGGTGACAGGT[A/G]CCTGTAGTCCCAGCT | 25831 |
rs111482376 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187357 | AGTGAGACTTTCTCA[A/T]AAATAAAATAAAAGT | 25831 |
rs111501626 | snp | A/G | 0.0187042 | 0.0948803 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148713 | TAAAGCACATCCAAC[A/G]GATATACCTTTTGCT | 25831 |
rs111507761 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163490 | CAACTGTGGTCGCAA[A/G]TGGTTGGGAGGCTGA | 25831 |
rs111516164 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161718 | AGATGAGGAGTTCGA[G/T]ACCAGCCCAGCCAAC | 25831 |
rs111547023 | in-del | -/T | 0.420415 | 0.182917 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124810 | TCATCTAACAATAAA[-/T]TTTTTTTTTTTTTTT | 25831 |
rs111561998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132296 | TACAAAATTAGCCAG[A/G]CATGGTGGCCCATGC | 25831 |
rs111610541 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103964 | AAGAGCAAAAACTCC[A/G]TCTCAAAAAAACAAA | 25831 |
rs111625196 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125560 | TAACAAATCAGTAGA[C/G]AGGGGCACAGGGCCA | 25831 |
rs111631349 | snp | C/T | 0.26818 | 0.249338 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116691 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 25831 |
rs111657176 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182439 | CTCAAGCAATCTGTC[C/T]ACCTCAGCCTCCCAA | 25831 |
rs111683057 | snp | A/G | 0.00334796 | 0.0407771 | missense | HECTD1 | GRCh38.p7 | 14:31103045 | CTTAATTTCTCCATT[A/G]GAAAAACTTTATTAA | 25831 |
rs111694201 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184545 | GTGAGCCAAGATCAC[A/G]CCACTGCACTCTAGC | 25831 |
rs111732800 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112806 | GTAGAGACTGGGTTT[C/T]GCCATATTGGCCAGG | 25831 |
rs111838734 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139702 | TCATTTTCCAGTGAT[A/T]TGATCAAACAAAACA | 25831 |
rs111861145 | snp | C/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166517 | AGAAGCTATGAAGGG[C/T]TCAAACTAGGCAGTC | 25831 |
rs111877661 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142454 | TTTTTTTTTTTTTGA[C/G]ACAGAGTCTCGCTCT | 25831 |
rs111914609 | snp | A/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104156 | AGTTAACAATAATAT[A/T]TATTTCAAAGAAGCT | 25831 |
rs112013019 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157379 | TGCATTAATGAACAG[C/T]AAAATATCCAATGTT | 25831 |
rs112013919 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163087 | CACACACGCACACAC[A/G]CACACACGCACACAT | 25831 |
rs112052455 | snp | C/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179101 | CTGTTTCCTTACTTA[C/T]AAAGCATAAGTAATA | 25831 |
rs112065814 | snp | C/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139447 | AGGAATAGGCCCTCA[C/T]GAGACACCAAATCTG | 25831 |
rs112065855 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148138 | TCTTACTTTTTTTTA[A/C]AAATGAAAAAAAAAA | 25831 |
rs112127200 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168206 | CCTTTTTAACATTAA[A/C]ATAAACCTCAAATAC | 25831 |
rs112146900 | snp | A/T | 0.000218614 | 0.0104527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102880 | ATTTGGGGAATATAA[A/T]TAATTTTGTTGATCT | 25831 |
rs112157479 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147700 | GAGGCAGAGGTTACA[A/G]TGAGCTGAGACTGCA | 25831 |
rs112174347 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170705 | AGGCTAGAAAGCTAC[A/G]AACCTGTTATTGAAA | 25831 |
rs112195237 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158299 | CTCGCTCTGTTGTCT[C/T]GGCTGGAGTGTAGTG | 25831 |
rs112206565 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161836 | AGATGGCGCCACTTC[A/G]CTCCAGCCTGTGCAA | 25831 |
rs112242799 | in-del | -/GTGT | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122264 | TTCATACACACACAC[-/GTGT]GTGTGTGTGTGTGTG | 25831 |
rs112265119 | in-del | -/AAAA | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184956 | GTTCACATTGAAACT[-/AAAA]AAAATAACAAGTGTC | 25831 |
rs112279952 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176486 | AAATAGACAAAACCT[A/G]TATGAACAAAAGCTC | 25831 |
rs112315361 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181619 | GACCCTGTCTCAAAA[A/G]AAAAAAAAAAAAAAA | 25831 |
rs112447297 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137535 | CTAGGAGTTCAAGAC[C/T]GGCCTGGGCAACACA | 25831 |
rs112499455 | snp | A/T | 0.0818113 | 0.184966 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127311 | TCTCGTATTACTGAG[A/T]TTTTTCATATTATAT | 25831 |
rs112501472 | snp | A/G | 0.137527 | 0.223271 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156164 | AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG | 25831 |
rs112531031 | snp | C/T | 0.119281 | 0.213102 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187305 | GGAAGGGGCAGTGAG[C/T]CAAGATCACGCCACT | 25831 |
rs112597428 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134655 | AGATACAGTGTAAAA[C/T]AGCTCGGCTTTCTAT | 25831 |
rs112609224 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198809 | TCCAGTACTTTGGGA[A/G]GCCAAGGCAGGTGCA | 25831 |
rs112611532 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118098 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTTC | 25831 |
rs112680954 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123738 | CAAAATACTTTATAT[A/T]CCTGAAGAACATCCA | 25831 |
rs112716061 | snp | A/C | 0.235854 | 0.249599 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186970 | GGAGGTTGCAGTGAG[A/C]CGAGATCGCACTACT | 25831 |
rs112721397 | snp | C/G/T | 0.0418186 | 0.138422 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127128 | AGGCAACCGCCACCA[C/G/T]GCCCAGCTAATTTTT | 25831 |
rs112760574 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154336 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTA | 25831 |
rs112788358 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103415 | GGCGTGGTGGCGGCT[A/G]CCTGTAGTCCCAGCT | 25831 |
rs112796510 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122319 | CTGGAGTGCAGTGAC[A/G]CAATTATAGCTCACT | 25831 |
rs112803741 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166715 | ACATTAGCTGGTGTG[A/G]TAGTGCATGCCTGTA | 25831 |
rs112848628 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186775 | CTCATGTCTGTAATC[C/T]TAGCACTTTGGGAGG | 25831 |
rs112873209 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105239 | CTCCCAACCTCAGGT[A/G]ATCCTCCCGCCTCAG | 25831 |
rs112930614 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132501 | ATATATATGTGGTGT[A/G]AGTTGAGAATATAAA | 25831 |
rs112960898 | in-del | -/T | 0.228253 | 0.249052 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165853 | TCAGAGAGTGAAACC[-/T]TTTTTTTTTTTAGAT | 25831 |
rs112975011 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193185 | TCCTATGTTTTCTTC[C/G/T]AGAAGTTTTATAGTT | 25831 |
rs112997139 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103392 | CTAAATATACAAAAA[A/C]TTAGCCGGGCGTGGT | 25831 |
