SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs763441075 | snp | A/T | 1.81929e-05 | 0.00301598 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009946 | GCCTTGAGGGGTGTG[A/T]CTATATCTTGCCTGG | 79654 |
rs763508117 | snp | C/T | 3.91934e-05 | 0.00442664 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012845 | GGCCTTATGAACCCG[C/T]GCTTTCCCCAGCCTC | 79654 |
rs763525446 | snp | A/G | 1.66067e-05 | 0.00288151 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45006069 | GGCAAAGTCTCGGCA[A/G]GAGGGGTTGGGTACA | 79654 |
rs763531505 | snp | A/G | 1.66774e-05 | 0.00288763 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010336 | GGGGAGACATCAGCG[A/G]TCAGCAAGACACTAC | 79654 |
rs763590298 | snp | C/T | 0.000398466 | 0.0141094 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010278 | TGAGTATGTCAGGTC[C/T]ACCACCTGTTCCCAC | 79654 |
rs763628232 | snp | C/T | 4.52745e-05 | 0.00475765 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012837 | ACTGAATCGGCCTTA[C/T]GAACCCGCGCTTTCC | 79654 |
rs763798033 | snp | C/G | 1.67158e-05 | 0.00289096 | missense | HECTD3 | GRCh38.p7 | 1:45003924 | ACAAAGCGCAGGAAG[C/G]GGCTCCGGTCCTCTG | 79654 |
rs763879013 | snp | C/T | 1.65644e-05 | 0.00287783 | missense | HECTD3 | GRCh38.p7 | 1:45007447 | TTGCAGGCAGGGTCT[C/T]GAGAGGGGCAGGCAC | 79654 |
rs763932802 | snp | A/G | 1.66687e-05 | 0.00288688 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009363 | TCCCCAGGCCAGCGT[A/G]CTCACTCGTCAATGC | 79654 |
rs764003054 | snp | A/G | 5.45777e-05 | 0.00522359 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012099 | AGGTAGGGGTCCTAC[A/G]GGCAGCAGCCAGGGC | 79654 |
rs764054588 | in-del | -/CC | 1.65633e-05 | 0.00287774 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003632 | CAGGGGTGATGGGGT[-/CC]CCTGGGCCCCAAATC | 79654 |
rs764067548 | snp | A/G | 0.000252048 | 0.0112232 | upstream-variant-2KB, synonymous-codon | UROD, HECTD3 | GRCh38.p7 | 1:45011078 | CACCGGCAGAAGCAC[A/G]CGCGACGGTCCCGCT | 79654 |
rs764154031 | snp | C/T | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003089 | CTCCAGTGTTTTATG[C/T]TTTTAGTTGTGAGTC | 79654 |
rs764196954 | snp | A/G | 3.63908e-05 | 0.00426545 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009970 | TGCCTGGGGTGGGAG[A/G]AGCCCCAGCACCCAC | 79654 |
rs764268015 | snp | A/G | 1.65509e-05 | 0.00287666 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012960 | TGCGAGCAGCCTGGG[A/G]AGAGGAAACAGACTA | 79654 |
rs764291434 | snp | C/T | 1.65616e-05 | 0.00287759 | splice-acceptor-variant | HECTD3 | GRCh38.p7 | 1:45003578 | CGCATACCTTGGCAC[C/T]GTGGGAATGGGGACT | 79654 |
rs764350114 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45006392 | CTCACTGCAACCTCC[A/G]TCTCCTGGGTTCAAG | 79654 |
rs764363669 | snp | A/C | 1.67399e-05 | 0.00289304 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45006794 | GTCCCGGAAACCACC[A/C]CCTGAAATGACAGAT | 79654 |
rs764374191 | snp | C/G | 1.68023e-05 | 0.00289843 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010675 | CAGCCTTCCTGCAGC[C/G]CGCAGTCGCCCAGGT | 79654 |
rs764378114 | snp | C/T | 1.66327e-05 | 0.00288376 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004184 | CTCATCTTGCCCAGT[C/T]CTTGAGCCCCAACCC | 79654 |
rs764390100 | snp | A/C | 1.66424e-05 | 0.0028846 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009523 | GTCTTTGTGAACCCA[A/C]AGGGACATAGCCCAC | 79654 |
rs764426557 | snp | A/G | 1.69263e-05 | 0.0029091 | missense | HECTD3 | GRCh38.p7 | 1:45006699 | GAGATTACCTGGTTG[A/G]CTGTGCGTACAAAGA | 79654 |
rs764462041 | snp | C/G | 1.6896e-05 | 0.0029065 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010756 | GGAACTGCCCAGCCG[C/G]CTGTCGTGCCCAGCC | 79654 |
rs764462775 | snp | C/G | 1.65732e-05 | 0.00287859 | missense | HECTD3 | GRCh38.p7 | 1:45008677 | TTGATCTTGACCCCT[C/G]GGAGACGAACATCAA | 79654 |
rs764703581 | snp | A/C | 1.66123e-05 | 0.00288199 | missense | HECTD3 | GRCh38.p7 | 1:45009580 | TACTTGACAATGGTG[A/C]CCTTCTTCATAGTAA | 79654 |
rs764785541 | snp | A/G | 1.76499e-05 | 0.00297063 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010559 | ACCTGAGCACCGGCC[A/G]ATAATCCACGCCAAA | 79654 |
rs764843175 | snp | A/C | 3.31241e-05 | 0.00406952 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45007461 | TCGAGAGGGGCAGGC[A/C]CGGTGTTCCATGGCA | 79654 |
rs764867617 | snp | C/T | 1.65916e-05 | 0.00288019 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45009398 | GTCACTCAGCTTCTT[C/T]AGGTTGTCCCCTTCA | 79654 |
rs764933323 | snp | C/T | 8.27917e-05 | 0.00643343 | missense | HECTD3 | GRCh38.p7 | 1:45004661 | AAACGAGAACGGTCC[C/T]CATATCCCACGACGA | 79654 |
rs764948790 | snp | C/T | 4.50116e-05 | 0.00474381 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012114 | GGGCAGCAGCCAGGG[C/T]AGCCCTGGAGCTGTC | 79654 |
rs764970660 | snp | C/T | 3.31285e-05 | 0.00406978 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45007446 | CTTGCAGGCAGGGTC[C/T]CGAGAGGGGCAGGCA | 79654 |
rs765004956 | in-del | -/TGTT | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45007165 | GTGTGTGTTTGTGTG[-/TGTT]TGTGTGCACAAACAG | 79654 |
rs765027418 | snp | C/T | 1.65641e-05 | 0.00287781 | missense | HECTD3 | GRCh38.p7 | 1:45003518 | AAGGGCTCATGTCAG[C/T]GTCGATGGCCACGCA | 79654 |
rs765041628 | snp | A/T | 3.62286e-05 | 0.00425594 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012174 | TGGCGACGCTCTTGG[A/T]TCCCTACAGAAAGGG | 79654 |
rs765055863 | in-del | -/CT | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45009081 | TTCTCTCCACACACA[-/CT]CTCTGTTTGCCCCCA | 79654 |
rs765075487 | snp | C/T | 1.66751e-05 | 0.00288744 | missense | HECTD3 | GRCh38.p7 | 1:45007567 | AGGCCTGGCCGCTGG[C/T]GGGACAGCAGTAGGA | 79654 |
rs765117087 | snp | A/G | 1.65619e-05 | 0.00287762 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003601 | TGGGGACTTGGTCAG[A/G]TCCCTACATCGCTAC | 79654 |
rs765189134 | snp | A/G | 8.28068e-05 | 0.00643402 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013061 | ATAAAACTCCGGAGG[A/G]AGAAAAGTTTTCGAG | 79654 |
rs765214024 | snp | A/G | 0.000116041 | 0.00761624 | missense | HECTD3 | GRCh38.p7 | 1:45008684 | TGACCCCTCGGAGAC[A/G]AACATCAATCCCATC | 79654 |
rs765302869 | snp | A/G | 3.31203e-05 | 0.00406928 | missense | HECTD3 | GRCh38.p7 | 1:45008597 | CTTCTAGGCGTGGAT[A/G]TCGCACCAGACTAGT | 79654 |
rs765323499 | in-del | -/C | 1.66007e-05 | 0.00288098 | frameshift-variant | HECTD3 | GRCh38.p7 | 1:45008248 | GGCTCACCTTAATCT[-/C]ACTGAAGGTGCCCAG | 79654 |
rs765354435 | snp | A/C | | | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45010980 | AGCTCAATGCTGTCG[A/C]GGGCGGCGCGGAGGG | 79654 |
rs765374955 | in-del | -/T | 1.66785e-05 | 0.00288773 | frameshift-variant | HECTD3 | GRCh38.p7 | 1:45004071 | TGACCGTTGGTGAAG[-/T]TGTTCAGTGCCTCCC | 79654 |
rs765460280 | snp | G/T | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45005683 | CCATGGGAGTGGATG[G/T]ATTGGAGAGGGATCT | 79654 |
rs765465970 | snp | A/C | 1.97303e-05 | 0.00314082 | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45010935 | TTGCACAGCTCCTCG[A/C]CCGTGGTGCGCACGC | 79654 |
rs765472159 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45013188 | CACGTGTCGCTCTCC[C/T]GAGGCCTGCTGTGAA | 79654 |