rs113005543 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158216 | GCTTAGACCGTAGCA[A/G]ACACTCAATAAAGTC | 25831 |
rs113053812 | snp | A/C/T | 0.0217236 | 0.101931 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192832 | AACGCAAAAAATTAG[A/C/T]CGGGTGTGGTGACAG | 25831 |
rs113056150 | snp | C/T | 0.219049 | 0.248077 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187156 | AGTTCGAGACCAGCC[C/T]CGCCAATGTGGCAAA | 25831 |
rs113274975 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182094 | GAATGGGGTTTCACC[A/G]TGTTGGCCAGGCTGA | 25831 |
rs113318973 | snp | C/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138161 | TGGACTAGGAATGCT[C/G]AATCGGTAACAAATA | 25831 |
rs113389811 | snp | C/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142585 | GGGACTACAGGTGCA[C/T]GCCAACACGCCTGGC | 25831 |
rs113396607 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156033 | CGGGCGGATCACGAG[A/G]TCAGGAGATCGAGAC | 25831 |
rs113409882 | snp | A/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140316 | AGTTTTGAAAAAATA[A/T]TTGATGGCTAGGGTA | 25831 |
rs113419701 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182490 | GAGCCACTGTGTCCA[A/G]CCAATATTCCTATTA | 25831 |
rs113456714 | snp | A/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156955 | AATATATCACCACCT[A/T]TATCTACTAAATCCC | 25831 |
rs113481672 | snp | A/G | 0.317692 | 0.240661 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31210046 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGTTCTGTT | 25831 |
rs113482323 | snp | C/T | 0.213937 | 0.247385 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182442 | AAGCAATCTGTCCAC[C/T]TCAGCCTCCCAAAGT | 25831 |
rs113515565 | snp | C/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154915 | TGCTGGGAACCACTA[C/G]ACACAGAAAAGGTAT | 25831 |
rs113532232 | snp | C/T | 0.216048 | 0.247684 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203768 | TTTTTTTTTATTATA[C/T]TTTAAGTTTTAGGGT | 25831 |
rs113608521 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152929 | AGGCAGAGGTTGCAG[G/T]GAGCCGAGATCACGC | 25831 |
rs113700306 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178617 | GACCAGCCTGCCCAA[C/T]ATGGCGAAACCTCAT | 25831 |
rs113710551 | snp | A/T | 0.5 | 0 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099866 | ATCTGGTGTTTTTTT[A/T]AAAAAATAACACAAG | 25831 |
rs113745623 | snp | A/G | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199607 | GTAATCCCAGCTACT[A/G]GGGAGGCTGATGCTG | 25831 |
rs113905015 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188036 | GATGGTATTACAGGC[A/G]TGAGTCACCACACCT | 25831 |
rs113975390 | snp | C/T | 0.5 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188138 | AGATAGATAGATAGA[C/T]AGATAGACAGACAGA | 25831 |
rs114039582 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160753 | TCAGCTCACTGCAGC[C/T]TCGACCGCCCAGGCT | 25831 |
rs114091356 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143950 | ATTCATTTGGCTCAA[A/G]CTAATCATAAAACCT | 25831 |
rs114115418 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115663 | TACTCAGGGGACTGA[A/G]GTGGGAAAATCACCT | 25831 |
rs114152935 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122318 | GCTGGAGTGCAGTGA[C/T]ACAATTATAGCTCAC | 25831 |
rs114229327 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114215 | TTCAACTGCAATACT[A/G]TGTTAGTTTTACTAT | 25831 |
rs114260346 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115305 | ATTACTTTTATTGGC[C/T]ATTACATAAGATTAT | 25831 |
rs114317326 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109217 | CTAACCCCTAAGGAG[A/G]TGGACTGACATCCTC | 25831 |
rs114339652 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184457 | GCCAGGCATGGAGGC[A/G]TGCACCTGTGGTCCC | 25831 |
rs114357288 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201301 | TAAGTGACATCATTA[C/T]TTTTTAAATAAAGCC | 25831 |
rs114464998 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105301 | CCACCGTGCCCAGCC[A/G]ACCACCAGCAATTCT | 25831 |
rs114480460 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146891 | CAAATAAGGTGTCTT[A/T]AAACAAAAACATACT | 25831 |
rs114581209 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126682 | AGATAATTGCAATTT[A/T]AAAAAAAATATTTTT | 25831 |
rs114585656 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192716 | CGTGGTGGTTCATGC[C/T]TATAATCTCAGCACT | 25831 |
rs114587760 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165310 | TCTAACTGGTCACCA[A/T]TCCCTATACAACCCA | 25831 |
rs114652405 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145979 | CCCTCACTCCACACC[C/T]TCCATAATTTTTTTT | 25831 |
rs114777913 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126897 | CTGGTCTTGAGTTCC[C/T]GAGCCTCAGGTGATC | 25831 |
rs114778661 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160879 | TTTCACTAGTTGCCC[A/C]GGCTGGTCTCAAACT | 25831 |
rs114785361 | snp | C/T | 0.00100867 | 0.0224348 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121555 | ATTATTTGACCCATA[C/T]ATGCCCCCTTTCAGC | 25831 |
rs114937301 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200094 | CCAGTGTTCTCTCTC[A/T]GTGAGTGGCATCATC | 25831 |
rs114977675 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140896 | CCCAGCTTTAGCAAT[G/T]AGCTACTAATGGCCA | 25831 |
rs114993689 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120059 | AAGTTGCATCAGTGA[C/T]GGTTATACAAATCTA | 25831 |
rs115013782 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203756 | ATGGCAACACTTTTT[A/T]TTTTTATTATACTTT | 25831 |
rs115061002 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122229 | AGCTAACTGCAGCAC[A/G]AGCCACTGCACTGGC | 25831 |
rs115074474 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177461 | TTGCAGTGAGTCAAC[A/G]TCGTGCCACTACACC | 25831 |
rs115107117 | snp | A/G | 0.00166077 | 0.0287685 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31112424 | TTCTTACCTTGAGGC[A/G]CCAAATGCTGTACAT | 25831 |
rs115170254 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198766 | ATTATAACTAATCCT[A/G]GTAGGGTGCAGTGGC | 25831 |
rs115229960 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111584 | TTATGCATGAATTCA[C/T]AGAGAAGAGGTTCCA | 25831 |
rs115294525 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189640 | GGTGGTGTATGCCTA[C/T]AGTCCCAGCTACCGG | 25831 |
rs115295346 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140236 | CAGATGTATGATTTA[C/T]TTTTAAAGTTTAAAT | 25831 |
rs115305119 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140290 | AAATAAAAAAGAATA[C/T]AAAGCAACAAAGTTT | 25831 |
rs115334262 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119096 | GTCACTCTGACTCCT[A/G]TTTCCTTAGTCACAT | 25831 |
rs115354883 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123792 | AAACTTACACCTGCA[G/T]ACCACTGAACCAAAT | 25831 |
rs115412889 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105027 | TTTTTTTTGTGCAGC[A/G]GAGTTTTGCTCATCG | 25831 |
rs115453862 | snp | C/T | 0.00165801 | 0.0287447 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140041 | TTTTGTATAACTACA[C/T]GTAAATGTTCATGCA | 25831 |
rs115474143 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192805 | ACATGGTGAAATTCC[A/G]TTTCTACTAAAAACG | 25831 |
rs115480019 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124562 | CTCACTTATAAGTAG[A/G]AGCTAAACCTTGGGT | 25831 |
rs115481932 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155968 | AGATGGAGTCTCAGG[C/T]CGGGTGCGGTGGCTC | 25831 |
rs115491644 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166032 | TTTATTTTTCATAGA[A/G]ACAGGGTTTCGCCAC | 25831 |
rs115495196 | snp | G/T | 0.000865599 | 0.0207858 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107551 | ACTCAAGTCACAAAA[G/T]GAGAAATATTCTTAC | 25831 |
rs115527386 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147712 | ACAGTGAGCTGAGAC[A/T]GCACCATTCTACAGT | 25831 |
rs115562415 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105803 | ACATGGCTATCAAAA[A/C]CATAAATCCCACCCC | 25831 |
rs115571971 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174647 | CAAGTCAGCAAAATT[A/G]CACTCAGTACAAGTA | 25831 |
rs115606930 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208919 | ATTTGTCATTTCCAA[A/G]ATACTGGTTCTTTTT | 25831 |
rs115720519 | snp | A/G/T | 0.0283406 | 0.115616 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208679 | TCCCAGCACTTTATG[A/G/T]TTTTACTCTCTTGAG | 25831 |
rs115848829 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201370 | CCAGAGGACATAACT[C/T]TCAAATTATATTCAG | 25831 |
rs115851472 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197706 | TTCTTATCTCTTTGA[C/T]CTTTAAAAGAAAAAA | 25831 |
rs115857095 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171796 | GAAATAAAAGGTTTT[A/G]TATCATTCTAATTTT | 25831 |
rs115895145 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111637 | GGTTTTCACACAGCG[C/T]GCTTCTCTGGGTGGA | 25831 |
rs115923390 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164591 | ACTATCCTCACCTTG[A/G]AGACGAGCCAATTGA | 25831 |
rs115925975 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204661 | TAAAAAATCTACTTT[A/G]CTATAAATCCTGCTA | 25831 |
rs115953114 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132142 | TTCTAGCTCTTTAAA[C/T]ATGTGGTGTAAGTTG | 25831 |
rs115995357 | snp | C/T | 0.0543475 | 0.155628 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208210 | TAAGGAAGGCGTCTC[C/T]CCCCGCTCCTGGGAG | 25831 |
rs116029264 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124951 | AAGCTGGGACTACAG[A/G]GATCCGCCACCACAC | 25831 |
rs116077910 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161158 | ACCTGCTGGCAAATT[A/T]TTTTAGATTAAAAGT | 25831 |
rs116095613 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159774 | CCTCCCAAATAGCTC[A/G]GACTACAGGCTCCTG | 25831 |
rs116217697 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157843 | TCAGGAGCCTGAGGC[A/G]GAATAATCACTTGAA | 25831 |
rs116236553 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122763 | AGAATCATAAATGCT[C/G]AGATTAAAACTGCTT | 25831 |
rs116270889 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153974 | CAATTGGCCATATGT[A/G]TAGTGGGTCATTCAT | 25831 |
rs116320599 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193115 | CTCTTATGAATTGTG[C/T]TTTTGGTGCTTATCT | 25831 |
rs116354310 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168029 | CTTCTAAAAAGCTCA[A/G]TAAGTGGTTGCAATA | 25831 |
rs116393088 | snp | A/T | 0.0811548 | 0.184367 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199755 | CAACTTCCCAGTTTC[A/T]TTCTGAATATGGCAA | 25831 |
rs116395370 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141557 | GATGACATCACTGTA[C/T]TCCAGCCTGGGCAAC | 25831 |
rs116444920 | snp | A/C | 0.030278 | 0.119257 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117209 | TGAACCCCGTCTCTA[A/C]CAAAAATGCAAAAAT | 25831 |
rs116479617 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144443 | AGGGCCCAGTGCAAA[C/T]AGTTTAGGCTTTGCA | 25831 |
rs116511351 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192207 | AAAAATTAGCCGGGT[A/G]TGGTCTTGAGCGCCT | 25831 |
rs116566634 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104452 | GCTTAACATCACAAA[C/T]GTGAACAGAGAGAGA | 25831 |
rs116617093 | snp | A/C | 0.000140321 | 0.00837502 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106232 | TAATTACCTGTACAT[A/C]AAGTAACAGAGTTTT | 25831 |
rs116634399 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127266 | AGGTGTGAACCACCG[C/T]ACCTGGCCCCAGATA | 25831 |
rs116634475 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188181 | TGTGTGCTGTTCCAT[C/T]TGTCTAAAATCCTTT | 25831 |
rs116720715 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31123562 | CTTGCCTTCGATGGA[A/G]ACTGGGTCAAATTAC | 25831 |
rs116792456 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147733 | ATTCTACAGTTTGGG[C/T]ATCAAGAGCGAAACC | 25831 |
rs116814765 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196821 | TAAGGAAAGTACTTA[C/T]TGATACTGTATCTGC | 25831 |
rs116866543 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179062 | GGTGAAAAAAAGAAC[A/G]GCAACTGTGTGACTT | 25831 |
rs116868565 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195812 | CAGGCATGAGCCACC[A/G]GTGGAGCCTGGCCTC | 25831 |
rs116893682 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124343 | TCACAGATTTGACCA[C/T]ATCATAGAATAAAAT | 25831 |
rs116898196 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141072 | AGCTGGGATTAAAGA[C/T]GCCCACCACCAGGCC | 25831 |
rs116904831 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120541 | TCGCAACCTCCTATG[A/C]ACCTATAATTATTTT | 25831 |
rs116911303 | snp | A/G | 0.00366724 | 0.0426634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173809 | CTCCATCTGAAACCT[A/G]ACAATGTGAAGAAAA | 25831 |
rs116941066 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209023 | CTATCCGCGCATGTC[C/T]CGTTGTCGCAGGTAA | 25831 |
rs116943446 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115542 | GGTGGACGGATCACT[G/T]GAGCTCAGAAGTTCG | 25831 |
rs116943775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187455 | TCTTATACATCTACA[A/T]AAGAGCTATGTCCAG | 25831 |
rs116950070 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203533 | AGCTACTGAAGAGGC[C/T]GAGGCAGGAGAATCG | 25831 |
rs116982573 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134721 | AGTCAGTGTTTCAAA[C/G]TTTTAATGCCTAAAG | 25831 |
rs116986704 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176586 | TAAAGCAGCAAAAAT[C/T]ATAAAAAGAATGAAG | 25831 |
rs116998112 | snp | G/T | 0.00291168 | 0.0380442 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174873 | ACTAAAAAAATCACT[G/T]TCTGAAAATGGAAAG | 25831 |
rs117003744 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207976 | CTTTTCTATGGTGCG[C/T]CCTGGCCCCCTTTTC | 25831 |
rs117006532 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190425 | TCAGGATGAACTCAC[C/T]GAGTCCAGATTGTGT | 25831 |
rs117010036 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122393 | CATGTGTGTGTGTGT[G/T]TGTGTGTCATTCTGT | 25831 |
rs117012175 | snp | A/G | 0.0103295 | 0.0711199 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099751 | AAACCAGAAAACAGC[A/G]GTATCCCCGTGTTTT | 25831 |