rs765505591 | snp | C/T | 1.66432e-05 | 0.00288467 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004205 | GCCCCAACCCCTGTG[C/T]TGTGCTGTGCTGCCC | 79654 |
rs765524441 | snp | A/G | 4.97715e-05 | 0.00498831 | missense, utr-variant-5-prime | HECTD3 | GRCh38.p7 | 1:45009599 | TCTTCATAGTAAGCC[A/G]TACCCAGTGTTGGCA | 79654 |
rs765549861 | snp | A/G | 1.6799e-05 | 0.00289814 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008199 | AACTACGTGAGCAGG[A/G]AGGGGAAATGCCAAG | 79654 |
rs765819779 | snp | A/G | 1.65641e-05 | 0.00287781 | missense | HECTD3 | GRCh38.p7 | 1:45008293 | CAGGTACCAGGTGGT[A/G]CAGGACACTATCGAG | 79654 |
rs765898694 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012274 | GCTGACCATGGAAGC[A/G]AATGGGTTGGGGTGA | 79654 |
rs765923606 | snp | A/C | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45005556 | TGAGCCTGAGATGCC[A/C]TCTTGGGGCAAACGT | 79654 |
rs765931158 | snp | C/T | 1.66344e-05 | 0.0028839 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009515 | GAATATGAGTCTTTG[C/T]GAACCCACAGGGACA | 79654 |
rs765995134 | snp | A/G | 3.85097e-05 | 0.00438786 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012124 | CAGGGCAGCCCTGGA[A/G]CTGTCGCTGGAGTCC | 79654 |
rs765999782 | snp | A/G | 1.65605e-05 | 0.0028775 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45004798 | TTCCATCACTTCCAG[A/G]AGCTTCACCTAGGGG | 79654 |
rs766020219 | snp | C/T | 1.68097e-05 | 0.00289906 | missense | HECTD3 | GRCh38.p7 | 1:45007585 | GACAGCAGTAGGAAC[C/T]GCTTCACTTGCTAGT | 79654 |
rs766050622 | snp | C/T | 0.000132488 | 0.00813795 | missense | HECTD3 | GRCh38.p7 | 1:45004368 | GCAGACCTGCCTGCA[C/T]AGCTGCCACCTGGGG | 79654 |
rs766087994 | snp | A/G | 1.65622e-05 | 0.00287764 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003612 | TCAGGTCCCTACATC[A/G]CTACCAGGGGTGATG | 79654 |
rs766089147 | snp | C/T | 1.76918e-05 | 0.00297415 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012178 | GACGCTCTTGGTTCC[C/T]TACAGAAAGGGGCGG | 79654 |
rs766103537 | snp | C/T | 1.65751e-05 | 0.00287876 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010170 | CCAGACGCAGAGCTC[C/T]TTCCTCCCCACCCCA | 79654 |
rs766184633 | snp | A/G | 8.42439e-05 | 0.00648959 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008190 | GGAATGAACAACTAC[A/G]TGAGCAGGAAGGGGA | 79654 |
rs766193815 | snp | C/T | 1.65902e-05 | 0.00288008 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010258 | GGTCTCGATCCCAGG[C/T]GATGTGAGTATGTCA | 79654 |
rs766195663 | snp | C/T | 3.62825e-05 | 0.0042591 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005762 | CCTTTAGGGGCTGGG[C/T]AGAGGAAACACTGGT | 79654 |
rs766276038 | snp | C/T | 6.65425e-05 | 0.00576774 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009116 | CCACGCCGGGCTCTC[C/T]TTCCCTCCTTATAGC | 79654 |
rs766362274 | snp | G/T | 0.000157421 | 0.0088705 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007168 | TGTGTTTGTGTGTGT[G/T]TGTGTGCACAAACAG | 79654 |
rs766422451 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45009815 | GGTATGGGATAGGGG[A/G]CCGCTGGGTATGTAA | 79654 |
rs766429386 | snp | C/T | 4.96857e-05 | 0.00498401 | missense | HECTD3 | GRCh38.p7 | 1:45008647 | TTCAACCCTAGTTCC[C/T]GCTGTCTAGATGACT | 79654 |
rs766486124 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45013205 | AGGCCTGCTGTGAAC[G/T]GACTCTGCAGGTGAG | 79654 |
rs766500529 | snp | A/C/T | 3.29512e-05 | 0.00405891 | missense, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45013350 | ACATCCTTGTTGTAC[A/C/T]CCAGGTACCCACTCA | 79654 |
rs766504102 | snp | C/T | 4.10762e-05 | 0.00453171 | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45010957 | TGCGCACGCAGGCGC[C/T]GCGCCGGAGCTCAAT | 79654 |
rs766573377 | snp | C/G | | | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012812 | TGGAGGAGGTAGATA[C/G]CGGTCCTGGACTGAA | 79654 |
rs766576380 | snp | C/G | 1.656e-05 | 0.00287745 | missense | HECTD3 | GRCh38.p7 | 1:45004334 | AGCAAGTCCAGCACA[C/G]CCTGTGGTACCACCT | 79654 |
rs766638625 | snp | A/G | 3.63841e-05 | 0.00426506 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009949 | TTGAGGGGTGTGACT[A/G]TATCTTGCCTGGGGT | 79654 |
rs766640645 | in-del | -/TTCCACACACTCT | 1.65653e-05 | 0.00287792 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008333 | AATCTGGCATGGGTA[-/TTCCACACACTCT]GATAGACTGCAGCTA | 79654 |
rs766662130 | snp | C/T | 3.31549e-05 | 0.0040714 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004427 | AGGGCACACCTCCCG[C/T]CTCACACTGGGGGGC | 79654 |
rs766689406 | snp | C/T | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45006847 | GCCCAGCTCCCATAA[C/T]GGGGTAATGAATAGG | 79654 |
rs766715692 | snp | C/G | 1.65644e-05 | 0.00287783 | missense | HECTD3 | GRCh38.p7 | 1:45008315 | ACTATCGAGGATCTT[C/G]ATGAATCTGGCATGG | 79654 |
rs766732259 | snp | A/C | 1.67758e-05 | 0.00289614 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008420 | GGCAGGACCTGGGGG[A/C]TTCTCTGACCCTTGA | 79654 |
rs766819824 | snp | G/T | 9.97722e-05 | 0.0070623 | missense | HECTD3 | GRCh38.p7 | 1:45006076 | TCTCGGCAGGAGGGG[G/T]TGGGTACATACATGT | 79654 |
rs766874559 | snp | C/T | 4.99879e-05 | 0.00499915 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004023 | AACTCAGCAGCAGAG[C/T]CCAAACCCAGGTGTC | 79654 |
rs766980312 | snp | C/T | 1.66128e-05 | 0.00288204 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012934 | TCCGGAGCTGAAGAA[C/T]GACACATTCCTGCGA | 79654 |
rs767012968 | snp | A/G | 1.66435e-05 | 0.0028847 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012199 | AAAGGGGCGGAGCCT[A/G]GACTGGGGGGCAGGC | 79654 |
rs767043881 | snp | C/G | 1.68374e-05 | 0.00290145 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008194 | TGAACAACTACGTGA[C/G]CAGGAAGGGGAAATG | 79654 |
rs767054601 | snp | A/C | 1.64779e-05 | 0.00287031 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012263 | AGTTACAGACAGCTG[A/C]CCATGGAAGCGAATG | 79654 |
rs767117244 | snp | A/G | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003146 | TAGGAGAAAAAAGGC[A/G]GAGCTGAAAATGGAG | 79654 |
rs767140463 | snp | G/T | 1.65941e-05 | 0.00288041 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010263 | CGATCCCAGGCGATG[G/T]GAGTATGTCAGGTCC | 79654 |
rs767231247 | snp | A/G | 3.34163e-05 | 0.00408742 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005961 | CCTTCCAAGGGCCAG[A/G]GCTGATCGGACGGGG | 79654 |
rs767231301 | snp | C/T | 1.65633e-05 | 0.00287774 | missense | HECTD3 | GRCh38.p7 | 1:45003736 | GCGCGTCTGTGGTCT[C/T]GTAGCTGGGGGCATT | 79654 |
rs767282913 | snp | A/G | 1.6669e-05 | 0.00288691 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010333 | GATGGGGAGACATCA[A/G]CGGTCAGCAAGACAC | 79654 |
rs767332812 | snp | C/T | 1.69493e-05 | 0.00291108 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007177 | GTGTGTTTGTGTGCA[C/T]AAACAGGTGTCCCGA | 79654 |
rs767390717 | snp | A/T | 1.66518e-05 | 0.00288542 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003810 | GTGTGGGGAGGGAGG[A/T]CAGAAGGCGGCCATG | 79654 |
rs767438575 | snp | A/C/T | 3.42596e-05 | 0.0041387 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009701 | GGGGAGGGGCAGAGA[A/C/T]GTGAAGTCAGCAGTT | 79654 |
rs767491813 | snp | C/G | 1.65734e-05 | 0.00287862 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004558 | GGAGCTGGGGCTCAG[C/G]AGGGGCCAAAGCTCT | 79654 |