rs117014336 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142961 | ACGTTTCAGCAGTAC[A/G]TATACCAAAACTGAA | 25831 |
rs117014884 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147838 | TTTCTCTGGTCAAAG[C/G]CATAAAAACACAAGA | 25831 |
rs117020837 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157617 | ATAATTTTAGAAAAT[C/T]AAGTAAAAAGTACTA | 25831 |
rs117068255 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110426 | ATCTTAGGCAAATCA[A/G]CTAAGTACGTGCAGA | 25831 |
rs117076615 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108448 | GCAACAGGAAGAGTA[C/T]GGACAAAAACCCTTA | 25831 |
rs117078994 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194175 | ATGATTCCATTTACA[C/T]GACATTCTAGAAAAG | 25831 |
rs117105285 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122709 | TCATGTGACATTCTA[A/T]AATTTTTCAAATATA | 25831 |
rs117108349 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209618 | AACTTAAAAATTTCC[A/G]TCCAGGCTCCATGGC | 25831 |
rs117125419 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123977 | AAACATTGTAATGCT[C/T]TGAAATCGGAATGTA | 25831 |
rs117146878 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151857 | TATAGACAAGATATA[C/T]GAAAAATGTGTTTTC | 25831 |
rs117148971 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178629 | CAACATGGCGAAACC[C/T]CATCTGTACTAAAAA | 25831 |
rs117160106 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139584 | AGAACTGACTCATAA[C/T]TGTAGAATAAGAGGA | 25831 |
rs117186416 | snp | C/T | 0.0107246 | 0.0724382 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100226 | CAAAGAAAATACAAC[C/T]GAAAGTAAAACTCGC | 25831 |
rs117190787 | snp | C/T | 0.00288127 | 0.0378462 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105582 | TATATTAAAAGCAAA[C/T]TTTTTACCTCATCTT | 25831 |
rs117235818 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191489 | GCCAAGATGACACCA[C/T]TGCACTCCAGCCTGG | 25831 |
rs117239620 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171657 | TGAGTGTATAAGAAA[A/G]GGAGGGAACACATAT | 25831 |
rs117241393 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125420 | TCAGGCAATCTGCCC[A/G]CTTCAGCCTCTCAAA | 25831 |
rs117246056 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143569 | TCATCTGTATTTGTT[A/G]TAACTTTAAGCAGAA | 25831 |
rs117260450 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127295 | TAATTTTTTAATAGT[A/C]TCTCGTATTACTGAG | 25831 |
rs117265256 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142013 | GATCTTACTGAAATT[C/T]ATCAAAAACTAAGAG | 25831 |
rs117279326 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126558 | ACACTTCTTCTCTTA[A/G]TGATAAGAGTGTCAA | 25831 |
rs117285675 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175552 | TCCTGGGCAAGAGAG[G/T]GAGACTCTGTCTCAA | 25831 |
rs117296931 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146157 | AGTCAGATTATTCAA[C/T]GGTTCCATGCTTGCA | 25831 |
rs117349822 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159892 | AGATCCACCCTACTC[A/G]GCCTCCCGAAGTGCT | 25831 |
rs117356422 | snp | C/T | 0.00295311 | 0.0383123 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107737 | AAATTGTGGGTTAAA[C/T]GTAAAGTTTGGGGTG | 25831 |
rs117357399 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167929 | CATCCTTACTAGCCC[A/G]CAAGGGGAAGAGTAA | 25831 |
rs117359713 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122479 | CACTAAGTTCATACA[C/T]GTGTGTACGTGTGTG | 25831 |
rs117363532 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120739 | TTGACAGCTCTGGTT[C/T]CAGAATGTTTGGGTT | 25831 |
rs117372919 | snp | A/C | 0.0558544 | 0.157504 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160185 | ATTATCTCAAATTTA[A/C]AAGTGAAGATACTGA | 25831 |
rs117380032 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111008 | GGGACTATCTTCAAA[C/G]TAGTACAAATATTTC | 25831 |
rs117433762 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198940 | ACTCAGGAGGCTAAG[G/T]CGGGAGAACTGCTTG | 25831 |
rs117434603 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141087 | CGCCCACCACCAGGC[C/T]CAACTAACTTTTGTA | 25831 |
rs117461721 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190922 | CTCCCAAAGTGCTGC[A/G]ATTACAGACATGCCC | 25831 |
rs117465690 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152465 | AAAGTGCTGGAGTTA[C/T]AGGCATGAGCCAAGG | 25831 |
rs117468582 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105776 | GTACAAGAGAAAAAA[C/T]TAAATAAAATAACAT | 25831 |
rs117470210 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194838 | GTAATATTTTCTGTA[C/T]TATAACTACCATATG | 25831 |
rs117478352 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123445 | ATGCCTATTTACTAC[A/G]GAATAATGTATGTGG | 25831 |
rs117528040 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204722 | CTTACATACTCAAAA[C/T]TCTGCCAATGACAAA | 25831 |
rs117535326 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117477 | TATCACACTGAATAA[C/T]TGCATCATGAGGTAA | 25831 |
rs117540310 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192479 | AATGAAGCCAAAAGC[G/T]GGTTCTTGGAAAAGG | 25831 |
rs117540521 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181409 | TGCTTGAGTCCAGGA[C/G]TTCAAGAACAGCCTG | 25831 |
rs117542477 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142235 | CAAGATGGTTTCAGA[C/T]TATATTAATATAGGA | 25831 |
rs117556409 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134242 | TGCCAAAAGCAATTT[A/G]GGTACATAATCTACC | 25831 |
rs117559634 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176120 | CATCTGTATGGCAAG[C/G]TAAAGAACTACAAGT | 25831 |
rs117574118 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184276 | CAAGATAGGGAGACC[C/T]GTCTCTAAAAAAAAG | 25831 |
rs117621171 | snp | C/T | 0.00295222 | 0.0383066 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140001 | ACTGCTGGTCGACTG[C/T]GAAGAAATAATTATT | 25831 |
rs117642424 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202243 | CCATGTACAATACTA[A/C]GTTAAAGGAAAAAGA | 25831 |
rs117684740 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166528 | AGGGTTCAAACTAGG[A/C]AGTCGTGTGATATAA | 25831 |
rs117685399 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206651 | TTAAAAAAGGAAAGG[C/T]TAAAAGTAAATGCAA | 25831 |
rs117741858 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168174 | CCACTTCTCATCTAA[A/T]TTTTATTCTTACCAC | 25831 |
rs117759685 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154917 | CTGGGAACCACTAGA[C/G]ACAGAAAAGGTATAT | 25831 |
rs117766257 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174147 | TTTGTCATGATAATC[C/T]ATGATATCAACTGAA | 25831 |
rs117767563 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189529 | AGCACTTTGGGAGGC[C/T]AAGGTGGGATTGCTT | 25831 |
rs117771158 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191144 | CGCCTGGCCTCATTT[C/T]TCCATATACTTAAAC | 25831 |
rs117774788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136450 | CCATAACTCTGGATA[C/T]ATACTTCCCAAATTA | 25831 |