rs767496484 | snp | A/G | 5.01333e-05 | 0.00500641 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007278 | TTCATATACCTGGAG[A/G]CAAGGAGGAAAGGAG | 79654 |
rs767510163 | snp | A/G | 1.6708e-05 | 0.00289028 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003441 | CTTCGCCCTGGGCAA[A/G]GCCAAGAGGGACACG | 79654 |
rs767638082 | snp | C/T | 0.000356952 | 0.0133547 | upstream-variant-2KB, synonymous-codon | UROD, HECTD3 | GRCh38.p7 | 1:45011051 | ACGCAGCCCCAGGCC[C/T]TCTGCCTCCCACACC | 79654 |
rs767648849 | snp | C/G | 1.65597e-05 | 0.00287743 | missense | HECTD3 | GRCh38.p7 | 1:45004641 | CCTTCTGGACCAGTT[C/G]GATGAAACGAGAACG | 79654 |
rs767710379 | snp | A/C | 1.6582e-05 | 0.00287936 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012947 | AATGACACATTCCTG[A/C]GAGCAGCCTGGGGAG | 79654 |
rs767740586 | snp | C/T | 1.658e-05 | 0.00287919 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003488 | CCACAGCCGGCGGCA[C/T]GCCTCACTCCTCCCA | 79654 |
rs767761514 | snp | A/C | 1.65677e-05 | 0.00287812 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45008571 | GCGGTACAGTACTTC[A/C]GGGTCGGTGCCTTCT | 79654 |
rs767782047 | snp | A/G | 1.74766e-05 | 0.00295601 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006661 | TCAATCTGGCACCTG[A/G]GAGGTTTGCAGAGAT | 79654 |
rs767796386 | snp | C/T | 3.57347e-05 | 0.00422683 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010582 | ACGCCAAAGAGCTGC[C/T]GCTGCCGCTGGAGGT | 79654 |
rs767858608 | snp | A/G | 1.66219e-05 | 0.00288283 | missense | HECTD3 | GRCh38.p7 | 1:45006082 | CAGGAGGGGTTGGGT[A/G]CATACATGTCCCGAG | 79654 |
rs767897686 | snp | A/G | 0.000248746 | 0.0111495 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010719 | CTCCTGCCGGGACGC[A/G]TAGGATGGGGACAGC | 79654 |
rs768045578 | snp | A/G | 6.61813e-05 | 0.00575207 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013037 | AAGAGTCAGGGTCTG[A/G]AAATCTAGATAAAAC | 79654 |
rs768082262 | in-del | -/TA | 1.81936e-05 | 0.00301603 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009948 | CTTGAGGGGTGTGAC[-/TA]TATCTTGCCTGGGGT | 79654 |
rs768148953 | snp | C/G | 1.81946e-05 | 0.00301611 | missense, intron-variant | HECTD3 | GRCh38.p7 | 1:45010003 | TGTAGGAGGAAACGT[C/G]TATGCTCTCCACATA | 79654 |
rs768178276 | snp | A/C | 1.65809e-05 | 0.00287926 | missense | HECTD3 | GRCh38.p7 | 1:45009418 | TGTCCCCTTCACCCC[A/C]ATAGACCACCACCCG | 79654 |
rs768306928 | snp | C/T | 3.37735e-05 | 0.00410921 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012908 | CACCTGATCGCCAGA[C/T]CTCAGGGTTTTCCGG | 79654 |
rs768311442 | snp | C/G | 5.05199e-05 | 0.00502568 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006145 | AGAGCTGTGAGTGTG[C/G]CATGAGATACACCCT | 79654 |
rs768326253 | snp | C/T | 1.9792e-05 | 0.00314573 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010617 | GGGAGTGTCGATGGG[C/T]ACCAGGCGGGCTCCG | 79654 |
rs768398049 | snp | C/T | 1.66721e-05 | 0.00288717 | missense | HECTD3 | GRCh38.p7 | 1:45004131 | TCGAAGTCCTCAAAC[C/T]GGGCTGGTGGAGACA | 79654 |
rs768451707 | in-del | -/A | 1.99667e-05 | 0.00315958 | intron-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012877 | GCGTAGCATACTGAC[-/A]ACCTACCCCCACCCC | 79654 |
rs768466340 | snp | C/T | 1.65277e-05 | 0.00287464 | stop-gained, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012998 | GTTTGGTGCATGCGC[C/T]AGGCAGGCCGTTACT | 79654 |
rs768473119 | snp | A/G | 1.66788e-05 | 0.00288775 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45004061 | CCTCCTCCACTGACC[A/G]TTGGTGAAGTTGTTC | 79654 |
rs768527804 | snp | C/G | 1.65888e-05 | 0.00287996 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45007536 | GCTCTCAGAGTCACG[C/G]AGGCACTGAGCCACC | 79654 |
rs768691179 | snp | C/T | 3.31186e-05 | 0.00406918 | missense | HECTD3 | GRCh38.p7 | 1:45004749 | ATGTTAGTTCCTTCC[C/T]AAACTTGAACTCAAA | 79654 |
rs768777282 | snp | C/T | 1.81602e-05 | 0.00301326 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005744 | AGCCTTAGGGAGGAC[C/T]AACCTTTAGGGGCTG | 79654 |
rs768834569 | snp | C/T | | | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013080 | AAAGTTTTCGAGGGG[C/T]AGGGGAGGGCTCTGG | 79654 |
rs768892933 | snp | A/G | 0.000117563 | 0.00766601 | intron-variant | HECTD3 | GRCh38.p7 | 1:45010124 | CGGGGGTACATAGCT[A/G]AGCAACCCCAAGCCC | 79654 |
rs768938405 | snp | C/G | 1.64741e-05 | 0.00286998 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45013176 | GGACTTTTTCAGCAC[C/G]TGTCGCTCTCCTGAG | 79654 |
rs769000775 | snp | A/G | 1.66969e-05 | 0.00288932 | missense | HECTD3 | GRCh38.p7 | 1:45007231 | TACCTGTAGTCCAGG[A/G]GCTTTTCATATTTGT | 79654 |
rs769129547 | snp | A/G | 1.65296e-05 | 0.00287481 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013022 | CGTTACTTACCAGGT[A/G]AGAGTCAGGGTCTGG | 79654 |
rs769152793 | snp | A/G | 1.65751e-05 | 0.00287876 | missense | HECTD3 | GRCh38.p7 | 1:45009162 | GGCACTCCACGATGC[A/G]GATCTCGATGATCGG | 79654 |
rs769166045 | snp | A/C | 8.27972e-05 | 0.00643364 | missense | HECTD3 | GRCh38.p7 | 1:45004297 | ATCCCCACACACTTT[A/C]TTCTCCAACTCTTGC | 79654 |
rs769167391 | snp | A/G | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002673 | TAGGAACAGGTTTAA[A/G]GTCTAGGCTTTAGAG | 79654 |
rs769187842 | snp | A/G | 1.95984e-05 | 0.00313031 | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45010915 | TCACCCAGAGCCCGT[A/G]GCCATTGCACAGCTC | 79654 |
rs769231957 | snp | C/T | 4.98998e-05 | 0.00499474 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008237 | CTGGCTGGGTCGGCT[C/T]ACCTTAATCTCACTG | 79654 |
rs769274003 | snp | A/G | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002822 | GAATATGGGGAGGTC[A/G]TGGTAGTAGAGTTCA | 79654 |
rs769291990 | snp | C/T | 1.65608e-05 | 0.00287752 | missense | HECTD3 | GRCh38.p7 | 1:45008630 | GCTGGAACAGGTCTG[C/T]ATTCAACCCTAGTTC | 79654 |
rs769292057 | snp | C/T | 1.69223e-05 | 0.00290876 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006157 | GTGGCATGAGATACA[C/T]CCTATTTTCCTGGCC | 79654 |
rs769378741 | snp | A/T | 1.64806e-05 | 0.00287054 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45013140 | TCTGTATGCAGAGTT[A/T]AGGGAAACCCGGGCT | 79654 |
rs769452119 | snp | C/G | 1.66613e-05 | 0.00288623 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004148 | GGCTGGTGGAGACAA[C/G]GCCAGCATTCATTCT | 79654 |
rs769456782 | snp | A/C/T | 9.94026e-05 | 0.00704929 | missense | HECTD3 | GRCh38.p7 | 1:45004256 | AACTCACTGAGCTTG[A/C/T]GCAGAGCATCCACAG | 79654 |
rs769575577 | snp | C/T | 1.81516e-05 | 0.00301255 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005751 | GGGAGGACCAACCTT[C/T]AGGGGCTGGGCAGAG | 79654 |
rs769621027 | snp | A/G | 1.70232e-05 | 0.00291741 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010733 | CGTAGGATGGGGACA[A/G]CCGTCAGGGAACTGC | 79654 |
rs769716249 | snp | C/G | 1.65828e-05 | 0.00287943 | missense, utr-variant-5-prime | HECTD3 | GRCh38.p7 | 1:45009628 | CACTGGGACCCATCG[C/G]TCTCCCAGTAGGTAT | 79654 |
rs769766810 | snp | C/T | 3.29647e-05 | 0.00405971 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012243 | AAATTGTGGATTGAG[C/T]TCGCAGTTACAGACA | 79654 |
rs769768604 | snp | A/G | 0.000249516 | 0.0111667 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010311 | GTGGGCACAGAGTAG[A/G]GAGTGGGATGGGGAG | 79654 |
rs769797282 | snp | C/G | | | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011650 | CCTCCCACTCCCAGC[C/G]AATCTGCTGGACTCC | 79654 |
rs769822423 | snp | C/T | | | missense | HECTD3 | GRCh38.p7 | 1:45006052 | CCGATCCATTCATAC[C/T]TGGCAAAGTCTCGGC | 79654 |
rs769842621 | in-del | -/CT | 1.64741e-05 | 0.00286998 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45013182 | TTTCAGCACGTGTCG[-/CT]CTCCTGAGGCCTGCT | 79654 |
rs769850849 | snp | A/G | 1.64784e-05 | 0.00287035 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012299 | GGGTGAGTTCTCCAG[A/G]GCACGCGGTGTGGCT | 79654 |
rs769858136 | snp | C/T | 1.65732e-05 | 0.00287859 | missense | HECTD3 | GRCh38.p7 | 1:45009186 | TGATCGGGAGGTGGA[C/T]GGTCATGTCCTCCAG | 79654 |
rs769888577 | snp | A/C | 1.73417e-05 | 0.00294458 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005915 | CCCCACTGTCTTCTC[A/C]CCCTGAGCTGCCCAG | 79654 |
rs769906600 | snp | C/G | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003059 | CTCCCTGCTTGGGGA[C/G]GGGCCTCCACTAACC | 79654 |
rs769906721 | snp | C/T | 3.31702e-05 | 0.00407235 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010248 | TGCCGGCTGAGGTCT[C/T]GATCCCAGGCGATGT | 79654 |
rs769922443 | snp | C/G | 1.65721e-05 | 0.0028785 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003780 | TCAGGAAGATGTGTT[C/G]GGGCACATGTACGTG | 79654 |
rs769981297 | snp | C/T | 4.94214e-05 | 0.00497074 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, missense | UROD, HECTD3 | GRCh38.p7 | 1:45013333 | TGCCATCATTTTCTC[C/T]GACATCCTTGTTGTA | 79654 |
rs770221134 | snp | C/T | 1.66244e-05 | 0.00288304 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003472 | TGCAGTCTTGCTGGT[C/T]CCACAGCCGGCGGCA | 79654 |
rs770250908 | snp | A/T | 1.66735e-05 | 0.00288729 | missense | HECTD3 | GRCh38.p7 | 1:45007250 | TTTCATATTTGTCAG[A/T]GGGCTTGAGGCCTTC | 79654 |
rs770254053 | snp | C/T | 2.90213e-05 | 0.00380917 | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45011206 | AGAAGCGCACGCGGC[C/T]CAGCAGCTGCCGGGG | 79654 |
rs770310674 | snp | C/T | | | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012646 | GGGCCTTCATTCCCT[C/T]CCCCCAGTCCCTCTG | 79654 |
rs770338516 | snp | C/T | 1.65726e-05 | 0.00287855 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004418 | CTGGGGAAGAGGGCA[C/T]ACCTCCCGCCTCACA | 79654 |
rs770338592 | snp | C/T | 0.00010016 | 0.00707602 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007376 | CCCCTTGGCCCTTGA[C/T]TGATCCTATCTCAGT | 79654 |
rs770355077 | snp | C/T | 1.65608e-05 | 0.00287752 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45004618 | CTCCTTGCTCTCCTC[C/T]AGCCGTGCCTTCTGG | 79654 |
rs770369883 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013277 | ACCTAGCAACCTGTC[C/T]CCTGTTTCCTACAGC | 79654 |
rs770398564 | snp | G/T | 1.66441e-05 | 0.00288474 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004175 | TTCTTGGGTCTCATC[G/T]TGCCCAGTCCTTGAG | 79654 |
rs770441245 | in-del | -/TGTGTG | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45007129 | TGCCTCGAGCAGTTG[-/TGTGTG]TGTGTGTGTGTGTGT | 79654 |
rs770486371 | snp | A/T | 1.65625e-05 | 0.00287766 | missense | HECTD3 | GRCh38.p7 | 1:45004265 | AGCTTGCGCAGAGCA[A/T]CCACAGTGACCTCTG | 79654 |
rs770502811 | snp | A/G | 1.6563e-05 | 0.00287771 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004380 | GCATAGCTGCCACCT[A/G]GGGAGTGGGTAAAAA | 79654 |
rs770503931 | snp | C/T | 1.96771e-05 | 0.00313658 | upstream-variant-2KB, synonymous-codon | UROD, HECTD3 | GRCh38.p7 | 1:45010901 | CACCTTTGTCAGCTT[C/T]ACCCAGAGCCCGTGG | 79654 |
rs770596403 | snp | A/G/T | 3.32398e-05 | 0.00407664 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45009570 | AGAGCCTACTTACTT[A/G/T]ACAATGGTGCCCTTC | 79654 |
rs770656150 | snp | C/T | 1.64779e-05 | 0.00287031 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012257 | GCTCGCAGTTACAGA[C/T]AGCTGACCATGGAAG | 79654 |
rs770669046 | snp | C/T | 3.31735e-05 | 0.00407255 | missense, utr-variant-5-prime | HECTD3 | GRCh38.p7 | 1:45009644 | TCTCCCAGTAGGTAT[C/T]GGCATTGCTGTCTGT | 79654 |
rs770788725 | in-del | -/A | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002977 | TGAGGGCAGGTGCTC[-/A]AGCTACTGCTTCCTT | 79654 |
rs770845741 | snp | A/G | 3.32226e-05 | 0.00407556 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45008243 | GGGTCGGCTCACCTT[A/G]ATCTCACTGAAGGTG | 79654 |
rs770867858 | snp | A/G | 1.72249e-05 | 0.00293465 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005929 | CACCCTGAGCTGCCC[A/G]GGTTTGGCTGGCCTT | 79654 |
rs770895115 | snp | C/T | 1.66402e-05 | 0.00288441 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010315 | GCACAGAGTAGGGAG[C/T]GGGATGGGGAGACAT | 79654 |
rs770922154 | snp | C/T | 1.6729e-05 | 0.00289209 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009345 | GAACATGCCCTACTT[C/T]CCTCCCCAGGCCAGC | 79654 |
rs770941117 | snp | C/T | 1.93714e-05 | 0.00311213 | intron-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012880 | GTAGCATACTGACAC[C/T]TACCCCCACCCCCAC | 79654 |
rs770953716 | snp | C/T | 1.65811e-05 | 0.00287929 | missense | HECTD3 | GRCh38.p7 | 1:45006027 | CCGAAGGGCAGCCCC[C/T]ATCAGCTGTCCGATC | 79654 |
rs770959754 | snp | A/G/T | 3.31252e-05 | 0.00406958 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004593 | TCTACTAGCCTCTGG[A/G/T]TACTACCTGCTCCTT | 79654 |
rs770979037 | snp | A/T | | | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012015 | ATGTCACCGTAAGAT[A/T]CATTTACAGCGGAGT | 79654 |
rs770983281 | snp | C/G | 1.81365e-05 | 0.0030113 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010526 | TCTGACAGCCAGCCC[C/G]GCTCCTTCAAGTGCA | 79654 |
rs771010265 | snp | A/G | 3.33133e-05 | 0.00408112 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007393 | GATCCTATCTCAGTC[A/G]GACCCTAGGTGGTGC | 79654 |
rs771049426 | snp | A/G | 3.33817e-05 | 0.00408531 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45007266 | GGGCTTGAGGCCTTC[A/G]TATACCTGGAGGCAA | 79654 |
rs771099833 | snp | A/G | 0.000175454 | 0.00936463 | upstream-variant-2KB, synonymous-codon | UROD, HECTD3 | GRCh38.p7 | 1:45011012 | CCCGGAGCCGGTACC[A/G]GGGGCTGGGCCTGCG | 79654 |
rs771300669 | snp | C/T | 3.31356e-05 | 0.00407022 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45007500 | GTTGATGTATAGGCG[C/T]GGCATGAAGCTGGGC | 79654 |
rs771331452 | snp | C/T | 0.000200064 | 0.00999959 | missense, intron-variant | HECTD3 | GRCh38.p7 | 1:45010027 | CCACATACTGCTTCA[C/T]GCTACCCAGGTTCTC | 79654 |
rs771372035 | snp | A/G | | | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010732 | GCGTAGGATGGGGAC[A/G]GCCGTCAGGGAACTG | 79654 |
rs771384912 | snp | A/G | 3.31181e-05 | 0.00406914 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45004690 | GATGCCTGCACCCCC[A/G]GGGATCAGCTCCACC | 79654 |
rs771392195 | snp | A/C | 1.7719e-05 | 0.00297644 | missense, intron-variant | HECTD3 | GRCh38.p7 | 1:45010092 | ATCAGGTCCTCGTCG[A/C]ACTCGTAGGTCCATG | 79654 |
rs771395444 | snp | A/C | 1.65597e-05 | 0.00287743 | missense | HECTD3 | GRCh38.p7 | 1:45004626 | TCTCCTCTAGCCGTG[A/C]CTTCTGGACCAGTTG | 79654 |