rs117823924 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182913 | TATTATGAATACATT[A/C]ATTGCCAATGCAAAA | 25831 |
rs117830147 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159900 | CCTACTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 25831 |
rs117830856 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140482 | ACAAGGGAAGCTGAG[A/G]AAAGAGAATTGCTTG | 25831 |
rs117833270 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168652 | CTAGTAACTTCAATG[C/T]GCTCAATAACAAATT | 25831 |
rs117839362 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192014 | AACTCCATCTCAAAA[A/G]AAAGAAAGAAAGAAA | 25831 |
rs117839803 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177137 | CCTAAACTTCAAGTC[C/T]TGACTCTTCTGCTCA | 25831 |
rs117846831 | snp | C/T | 0.0032738 | 0.040326 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178137 | CCTTCGGGTACATTC[C/T]GCAGATACATCCAGG | 25831 |
rs117847509 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102757 | TCTTTTTGTATCCTC[A/C]CAGCCTTATCAGTGG | 25831 |
rs117872068 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184879 | CATTGGGAAGAAAAT[A/G]CCAACATTAATTACT | 25831 |
rs117872857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106142 | CATTTATCAAACACA[G/T]TTTACCAACATTATC | 25831 |
rs117904699 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166964 | AATCCCTTGAGGCTA[A/G]GAGTTCAAGACCAGC | 25831 |
rs117919067 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138613 | GTCTGAAACAAAACA[C/T]AAAGTAGCCCTCCAC | 25831 |
rs117948775 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115968 | AACAGAAAGAAGATA[G/T]TTAGTACTCATACAC | 25831 |
rs117982782 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143769 | TTGTTCACACATTAT[A/G]CATATAACTTGGGTA | 25831 |
rs118019227 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153475 | AGCCTCCCCAAAGTG[C/T]TGGGATTACAGGCAT | 25831 |
rs118048408 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201955 | GAAGAAGTTATATTC[C/G]TTGAACTTCAGAAAG | 25831 |
rs118048799 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135673 | TGTTTTCAAGCACGT[G/T]ACCTACTTTTTTCCT | 25831 |
rs118058668 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147739 | CAGTTTGGGCATCAA[C/G]AGCGAAACCGAGTCT | 25831 |
rs118074831 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164299 | TCTGATAAAACTTCA[A/G]AAAAACTGGTAAAAT | 25831 |
rs118081036 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191610 | CAAACTTTGTAGGAT[A/G]CAACTAAAGTAGTAT | 25831 |
rs118085132 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101390 | AAATCACTACCACTA[C/T]TTTCTAAGGCAGCAA | 25831 |
rs118120629 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108272 | ATTCTGTATTTTCAG[C/T]AGAGACAGGGTTTTA | 25831 |
rs118121779 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121283 | GCTCCCTCCTCTCAC[C/T]CCTTCCACACTGCAC | 25831 |
rs118149112 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145943 | TGAGCATAGTACCCA[A/G]CAGTTCTGGAACCCT | 25831 |
rs118180991 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200373 | TTTCTTGGCCAGGCA[C/T]GGTGGCTCACGCCTG | 25831 |
rs118185311 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151767 | AACTTTTTTTGGACA[C/T]ATTTAAAAATGGAAA | 25831 |
rs137873320 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187964 | TTTCACCATGTTGGC[C/T]AGGCTGGTCTCAAAC | 25831 |
rs137928027 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127465 | CAAGCAATTCTTCTG[C/T]CTCAGCCTCCTGAGT | 25831 |
rs137947468 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125469 | TGAGCCACAGCGCCC[A/G]GCCAGTTCACTCTTT | 25831 |
rs137954004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194491 | ATATATAATTACAGT[C/T]GCTCAAAATTTTAAG | 25831 |
rs137970782 | in-del | -/AATGTGTAG | 0.00916344 | 0.0670653 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150225 | TGGTTCATCTTCCTA[-/AATGTGTAG]AATTATTCAATTAAA | 25831 |
rs137980408 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159312 | TTGGTTCTTTCCAGT[C/T]TTTGTTTTGTTGTTT | 25831 |
rs137994781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171124 | TCTTCTACAAACAGA[A/G]TATTTGGCTGGGTGC | 25831 |
rs138013447 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209265 | GATATGTTCCTAGAC[A/T]TAGGAAAGGTCACCT | 25831 |
rs138064483 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137449 | AAACATTCTTTAGGC[C/T]AGGCACAGTGACTCA | 25831 |
rs138095814 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103271 | GAATGGGCTGGGCAC[A/G]GTGGCTCACGCCTGT | 25831 |
rs138147278 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147284 | GCACCGCTGCACTCC[A/T]GTCTGGGTGACAGAG | 25831 |
rs138195265 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133926 | TTTATGATTAATATA[A/C]TTCAAAGATAAAAGA | 25831 |
rs138248344 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148554 | GGTATAAAAATTATA[C/T]GTAAATAAATATTTA | 25831 |
rs138309890 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183768 | GCTAAAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 25831 |
rs138322648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161088 | ATCAATTTGTAAATA[A/C]CCTTTGTATATAATA | 25831 |
rs138343685 | in-del | -/TAAT | 0.0298908 | 0.118541 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143056 | AAATTTTTAAAAATA[-/TAAT]TAATTAATTAATTAA | 25831 |
rs138345584 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108636 | TGAGACCAGCCTGGG[A/C]AACATAGTGAGAACT | 25831 |
rs138348012 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179949 | GGGAGGCTGAGGCAG[A/G]TGGATCACCTGAGGT | 25831 |
rs138389483 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174591 | TCTTATTTAAATGAG[A/C]TCTATCTTAAGTCAA | 25831 |
rs138446389 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189955 | CACTGTGTGACTTCA[A/C]ATGCTAACTCAATGA | 25831 |
rs138450031 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190706 | TTTTATTTTTTGTAG[A/G]GATGGGGGTCTCACT | 25831 |
rs138481157 | snp | G/T | 0.00114134 | 0.0238614 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133254 | ATTGTGTAGTTCTCC[G/T]GTGACAGTGCCTTCT | 25831 |
rs138503664 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123967 | TACATTTTTAAAACA[C/T]TGTAATGCTTTGAAA | 25831 |
rs138534292 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118047 | TCTCACTCTGTCACC[C/T]AGGCTGGAGTGCAGT | 25831 |
rs138537443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187625 | GATCAAATAAATATA[C/T]GAAGGATAATGGGAA | 25831 |
rs138543943 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202874 | GGCAGGTGGATCAGG[A/C]GATCAAGAGATGGAG | 25831 |
rs138586205 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166447 | GCTGGGTTGGGATTA[C/T]GTAAGAACTTGCAAG | 25831 |
rs138608477 | snp | A/G | 0.0310518 | 0.120672 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163161 | CACACGGTGGCTCAC[A/G]CCTGTAAACCCAACA | 25831 |
rs138661854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138713 | GGGAGTCTAGTGGCA[A/C]TGATAACAGTATTGG | 25831 |
rs138768709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112205 | CTAGAAAACATCTAT[C/G]GGGTATCTCTCCTCC | 25831 |