rs771459941 | snp | C/T | 1.65679e-05 | 0.00287814 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004398 | GAGTGGGTAAAAAGG[C/T]TTGGCTGGGGAAGAG | 79654 |
rs771477805 | snp | A/G | 1.65886e-05 | 0.00287993 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45008543 | ACAGCCACCTCTGCA[A/G]GAGGACAGCTCTGCG | 79654 |
rs771553446 | snp | A/C | 1.8271e-05 | 0.00302244 | upstream-variant-2KB, synonymous-codon | UROD, HECTD3 | GRCh38.p7 | 1:45010997 | GGCGGCGCGGAGGGG[A/C]CCGGAGCCGGTACCG | 79654 |
rs771703610 | snp | C/T | 1.66258e-05 | 0.00288316 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008365 | AGAGTTTAGCATACC[C/T]GTAACACCCCCAACT | 79654 |
rs771729604 | in-del | -/G | 1.67075e-05 | 0.00289023 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007056 | CATTATGTGGGGCCA[-/G]GTGCAGCACAATTCA | 79654 |
rs771791025 | snp | A/G | 3.58173e-05 | 0.00423171 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010537 | GCCCCGCTCCTTCAA[A/G]TGCAGTACCTGAGCA | 79654 |
rs771823923 | snp | C/G | 4.99214e-05 | 0.00499582 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012813 | GGAGGAGGTAGATAG[C/G]GGTCCTGGACTGAAT | 79654 |
rs772048197 | snp | A/C/T | 0.000150203 | 0.0086649 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009360 | CCCTCCCCAGGCCAG[A/C/T]GTGCTCACTCGTCAA | 79654 |
rs772065990 | snp | C/G | 0.000749856 | 0.0193485 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004042 | AACCCAGGTGTCACC[C/G]TGCCCTCCTCCACTG | 79654 |
rs772092015 | snp | A/G | 3.66274e-05 | 0.00427929 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010603 | CGCTGGAGGTGGTTG[A/G]GAGTGTCGATGGGTA | 79654 |
rs772138066 | snp | C/T | 1.65866e-05 | 0.00287976 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45009467 | ATCTGTGGTATCCAC[C/T]GTGAGTAGCAGCTTC | 79654 |
rs772154513 | snp | C/T | 1.65767e-05 | 0.00287891 | missense | HECTD3 | GRCh38.p7 | 1:45007523 | AGCTGGGCTTGCTGC[C/T]CTCAGAGTCACGCAG | 79654 |
rs772411959 | snp | A/G | 6.70028e-05 | 0.00578765 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008744 | TTTACAGCACCTGCT[A/G]CCTCCTTGGCCCTCA | 79654 |
rs772457955 | snp | C/T | 1.65833e-05 | 0.00287948 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004844 | GAGGTAACCTTTTCA[C/T]TGTGGAGATAGTCCC | 79654 |
rs772459573 | snp | A/C | 5.17907e-05 | 0.00508848 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012144 | CGCTGGAGTCCGATC[A/C]TGTGATCTTCAACAT | 79654 |
rs772465310 | snp | A/C | 1.81823e-05 | 0.0030151 | missense, intron-variant | HECTD3 | GRCh38.p7 | 1:45010035 | TGCTTCACGCTACCC[A/C]GGTTCTCATCCTCCT | 79654 |
rs772494067 | snp | A/G | 1.65622e-05 | 0.00287764 | missense | HECTD3 | GRCh38.p7 | 1:45008648 | TCAACCCTAGTTCCC[A/G]CTGTCTAGATGACTT | 79654 |
rs772553433 | snp | A/G | 3.31219e-05 | 0.00406938 | missense | HECTD3 | GRCh38.p7 | 1:45003672 | GAAAAAACCCACCTG[A/G]CATAGTGTGGCAGGA | 79654 |
rs772554745 | snp | A/G | 1.70609e-05 | 0.00292065 | synonymous-codon, intron-variant | HECTD3 | GRCh38.p7 | 1:45010112 | GTAGGTCCATGTCGG[A/G]GGTACATAGCTAAGC | 79654 |
rs772560290 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45005479 | GGAGGAGTGGGACAT[A/G]GTGCCCTTCTGAGGC | 79654 |
rs772561258 | snp | A/G | 5.44055e-05 | 0.00521534 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010596 | CTGCTGCCGCTGGAG[A/G]TGGTTGGGAGTGTCG | 79654 |
rs772574384 | in-del | -/T | | | frameshift-variant | HECTD3 | GRCh38.p7 | 1:45003670 | AGGAAAAAACCCACC[-/T]GGCATAGTGTGGCAG | 79654 |
rs772582103 | snp | A/G | 1.66651e-05 | 0.00288657 | missense | HECTD3 | GRCh38.p7 | 1:45006762 | GGGCACAGCTCTTCT[A/G]ACATATCTGCCAGGC | 79654 |
rs772631777 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45013172 | CCCAGGACTTTTTCA[C/G]CACGTGTCGCTCTCC | 79654 |
rs772645947 | snp | A/G | 1.66565e-05 | 0.00288583 | missense | HECTD3 | GRCh38.p7 | 1:45006738 | GGCACGGGGGTATCC[A/G]CTGAGCTAGGGCACA | 79654 |
rs772646025 | snp | C/T | 1.66846e-05 | 0.00288826 | missense | HECTD3 | GRCh38.p7 | 1:45004099 | CCCAGAAATACTGCA[C/T]CCGCGAGTCAGATGG | 79654 |
rs772664098 | snp | A/G | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002888 | GGTGGCACTTTGTGT[A/G]TTGAGACTGGGTTGG | 79654 |
rs772709645 | snp | A/C | 1.70246e-05 | 0.00291754 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010734 | GTAGGATGGGGACAG[A/C]CGTCAGGGAACTGCC | 79654 |
rs772758699 | in-del | -/AGA | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45005423 | ATATGGTGGCGAGGG[-/AGA]AGAAGGGGTGAAGGA | 79654 |
rs772800200 | snp | C/T | 1.65748e-05 | 0.00287874 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010641 | GGCTCCGCCCTCCGC[C/T]GGGCGGCACACCAGC | 79654 |
rs772896898 | snp | A/C | | | intron-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012887 | ACTGACACCTACCCC[A/C]ACCCCCACCTGATCG | 79654 |
rs772968135 | snp | A/G | 1.66241e-05 | 0.00288302 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009500 | GAAGGGTCAGAGTGT[A/G]AATATGAGTCTTTGT | 79654 |
rs773043308 | snp | G/T | 1.80185e-05 | 0.00300149 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012175 | GGCGACGCTCTTGGT[G/T]CCCTACAGAAAGGGG | 79654 |
rs773056261 | snp | A/G | 1.66244e-05 | 0.00288304 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009562 | TCCTGCCCAGAGCCT[A/G]CTTACTTGACAATGG | 79654 |
rs773093390 | snp | C/T | 1.73387e-05 | 0.00294432 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005917 | CCACTGTCTTCTCAC[C/T]CTGAGCTGCCCAGGT | 79654 |
rs773179837 | snp | A/C | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45006816 | ATGACAGATGCCCTC[A/C]GCTGGGCACTCAAGA | 79654 |
rs773181966 | snp | A/G | 3.63016e-05 | 0.00426022 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005754 | AGGACCAACCTTTAG[A/G]GGCTGGGCAGAGGAA | 79654 |
rs773275798 | in-del | -/CCTGTGCTGT | 1.65655e-05 | 0.00287793 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008325 | TCTTGATGAATCTGG[-/CCTGTGCTGT]CATGGGTAGATAGAC | 79654 |
rs773400923 | in-del | -/CCAACTCAGGACTCTATCCCTCTACTCCCCTTTCCCCACC | 1.64734e-05 | 0.00286992 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45013309 | CTGCGTCGCTTCCCT[lengthTooLong]CTGGATGCTGCCATC | 79654 |
rs773490860 | snp | A/C | 2.00074e-05 | 0.0031628 | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45010944 | TCCTCGCCCGTGGTG[A/C]GCACGCAGGCGCCGC | 79654 |
rs773513980 | snp | A/C | 1.67172e-05 | 0.00289108 | missense, utr-variant-5-prime | HECTD3 | GRCh38.p7 | 1:45009678 | GCAGGACACGTTGAA[A/C]TCCTCCTGGGGAGGG | 79654 |
rs773545209 | snp | C/T | 1.66918e-05 | 0.00288888 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007028 | CACCTGCAAAAAACG[C/T]GGGCAGATTTGTCAT | 79654 |
rs773651311 | snp | C/T | 0.000546815 | 0.016526 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004420 | GGGGAAGAGGGCACA[C/T]CTCCCGCCTCACACT | 79654 |
rs773737357 | snp | C/T | 3.31203e-05 | 0.00406928 | missense | HECTD3 | GRCh38.p7 | 1:45004622 | TTGCTCTCCTCTAGC[C/T]GTGCCTTCTGGACCA | 79654 |
rs773765370 | snp | C/G | 1.81926e-05 | 0.00301595 | missense, intron-variant | HECTD3 | GRCh38.p7 | 1:45010019 | TATGCTCTCCACATA[C/G]TGCTTCACGCTACCC | 79654 |
rs773765514 | snp | A/G | 1.67609e-05 | 0.00289486 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008399 | CAACATAAAGGGACA[A/G]GAAAAGGCAGGACCT | 79654 |
rs773794015 | snp | A/C | 1.656e-05 | 0.00287745 | missense | HECTD3 | GRCh38.p7 | 1:45004288 | GACCTCTGGATCCCC[A/C]CACACTTTCTTCTCC | 79654 |
rs773813792 | snp | A/G | 4.97888e-05 | 0.00498918 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003481 | GCTGGTCCCACAGCC[A/G]GCGGCACGCCTCACT | 79654 |
rs773843770 | snp | C/T | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45009742 | CCTGCACTGGGCTTG[C/T]GCTCTGGGCCAGGAG | 79654 |
rs773846339 | snp | G/T | 1.65875e-05 | 0.00287984 | missense, utr-variant-5-prime | HECTD3 | GRCh38.p7 | 1:45009646 | TCCCAGTAGGTATCG[G/T]CATTGCTGTCTGTCA | 79654 |
rs773905460 | snp | C/T | 1.64779e-05 | 0.00287031 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012260 | CGCAGTTACAGACAG[C/T]TGACCATGGAAGCGA | 79654 |
rs774146690 | snp | A/G | 1.66477e-05 | 0.00288506 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003809 | TGTGTGGGGAGGGAG[A/G]ACAGAAGGCGGCCAT | 79654 |
rs774152839 | snp | C/T | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45005277 | TGCATGGAGACCAAA[C/T]GGGTAAGAACGGAGA | 79654 |
rs774180068 | snp | C/G | 1.65913e-05 | 0.00288017 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010259 | GTCTCGATCCCAGGC[C/G]ATGTGAGTATGTCAG | 79654 |
rs774195718 | snp | A/G | 3.33845e-05 | 0.00408548 | missense | HECTD3 | GRCh38.p7 | 1:45003906 | AGGCGACTGCGGCCC[A/G]TGACAAAGCGCAGGA | 79654 |
rs774203382 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45005326 | AGTAAGTGATTAGCT[A/G]AGGAGGAAAGGTGTC | 79654 |
rs774208873 | snp | A/G | 1.65853e-05 | 0.00287964 | missense | HECTD3 | GRCh38.p7 | 1:45008256 | TTAATCTCACTGAAG[A/G]TGCCCAGTGTGTGGT | 79654 |
rs774219947 | snp | A/G | 1.66443e-05 | 0.00288477 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003808 | GTGTGTGGGGAGGGA[A/G]GACAGAAGGCGGCCA | 79654 |
rs774222736 | snp | C/G | 1.67158e-05 | 0.00289096 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005956 | CCTTTCCTTCCAAGG[C/G]CCAGGGCTGATCGGA | 79654 |
rs774249649 | snp | A/G | 0.000214226 | 0.0103473 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012320 | CGGTGTGGCTAGCCG[A/G]GCTTCTAATTTGAGT | 79654 |
rs774256907 | snp | A/G | 1.67089e-05 | 0.00289035 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007275 | GCCTTCATATACCTG[A/G]AGGCAAGGAGGAAAG | 79654 |
rs774288032 | snp | A/T | 1.65754e-05 | 0.00287879 | missense | HECTD3 | GRCh38.p7 | 1:45009212 | TCCAGGACACAGACA[A/T]CCCCGATGAGGGTCC | 79654 |
rs774311737 | snp | C/T | 1.65814e-05 | 0.00287931 | missense | HECTD3 | GRCh38.p7 | 1:45006038 | CCCCCATCAGCTGTC[C/T]GATCCATTCATACTT | 79654 |
rs774365914 | snp | C/T | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002689 | GTCTAGGCTTTAGAG[C/T]TGGGGAAAGGGGAGC | 79654 |
rs774375997 | snp | C/T | 1.67133e-05 | 0.00289074 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009348 | CATGCCCTACTTCCC[C/T]CCCCAGGCCAGCGTG | 79654 |
rs774418565 | snp | C/T | 1.65789e-05 | 0.0028791 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004428 | GGGCACACCTCCCGC[C/T]TCACACTGGGGGGCA | 79654 |
rs774422835 | snp | A/C | | | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013264 | CCTTCAGTCTGCCAC[A/C]TAGCAACCTGTCTCC | 79654 |
rs774530141 | snp | A/G | 1.81899e-05 | 0.00301573 | synonymous-codon, intron-variant | HECTD3 | GRCh38.p7 | 1:45010028 | CACATACTGCTTCAC[A/G]CTACCCAGGTTCTCA | 79654 |
rs774611008 | snp | G/T | 1.66561e-05 | 0.00288579 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007406 | TCGGACCCTAGGTGG[G/T]GCAGACCTGGGTGAA | 79654 |
rs774646122 | snp | A/C/T | 3.6387e-05 | 0.00426526 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009950 | TGAGGGGTGTGACTA[A/C/T]ATCTTGCCTGGGGTG | 79654 |
rs774707782 | snp | C/T | 3.31923e-05 | 0.0040737 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012941 | CTGAAGAATGACACA[C/T]TCCTGCGAGCAGCCT | 79654 |
rs774712115 | snp | A/G | 1.98833e-05 | 0.00315297 | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45011014 | CGGAGCCGGTACCGG[A/G]GGCTGGGCCTGCGGC | 79654 |
rs774718533 | snp | A/G | 1.68255e-05 | 0.00290043 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012089 | CGGTGAAAAAAGGTA[A/G]GGGTCCTACGGGCAG | 79654 |
rs774800396 | snp | A/G | 3.31735e-05 | 0.00407255 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003484 | GGTCCCACAGCCGGC[A/G]GCACGCCTCACTCCT | 79654 |
rs774871050 | snp | C/T | 3.31483e-05 | 0.004071 | missense | HECTD3 | GRCh38.p7 | 1:45009161 | CGGCACTCCACGATG[C/T]GGATCTCGATGATCG | 79654 |
rs774873843 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45008416 | AAAAGGCAGGACCTG[A/G]GGGCTTCTCTGACCC | 79654 |
rs774899040 | snp | C/T | 5.26977e-05 | 0.00513284 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006650 | CCCTTTCTAGCTCAA[C/T]CTGGCACCTGGGAGG | 79654 |
rs774937597 | snp | A/G | 1.81906e-05 | 0.00301579 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009938 | TGGATCTAGCCTTGA[A/G]GGGTGTGACTATATC | 79654 |
rs774981068 | snp | G/T | 1.65614e-05 | 0.00287757 | missense | HECTD3 | GRCh38.p7 | 1:45008643 | TGCATTCAACCCTAG[G/T]TCCCGCTGTCTAGAT | 79654 |
rs774981559 | snp | G/T | 1.66324e-05 | 0.00288374 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008367 | AGTTTAGCATACCTG[G/T]AACACCCCCAACTCC | 79654 |
rs774987950 | snp | G/T | 5.31505e-05 | 0.00515484 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012821 | TAGATAGCGGTCCTG[G/T]ACTGAATCGGCCTTA | 79654 |
rs775191812 | snp | C/T | | | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45008285 | GTCCCAGGCAGGTAC[C/T]AGGTGGTGCAGGACA | 79654 |
rs775210041 | snp | C/G | 1.74272e-05 | 0.00295183 | intron-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012895 | CTACCCCCACCCCCA[C/G]CTGATCGCCAGACCT | 79654 |
rs775261801 | snp | A/G | 1.67044e-05 | 0.00288997 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005965 | CCAAGGGCCAGGGCT[A/G]ATCGGACGGGGGTGT | 79654 |
rs775302600 | snp | C/T | 0.000125294 | 0.007914 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010538 | CCCCGCTCCTTCAAG[C/T]GCAGTACCTGAGCAC | 79654 |
rs775366617 | snp | A/G | 0.000165585 | 0.00909753 | missense | HECTD3 | GRCh38.p7 | 1:45004647 | GGACCAGTTGGATGA[A/G]ACGAGAACGGTCCCC | 79654 |
rs775366926 | snp | C/G | 1.66985e-05 | 0.00288946 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45003917 | GCCCGTGACAAAGCG[C/G]AGGAAGCGGCTCCGG | 79654 |
rs775383501 | snp | A/G | | | missense | HECTD3 | GRCh38.p7 | 1:45006014 | GGAACTCCTTACCCC[A/G]AAGGGCAGCCCCCAT | 79654 |
rs775400761 | in-del | -/T | 1.68235e-05 | 0.00290026 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007202 | TCCCGAGTAAGTCCC[-/T]CACTCTCATGCCATA | 79654 |
rs775454987 | snp | G/T | 1.6669e-05 | 0.00288691 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004043 | ACCCAGGTGTCACCC[G/T]GCCCTCCTCCACTGA | 79654 |
rs775467472 | snp | C/T | 1.6569e-05 | 0.00287824 | missense | HECTD3 | GRCh38.p7 | 1:45007433 | TGAAGACTGCATTCT[C/T]GCAGGCAGGGTCTCG | 79654 |
rs775510536 | snp | A/G | | | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012748 | GTGCACCACCTGATA[A/G]GCAGAGAGGAGGCGG | 79654 |
rs775557641 | snp | C/T | | | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011709 | TTTGAGACAATGGCC[C/T]CTTCCCCTGCCACTG | 79654 |
rs775660247 | snp | A/G | 1.65594e-05 | 0.0028774 | missense | HECTD3 | GRCh38.p7 | 1:45004739 | ACAGTGGTGAATGTT[A/G]GTTCCTTCCCAAACT | 79654 |