rs138785567 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175720 | AAATATCAAATTAGC[C/T]GGGCATGGTGGCGCA | 25831 |
rs138788107 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108185 | CAACCTCTGCCTCCC[A/G]GGTTCAGGCGATTTT | 25831 |
rs138860077 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113701 | AAGTCTGCATTCAGA[C/T]CCAATGCTACCAGCC | 25831 |
rs138860856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148120 | ACTCTAACTATGAGA[C/T]TATCTTACTTTTTTT | 25831 |
rs138873172 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184532 | GGCAGAGGTTGCAGT[C/G]AGCCAAGATCACGCC | 25831 |
rs138873505 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102734 | CGCGCCCGGCCTGCT[A/G]TCAGTTGTCTTTTTG | 25831 |
rs138925266 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172269 | ATATTTAGGTCAACT[A/G]TAGAGCAGTACATAA | 25831 |
rs138937120 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123480 | TTTCATGTTATCCAT[A/G]TTATCTAGCACATAA | 25831 |
rs138963088 | snp | G/T | 0.029116 | 0.117091 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209760 | TTTAAAATTAGCTGG[G/T]TGTGGTGGTGCACAC | 25831 |
rs138995731 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118195 | ATTTTTAAGTAGAGA[C/T]GGGATTTCACCATGT | 25831 |
rs139132264 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149647 | GTGGCTCACACCTGT[A/G]ACTCCAGCACGTTGG | 25831 |
rs139197958 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157842 | CTCAGGAGCCTGAGG[A/C]GGAATAATCACTTGA | 25831 |
rs139199359 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163527 | AAAATCCCTTGAGCC[C/T]AGGAGTTTGAAGTTG | 25831 |
rs139209811 | in-del | -/AAAAAAAAAGAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161571 | GCAACACCCCGTCTC[-/AAAAAAAAAGAA]AAAAAAAAAGAAAAA | 25831 |
rs139219732 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200338 | TCATCCTTCCTAGCT[A/C]TAGGAAAAACCACTT | 25831 |
rs139260832 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121578 | CTTTCAGCCATGACC[C/T]GAATATATTAACCCC | 25831 |
rs139275158 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192067 | GTGTGGTGGCTCACG[C/T]GTGTAATCCCAGCAC | 25831 |
rs139322188 | snp | C/G | 0.00106097 | 0.0230078 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134904 | GCAGTCATCAACATG[C/G]GTATACAAAGAAGTC | 25831 |
rs139327449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205668 | AAACACAAAACTCTT[C/G]AGGAATATTTTTAAA | 25831 |
rs139421319 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145731 | TTTGATGCATACTTG[C/T]TTATATATGCAAAAG | 25831 |
rs139427895 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140903 | TTAGCAATTAGCTAC[C/T]AATGGCCAATCTCCA | 25831 |
rs139447527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182063 | ATGCCCGGCTAATTT[C/T]TGTATTTTTAGTAGA | 25831 |
rs139461301 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185287 | AAGCTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 25831 |
rs139551915 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115579 | GCATGGGCAACATGG[C/T]AAAAACCCCATCCCT | 25831 |
rs139555804 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185923 | CAGGAAATTTGACCT[C/T]GCTATAAATTTACGA | 25831 |
rs139570026 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194840 | AATATTTTCTGTATT[A/G]TAACTACCATATGCT | 25831 |
rs139600137 | snp | A/G | 0.21875 | 0.248039 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182413 | GCCCAGGCTGGTCTC[A/G]AACTCCTGAGCTCAA | 25831 |
rs139616716 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125789 | GAAAATGGGCTATAC[A/G]CAAAATAGCACCTTA | 25831 |
rs139657867 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103464 | GGAGAATGGCGTGAA[C/T]CCAGGAGGCGGAGCT | 25831 |
rs139661915 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176807 | CCGCGCATGGTGGCA[C/T]GCGCCTGTAGTCCCA | 25831 |
rs139702795 | snp | A/G | 0.030665 | 0.119967 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174563 | AAAAAAATAATAAAA[A/G]TAAAAAATACCGTCT | 25831 |
rs139757384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101706 | CTAAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 25831 |
rs139797658 | snp | A/G | 0.000281487 | 0.0118602 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129186 | ACCCAAGCTGATGTC[A/G]CTGCTACTGGCCACG | 25831 |
rs139811642 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172968 | GTTTTACCCATTCAA[C/T]AAGCATTTATTCAGG | 25831 |
rs139831454 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172369 | AGCACTCTGGGAGGC[C/G]GAGGTGGGAGGAGGT | 25831 |
rs139835446 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125896 | ATCAAGGATATATGG[C/T]AAAGGGTATTCCAAA | 25831 |
rs139862327 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120877 | TTAGTTAATATACAT[A/G]AAGTATTAAGAACTA | 25831 |
rs139898834 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159603 | CCTCAGCCTCCAAAG[C/T]GCTGGGATTACAGGC | 25831 |
rs139919606 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155970 | ATGGAGTCTCAGGCC[A/G]GGTGCGGTGGCTCAC | 25831 |
rs140013629 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104622 | ATCATGATTCTTTCA[C/T]GTTAATTCATCCTGA | 25831 |
rs140023996 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177029 | GCACTAATGCTTTTA[A/G]AGTTACATAAAGACA | 25831 |
rs140051218 | in-del | -/T | 0.0221141 | 0.102801 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167896 | TACCATTTACCACTC[-/T]TATGTTTTACCCACA | 25831 |
rs140073327 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103399 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGCT | 25831 |
rs140092501 | snp | C/T | 0.00349045 | 0.0416298 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101130 | TCTTTCTTTCAAAAG[C/T]AAAGTAACTAAATTT | 25831 |
rs140111732 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140622 | ATCTATAACCTATAA[C/T]ACAGTATTACCACTT | 25831 |
rs140133239 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206414 | TTAGATTCAGTATTT[C/T]GAGGAAACTCTAAAC | 25831 |
rs140146317 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188142 | AGATAGATAGATAGA[C/T]AGACAGACAGATAAA | 25831 |
rs140180097 | snp | C/T | 0.000149267 | 0.00863779 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136698 | AAATACTCTGGAAAA[C/T]GTCTTGGTTTCTGTC | 25831 |
rs140212666 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114761 | AGATATGACTGTATC[A/C]AGTGTTATGCAGCAT | 25831 |
rs140219067 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127347 | GATTCTGTATTTGTT[C/T]GTTGTTTTCTGTTTT | 25831 |
rs140230951 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111460 | GGTTTCACCACGTTA[A/G]CCAGGATGGTCTCGA | 25831 |
rs140240646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170408 | TGCACTCCAGCCTGT[A/G]AGACAGAGCAATACC | 25831 |
rs140247169 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208886 | TGCCACCTCACTCCA[A/G]CCTGGGCGACTAAGC | 25831 |
rs140253483 | snp | C/T | 0.031825 | 0.122064 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110956 | AACTTTTTAAATGCT[C/T]TTTTTTTTTTGGTAA | 25831 |