rs775681338 | snp | C/G/T | 9.93801e-05 | 0.00704855 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45008658 | TTCCCGCTGTCTAGA[C/G/T]GACTTGATCTTGACC | 79654 |
rs775759581 | snp | A/C/T | 0.00023013 | 0.0107248 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012093 | GAAAAAAGGTAGGGG[A/C/T]CCTACGGGCAGCAGC | 79654 |
rs775771269 | snp | A/G | | | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012404 | CCCAACCTGAACTCC[A/G]TTAGCTGGGATCCTG | 79654 |
rs775799010 | snp | C/T | 3.3129e-05 | 0.00406982 | missense | HECTD3 | GRCh38.p7 | 1:45008576 | ACAGTACTTCAGGGT[C/T]GGTGCCTTCTAGGCG | 79654 |
rs775821706 | snp | A/G | 3.31235e-05 | 0.00406948 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45003576 | CTCGCATACCTTGGC[A/G]CTGTGGGAATGGGGA | 79654 |
rs775838807 | snp | C/T | 1.67072e-05 | 0.00289021 | missense | HECTD3 | GRCh38.p7 | 1:45006783 | TCTGCCAGGCTGTCC[C/T]GGAAACCACCCCCTG | 79654 |
rs775847498 | snp | C/T | 4.64069e-05 | 0.00481677 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012152 | TCCGATCATGTGATC[C/T]TCAACATGGCGACGC | 79654 |
rs775870394 | snp | G/T | 1.65501e-05 | 0.00287659 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013041 | GTCAGGGTCTGGAAA[G/T]CTAGATAAAACTCCG | 79654 |
rs775962228 | snp | C/T | 4.94222e-05 | 0.00497078 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45013173 | CCAGGACTTTTTCAG[C/T]ACGTGTCGCTCTCCT | 79654 |
rs776024517 | snp | A/C/T | 0.000101011 | 0.00710613 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006148 | GCTGTGAGTGTGGCA[A/C/T]GAGATACACCCTATT | 79654 |
rs776052198 | snp | G/T | 1.65935e-05 | 0.00288036 | missense | HECTD3 | GRCh38.p7 | 1:45008539 | GACCACAGCCACCTC[G/T]GCAGGAGGACAGCTC | 79654 |
rs776132645 | snp | A/C | 1.66638e-05 | 0.00288645 | missense | HECTD3 | GRCh38.p7 | 1:45006991 | AAATTTACACTCCCA[A/C]CACTGGTCATAGCGC | 79654 |
rs776136343 | snp | A/G | 0.00778914 | 0.0619185 | missense | HECTD3 | GRCh38.p7 | 1:45006071 | CAAAGTCTCGGCAGG[A/G]GGGGTTGGGTACATA | 79654 |
rs776183050 | snp | C/T | 3.33622e-05 | 0.00408412 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45004082 | GAAGTTGTTCAGTGC[C/T]TCCCAGAAATACTGC | 79654 |
rs776224338 | snp | A/G | 5.01023e-05 | 0.00500486 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45003932 | CAGGAAGCGGCTCCG[A/G]TCCTCTGGAGGGAGA | 79654 |
rs776332239 | snp | A/C | 3.36853e-05 | 0.00410384 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012911 | CTGATCGCCAGACCT[A/C]AGGGTTTTCCGGAGC | 79654 |
rs776423045 | snp | C/T | 8.82511e-05 | 0.00664212 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010557 | GTACCTGAGCACCGG[C/T]CGATAATCCACGCCA | 79654 |
rs776439380 | snp | A/T | 2.00407e-05 | 0.00316543 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010618 | GGAGTGTCGATGGGT[A/T]CCAGGCGGGCTCCGC | 79654 |
rs776441077 | snp | G/T | 2.12091e-05 | 0.0032564 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012159 | ATGTGATCTTCAACA[G/T]GGCGACGCTCTTGGT | 79654 |
rs776470528 | snp | A/G | 6.66844e-05 | 0.00577389 | missense | HECTD3 | GRCh38.p7 | 1:45004132 | CGAAGTCCTCAAACC[A/G]GGCTGGTGGAGACAA | 79654 |
rs776502697 | in-del | -/G | 1.6825e-05 | 0.00290038 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012913 | GATCGCCAGACCTCA[-/G]GGTTTTCCGGAGCTG | 79654 |
rs776520282 | snp | C/T | 1.66776e-05 | 0.00288765 | intron-variant | HECTD3 | GRCh38.p7 | 1:45010131 | ACATAGCTAAGCAAC[C/T]CCAAGCCCCTAATTA | 79654 |
rs776552550 | in-del | -/A | 1.65688e-05 | 0.00287821 | frameshift-variant | HECTD3 | GRCh38.p7 | 1:45007435 | AGACTGCATTCTTGC[-/A]AGGCAGGGTCTCGAG | 79654 |
rs776604623 | snp | A/C | 3.32038e-05 | 0.00407441 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45007545 | GTCACGCAGGCACTG[A/C]GCCACCAGGCCTGGC | 79654 |
rs776612987 | snp | A/G | 4.99089e-05 | 0.00499519 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012107 | GTCCTACGGGCAGCA[A/G]CCAGGGCAGCCCTGG | 79654 |
rs776632259 | snp | A/G | 3.31235e-05 | 0.00406948 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003579 | GCATACCTTGGCACT[A/G]TGGGAATGGGGACTT | 79654 |
rs776746761 | in-del | -/A | 1.65614e-05 | 0.00287757 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003657 | CAAATCGAGCCTAGG[-/A]AAAAAACCCACCTGG | 79654 |
rs776865777 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45013180 | TTTTTCAGCACGTGT[C/T]GCTCTCCTGAGGCCT | 79654 |
rs776907084 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45013317 | GCTTCCCTCTGGATG[C/G]TGCCATCATTTTCTC | 79654 |
rs776958881 | snp | A/G | 1.65729e-05 | 0.00287857 | stop-gained | HECTD3 | GRCh38.p7 | 1:45008678 | TGATCTTGACCCCTC[A/G]GAGACGAACATCAAT | 79654 |
rs777022635 | in-del | -/TG | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45005118 | AAGGCCTAAGGAAAC[-/TG]TGTGGCTGGAGCCTG | 79654 |
rs777027053 | snp | C/T | 1.97213e-05 | 0.00314011 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010840 | AACAGCCAGAGGTTT[C/T]TCTGGCCCCAGGGGT | 79654 |
rs777068872 | snp | C/G | 1.66782e-05 | 0.0028877 | missense | HECTD3 | GRCh38.p7 | 1:45007010 | TGGTCATAGCGCATG[C/G]GCCACCTGCAAAAAA | 79654 |
rs777076131 | snp | C/G | 1.9618e-05 | 0.00313187 | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45010911 | AGCTTCACCCAGAGC[C/G]CGTGGCCATTGCACA | 79654 |
rs777084732 | snp | C/T | 1.66977e-05 | 0.00288939 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008733 | GAGTAAGGTCATTTA[C/T]AGCACCTGCTGCCTC | 79654 |
rs777139726 | snp | C/T | 0.000133271 | 0.00816197 | missense, utr-variant-5-prime | HECTD3 | GRCh38.p7 | 1:45009671 | CTGTCAGGCAGGACA[C/T]GTTGAACTCCTCCTG | 79654 |
rs777274326 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45004496 | GGAATGGTGGGGGCC[A/G]GAGTTCTTGGAGTAC | 79654 |
rs777286954 | snp | A/T | 0.000648007 | 0.0179884 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006931 | AGCAGGACCCTTGAG[A/T]TCCTCCCTCAGGGCC | 79654 |
rs777367548 | snp | A/G | 1.65963e-05 | 0.0028806 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009137 | TCCTTATAGCCTTAA[A/G]CCTCACCTCGGCACT | 79654 |
rs777389495 | snp | C/T | 2.48543e-05 | 0.00352513 | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45010978 | GGAGCTCAATGCTGT[C/T]GCGGGCGGCGCGGAG | 79654 |
rs777417148 | snp | A/G | 3.31312e-05 | 0.00406995 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003756 | CTGGGGGCATTGAGG[A/G]ACCATAGGTCAGGAA | 79654 |
rs777419225 | in-del | -/CTGCC | 1.66471e-05 | 0.00288501 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004214 | CTGTGCTGTGCTGTG[-/CTGCC]CTGCCCTGCCCTGCC | 79654 |
rs777445736 | snp | A/G/T | 6.74597e-05 | 0.00580741 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007191 | ACAAACAGGTGTCCC[A/G/T]AGTAAGTCCCTCACT | 79654 |
rs777477131 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013272 | CTGCCACCTAGCAAC[C/T]TGTCTCCTGTTTCCT | 79654 |
rs777494863 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45008940 | TCCTCTTCCAGGTGA[A/G]CCCAACCACCTGTAT | 79654 |
rs777495541 | snp | C/G | 1.96953e-05 | 0.00313804 | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45010897 | AGCGCACCTTTGTCA[C/G]CTTCACCCAGAGCCC | 79654 |