rs140293500 | in-del | -/TAGT | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115966 | AGAACAGAAAGAAGA[-/TAGT]TAGTACTCATACACG | 25831 |
rs140400005 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149320 | GTACGCATCTGTAGT[C/T]CCAGCTACTTGGGAA | 25831 |
rs140415564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142607 | ACGCCTGGCTAATTT[C/T]GTTTTGTATTTTTAA | 25831 |
rs140444447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116610 | AGACTCTCTAGGCGT[C/T]GACATTTTTGCTTTC | 25831 |
rs140446219 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163079 | CACACACACACACAC[A/G]CACACACACACACAC | 25831 |
rs140450313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186879 | AATACAAAAATCAGC[C/T]GGACGTGGTGGCACA | 25831 |
rs140484179 | snp | C/T | 0.000101014 | 0.00710612 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112578 | AATGTCTTAGTGCTA[C/T]AAGGCATTCATGCAT | 25831 |
rs140488335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182723 | CAGCATGGTGGTGTG[C/T]GCCTGTAGTCCCAGC | 25831 |
rs140550873 | snp | G/T | 0.030665 | 0.119967 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126995 | TTTTTTTTTTGAGAC[G/T]GAGTCTTGCTTTGTC | 25831 |
rs140556710 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196712 | TGAGCCGAGATTGCG[A/C]CACTGCACTCCAGCC | 25831 |
rs140559325 | in-del | -/TAAC | 0.00575792 | 0.0533461 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133195 | TTAAAAGAAAAAATT[-/TAAC]TACCCATTTTCTACA | 25831 |
rs140614957 | in-del | -/GTGTGTGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134562 | TGTGTGTGTGTGTGT[-/GTGTGTGC]GCGCGTATGTATATA | 25831 |
rs140640000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167596 | AACCCTTTGGTAGTT[G/T]GGATCAGAGTACTGA | 25831 |
rs140679149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164538 | ATGCTACACACATAT[C/T]TAATTTTTATTCTCA | 25831 |
rs140717332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200554 | GGAGGCCAAGGCGGG[A/C]GGATCACTTGAGGTC | 25831 |
rs140718123 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132578 | AACAAACCCACTGCC[A/G]TTTAGGCAAATTATC | 25831 |
rs140742236 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169909 | TACAAAGCAGCCTAT[C/G]GTAACTTGAAAAACT | 25831 |
rs140775801 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166004 | CCAAGTGCTACCATA[C/T]CCAGCTAATTTTTTT | 25831 |
rs140780011 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208273 | CCCTTCAGAGCAACC[C/G]TGGGAAAGAGGTGCT | 25831 |
rs140801051 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175662 | TGAGGTCAGGAGTCC[A/G]AGACCAGCCTGACCA | 25831 |
rs140815040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201893 | TTACTTTCTGGAGCA[C/T]TACCTTGATAAGTTC | 25831 |
rs140859364 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196218 | GGGGTTTCTTCGCCA[C/T]GTTGGCCAGGTTGGA | 25831 |
rs140905171 | snp | A/G | 0.0014495 | 0.0268822 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107540 | GCAGAGTCACAACTC[A/G]AGTCACAAAATGAGA | 25831 |
rs140908844 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178681 | GGTGACAGGCACCTG[C/T]AGTCCCAGCTACTCA | 25831 |
rs140916885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119371 | GACTGTAACCACTGG[A/T]TAGCCTTTCAAAACT | 25831 |
rs140938339 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160267 | CTGTATTCAAATTCT[A/G]TCTCTTAATTAGATG | 25831 |
rs141047597 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165903 | TAGGCTGGAATGCAG[C/T]GGCGCAATCTTGGCT | 25831 |
rs141052092 | snp | A/G | 0.000314916 | 0.0125443 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148816 | GGGGGGAAAAAAAAG[A/G]ATATTCACAGAGCTT | 25831 |
rs141103322 | in-del | -/AG | 0.0225045 | 0.103662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188717 | TACAGCACACAGCAG[-/AG]TTTCCTGCACAGAAG | 25831 |
rs141122740 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201535 | TTTTTTTGGAGGCAC[A/G]GTCTCACTCTGTCAC | 25831 |
rs141155102 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149898 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAAATAAA | 25831 |
rs141161645 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194291 | ATGATGTTTCAAAGT[C/G]ATGGAAATGTTCTGC | 25831 |
rs141170089 | in-del | -/AG | 0.0551013 | 0.156571 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156725 | ATTTAAAAAATATAC[-/AG]AATTATTTCATATTG | 25831 |
rs141195309 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147586 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 25831 |
rs141196970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188887 | TACACAACTTCATCC[C/T]GGCCCAATTCCCACA | 25831 |
rs141232383 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186972 | AGGTTGCAGTGAGCC[A/G]AGATCGCACTACTGC | 25831 |
rs141267529 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128468 | ATTCTAGAGAACTTC[A/G]TATTCCTGAACTGCT | 25831 |
rs141269181 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137410 | GCTGGGATTACAGGC[A/G]TGAGACACCACGCCC | 25831 |
rs141271533 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200052 | ACCCAAACTCATGAT[A/C]TCAATCTCTCAAACA | 25831 |
rs141308048 | snp | A/C/T | 4.96827e-05 | 0.0049839 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178113 | TATAGCTCCATCTAC[A/C/T]CCAACAATCCTTCGG | 25831 |
rs141348102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175826 | CCGAGATCGCGCCAC[C/T]GCACTCCAGCCTGGG | 25831 |
rs141424465 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134743 | TGCCTAAAGTATCAA[C/G]TGATTTGTTTTTAGA | 25831 |
rs141444485 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176427 | TTATTTTAAGATAAA[C/T]AAATACTTTAAATTT | 25831 |
rs141463460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132373 | ACCTGGGAAGCAGAG[A/G]TTGCAGTGAGCTGAT | 25831 |
rs141492442 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148253 | ATTATGCATCTGCTA[C/T]TGTATCTTCTTGAAG | 25831 |
rs141511935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187314 | AGTGAGCCAAGATCA[C/T]GCCACTGCATTTCAG | 25831 |
rs141538622 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124838 | TTTGAGATGGAGTCT[C/T]GCTCTGTCACCCAGG | 25831 |
rs141547806 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122498 | TGTACGTGTGTGTGT[A/G]TTTGTGTCATTCTGT | 25831 |
rs141553341 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181270 | GAATAATAGTTCCTG[C/T]TGTGTTCCCTAAAAT | 25831 |
rs141618762 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120656 | ATTACTATGAGGCAG[A/G]CAGCATGTAAGTACA | 25831 |
rs141685296 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31120963 | GTTCAAGAACAGCCT[A/G]GGCAATGAAGCGAAA | 25831 |
rs141688306 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165437 | TTCTTCTCTCTGCCA[A/G]GGTGTCAAAGTGATC | 25831 |
rs141691127 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166458 | ATTATGTAAGAACTT[A/G]CAAGCCTAAGGGTTA | 25831 |
rs141723739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125556 | ATAATAACAAATCAG[C/T]AGAGAGGGGCACAGG | 25831 |
rs141731320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163315 | AGGCATGGTGGCATG[A/C]ATCTGTAGTCTCAGC | 25831 |
rs141762253 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158098 | TGCAACTATGGACTC[A/G]TATAAATGAAAATAA | 25831 |
rs141786497 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166896 | TCTCAGGACAGGTGC[-/A]ATGCAGAAGCTCACA | 25831 |
rs141797622 | in-del | -/CT | 0.0524604 | 0.153226 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200150 | GACACTTCCTTCTCC[-/CT]CTCTCATATTTAATC | 25831 |
rs141844654 | snp | C/G | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099749 | CAAAACCAGAAAACA[C/G]CGGTATCCCCGTGTT | 25831 |
rs141935625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152301 | AAATCACAAATTTGG[C/G]ATCATAGGGGTGAAG | 25831 |
rs141968676 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108193 | GCCTCCCGGGTTCAG[A/G]CGATTTTCCTGCCTC | 25831 |
rs142058682 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105911 | AATCTACTAGGCCAA[A/C]TGTTATCAAATCTGT | 25831 |
rs142089437 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103459 | AGGCAGGAGAATGGC[A/G]TGAATCCAGGAGGCG | 25831 |
rs142089879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149330 | GTAGTCCCAGCTACT[C/T]GGGAAGCTAAGGCGA | 25831 |
rs142098701 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102719 | ACAGGTGTGAGCCAC[C/T]GCGCCCGGCCTGCTG | 25831 |
rs142126134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145076 | TTGGGCACAAATGAG[C/T]TCTCGAAGTTACAGT | 25831 |
rs142186269 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209479 | TCTATCTAGACGAGA[C/T]TAGCTGGAGGTTGTC | 25831 |
rs142264577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122403 | TGTGTGTGTGTGTCA[A/T]TCTGTGGCTCAGGTT | 25831 |
rs142269842 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192698 | GACATTCTACTGGCC[A/G]AGCGTGGTGGTTCAT | 25831 |
rs142366393 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161854 | CCAGCCTGTGCAACA[C/G]AGCAGGACTCTGTCT | 25831 |
rs142406181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199312 | AAATGTAAATTAATG[C/T]CTCTATTCTCCCAAA | 25831 |
rs142406249 | snp | G/T | 0.0611083 | 0.163768 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159403 | GGAGTGCAGTGGTGT[G/T]ATCTCGGCTCACTGC | 25831 |
rs142417688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169795 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 25831 |
rs142472665 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126278 | GGTAGGTGGGGACTA[C/G]ATGATTTTAATTTTC | 25831 |
rs142481183 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110400 | CTCATGTGTGCTACT[A/G]TTTTCTCATGATCTT | 25831 |
rs142510768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123374 | TCAATCAGTGAAAAA[C/T]GGGGCTTAGATATGT | 25831 |
rs142517260 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193403 | TCTATTTCTGAACTC[C/T]ATATTCTGTTCCACA | 25831 |
rs142525906 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175465 | CAGCTACTCAGGAGG[C/T]TGAGGTGAGAGGATC | 25831 |
rs142539389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114962 | CTAAACATAAAAAAG[A/G]TACAGTAAAAATGTG | 25831 |
rs142551252 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194522 | CTTGCCAAGTATTTA[A/C]CTCTTACATTACAGG | 25831 |
rs142555656 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190267 | TACCCTTTCCAGTTT[C/T]CAAAATCCAGATAAT | 25831 |
rs142582456 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161580 | CGTCTCAAAAAAAAA[A/G]AAAAAAAAAAAGAAA | 25831 |
rs142611374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155289 | GGTGGAGGGGGCGGT[G/T]AGCCGAGATCATGCC | 25831 |
rs142630762 | in-del | -/AA | 0.0123036 | 0.0774623 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120830 | ATTAGGGCTAACAAT[-/AA]AACCCTAAAAAGGTT | 25831 |
rs142691531 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185069 | TGCTTCTGGCCGGGC[A/G]CGGTGGCTCACGCCT | 25831 |
rs142779653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143711 | TCTTTGGAAAACAAG[C/T]CCTGTGGAGAGTTCC | 25831 |
rs142805982 | snp | C/T | 0.00172846 | 0.029347 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102906 | GATCTTGGAAAATAG[C/T]ATCACATACCTGTCA | 25831 |
rs142819559 | in-del | -/A | 0.0456336 | 0.143994 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184583 | GCCACACCCTGTCTC[-/A]AAAAAAAAATTAGCT | 25831 |
rs142825938 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195928 | GTAAACCCTCACAGA[C/G]AGTGTTTCTCATTCC | 25831 |
rs142843136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172332 | TTTAAGTCCAGGCAC[C/T]GTGGCTCACGCCTGT | 25831 |
rs142901720 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140073 | AAAATATGGTAATCA[A/T]CTTCAATATATACCC | 25831 |
rs142901874 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184186 | ATGCACAGTAGCTCA[C/T]TGCTGTAATCCTAGC | 25831 |
rs142932945 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103557 | CAAAAAAAAAAAAGA[A/G]TGAAATCTTTTCATT | 25831 |
rs142940973 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200978 | ACATAAGGTGCTGTA[C/T]TTGTTTTGGTCATCA | 25831 |
rs142942694 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180078 | AGCTACTCAGGAGGC[A/T]AAGGCAGGAGAATTG | 25831 |
rs142949453 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145621 | GGCTGCAGTGAGCCA[A/T]GATTGTGCCAGTGCC | 25831 |
rs142988766 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209834 | TGAGCCCTCGAGGTC[A/G]AAGCTGCAGTGAGCC | 25831 |
rs143024068 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123889 | AGGCCTGCCATTATA[G/T]TTCATTAGTTTCTAA | 25831 |
rs143028503 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204212 | AATAAACATACGTGT[G/T]CATGTGTCTTTATAG | 25831 |
rs143041513 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137102 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC | 25831 |
rs143147642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142308 | TATTAGGAAAAAACT[A/G]GTACATCAAAACTAT | 25831 |
rs143150425 | snp | A/G | 0.00110379 | 0.0234665 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171975 | CTGTAAAATGATAAC[A/G]AATCATAAAGCTGCT | 25831 |
rs143181641 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117745 | AAACGGGGTACAGAG[C/T]TAATATTTAAAATTA | 25831 |
rs143205242 | snp | A/G/T | 0.00319074 | 0.0398324 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208366 | CCCAGCGCCGTGCCC[A/G/T]GTCGGCAGCAGCACT | 25831 |
rs143219781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114510 | TGTAGAGATAAGGTT[C/T]TGCTATGTTGTCCAG | 25831 |
rs143268004 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117368 | CAGAACGAGACTCCA[C/T]CTCAAAAAAAAATTT | 25831 |
rs143275097 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187074 | AAAAACAGGCCTGGC[A/G]TGGTGGCTCACGCCT | 25831 |
rs143350653 | in-del | -/A | 0.00117677 | 0.0242281 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148824 | AAAAAGAATATTCAC[-/A]AGAGCTTACTTTGTT | 25831 |