rs777548921 | in-del | -/G | 0.000531085 | 0.0162868 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012203 | GGCGGAGCCTGGACT[-/G]GGGGGGCAGGCTCAG | 79654 |
rs777703172 | snp | C/G | 1.64789e-05 | 0.0028704 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012300 | GGTGAGTTCTCCAGA[C/G]CACGCGGTGTGGCTA | 79654 |
rs777716735 | snp | G/T | 1.66751e-05 | 0.00288744 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003451 | GGCAAGGCCAAGAGG[G/T]ACACGTGCAGTCTTG | 79654 |
rs777746576 | snp | C/G | 1.66749e-05 | 0.00288741 | missense | HECTD3 | GRCh38.p7 | 1:45006106 | TCCCGAGCCTCACCA[C/G]TGCCATTGCCCTGCC | 79654 |
rs777780712 | snp | C/G | 0.000114308 | 0.00755916 | intron-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012868 | CCAGCCTCCAGCGTA[C/G]CATACTGACACCTAC | 79654 |
rs777831720 | snp | A/C | 3.43991e-05 | 0.00414709 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009705 | AGGGGCAGAGACGTG[A/C]AGTCAGCAGTTACCC | 79654 |
rs777916709 | snp | A/G | 8.35722e-05 | 0.00646368 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009325 | TTCAAGCTGGGCTAG[A/G]CTTGGAACATGCCCT | 79654 |
rs777925480 | snp | C/T | 1.65729e-05 | 0.00287857 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008343 | TGGGTAGATAGACTG[C/T]AGCTAAAGAGTTTAG | 79654 |
rs777940767 | snp | A/G | 0.00023832 | 0.0109134 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010514 | CTGGCCCGGCCTTCT[A/G]ACAGCCAGCCCCGCT | 79654 |
rs777945843 | snp | C/G | 1.66607e-05 | 0.00288619 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008498 | AAGGCTCAATGTTGG[C/G]GGAAGGGAAGGGCCC | 79654 |
rs778027053 | snp | A/G | 3.57577e-05 | 0.00422819 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010589 | AGAGCTGCTGCTGCC[A/G]CTGGAGGTGGTTGGG | 79654 |
rs778157222 | snp | C/T | | | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011453 | TTACTTATCTCTGTG[C/T]CACCCTAACCCAGCC | 79654 |
rs778218766 | snp | C/T | 3.33483e-05 | 0.00408327 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007388 | TGACTGATCCTATCT[C/T]AGTCGGACCCTAGGT | 79654 |
rs778287377 | snp | C/T | | | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45009416 | GTTGTCCCCTTCACC[C/T]CCATAGACCACCACC | 79654 |
rs778423869 | snp | A/G | 1.65649e-05 | 0.00287788 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004391 | ACCTGGGGAGTGGGT[A/G]AAAAGGCTTGGCTGG | 79654 |
rs778468212 | snp | A/G | 1.65592e-05 | 0.00287738 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45004675 | CCCATATCCCACGAC[A/G]ATGCCTGCACCCCCA | 79654 |
rs778483688 | snp | A/G | 0.00015829 | 0.00889495 | upstream-variant-2KB, synonymous-codon | UROD, HECTD3 | GRCh38.p7 | 1:45011132 | CACCTCTCGCGGCAC[A/G]AAAGCCAGCGCTGCT | 79654 |
rs778524509 | snp | C/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45006568 | CGGCTTCCCAAAGTG[C/G]TGGGATTACAGGCGT | 79654 |
rs778602943 | in-del | -/TG | 1.65927e-05 | 0.00288029 | upstream-variant-2KB, frameshift-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010261 | CTCGATCCCAGGCGA[-/TG]TGAGTATGTCAGGTC | 79654 |
rs778664311 | in-del | -/G | 1.65886e-05 | 0.00287993 | frameshift-variant | HECTD3 | GRCh38.p7 | 1:45006016 | ACTCCTTACCCCGAA[-/G]GGGCAGCCCCCATCA | 79654 |
rs778673234 | snp | G/T | 1.66593e-05 | 0.00288607 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003457 | GCCAAGAGGGACACG[G/T]GCAGTCTTGCTGGTC | 79654 |
rs778676104 | snp | C/T | 6.6268e-05 | 0.00575583 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004572 | GGAGGGGCCAAAGCT[C/T]TCTGCTCTACTAGCC | 79654 |
rs778710452 | snp | C/T | 1.89424e-05 | 0.00307748 | | | GRCh38.p7 | 1:45012883 | GCATACTGACACCTA[C/T]CCCCACCCCCACCTG | 79654 |
rs778786898 | snp | A/G | 1.65996e-05 | 0.00288089 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008357 | GCAGCTAAAGAGTTT[A/G]GCATACCTGTAACAC | 79654 |
rs778834357 | snp | A/G | 1.81145e-05 | 0.00300947 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010527 | CTGACAGCCAGCCCC[A/G]CTCCTTCAAGTGCAG | 79654 |
rs778919542 | snp | C/G | 8.2689e-05 | 0.00642944 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012971 | TGGGGAGAGGAAACA[C/G]ACTACACTCCCGTTT | 79654 |
rs778922305 | snp | A/G | 0.000181455 | 0.00952338 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010598 | GCTGCCGCTGGAGGT[A/G]GTTGGGAGTGTCGAT | 79654 |
rs778966009 | snp | A/C | | | missense | HECTD3 | GRCh38.p7 | 1:45004686 | CGACGATGCCTGCAC[A/C]CCCAGGGATCAGCTC | 79654 |
rs779036061 | snp | A/G | 3.33306e-05 | 0.00408218 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004032 | GCAGAGTCCAAACCC[A/G]GGTGTCACCCTGCCC | 79654 |
rs779074362 | snp | C/T | 1.65737e-05 | 0.00287864 | missense | HECTD3 | GRCh38.p7 | 1:45007519 | ATGAAGCTGGGCTTG[C/T]TGCTCTCAGAGTCAC | 79654 |
rs779122007 | snp | C/T | 3.36882e-05 | 0.00410402 | missense | HECTD3 | GRCh38.p7 | 1:45006705 | ACCTGGTTGGCTGTG[C/T]GTACAAAGAAGGGCA | 79654 |
rs779178220 | snp | A/G | 1.66452e-05 | 0.00288484 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009532 | AACCCACAGGGACAT[A/G]GCCCACCCACCCTGT | 79654 |
rs779282305 | snp | A/G | 1.70237e-05 | 0.00291746 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007603 | TTCACTTGCTAGTGA[A/G]GAGAGGTGGCCAGAG | 79654 |
rs779369552 | snp | A/T | 0.000124778 | 0.00789768 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012135 | TGGAGCTGTCGCTGG[A/T]GTCCGATCATGTGAT | 79654 |
rs779413535 | snp | G/T | 1.65636e-05 | 0.00287776 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004588 | TCTGCTCTACTAGCC[G/T]CTGGGTACTACCTGC | 79654 |
rs779427524 | in-del | -/TGTG | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45007131 | CCTCGAGCAGTTGTG[-/TGTG]TGTGTGTGTGTGTGT | 79654 |
rs779444949 | snp | C/T | 1.72812e-05 | 0.00293944 | synonymous-codon, intron-variant | HECTD3 | GRCh38.p7 | 1:45010106 | GCACTCGTAGGTCCA[C/T]GTCGGGGGTACATAG | 79654 |
rs779501074 | snp | C/G | 2.01912e-05 | 0.00317729 | upstream-variant-2KB, synonymous-codon | UROD, HECTD3 | GRCh38.p7 | 1:45011156 | CGCTGCTGGCAGCGG[C/G]CGCCCGGCGCGGAGG | 79654 |
rs779612022 | snp | A/G | 1.65614e-05 | 0.00287757 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003659 | AAATCGAGCCTAGGA[A/G]AAAACCCACCTGGCA | 79654 |
rs779654418 | snp | C/G | 4.96792e-05 | 0.00498368 | missense | HECTD3 | GRCh38.p7 | 1:45008606 | GTGGATATCGCACCA[C/G]ACTAGTTGGCTGGAA | 79654 |
rs779656537 | snp | A/G | 1.81939e-05 | 0.00301606 | synonymous-codon, intron-variant | HECTD3 | GRCh38.p7 | 1:45009995 | ACCCACCGTGTAGGA[A/G]GAAACGTCTATGCTC | 79654 |
rs779696059 | snp | A/T | 1.65652e-05 | 0.0028779 | missense | HECTD3 | GRCh38.p7 | 1:45007489 | GCAAGACGGCGGTTG[A/T]TGTATAGGCGTGGCA | 79654 |
rs779707283 | in-del | -/A | 1.64773e-05 | 0.00287026 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012256 | AGCTCGCAGTTACAG[-/A]CAGCTGACCATGGAA | 79654 |
rs779740223 | snp | C/G | 6.68986e-05 | 0.00578315 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45006716 | TGTGCGTACAAAGAA[C/G]GGCAGGGGCACGGGG | 79654 |
rs779819220 | snp | C/T | 1.66313e-05 | 0.00288364 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008521 | AAGGGCCCATAGGTC[C/T]AGGACCACAGCCACC | 79654 |
rs779819986 | snp | A/G | 1.92691e-05 | 0.0031039 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010614 | GTTGGGAGTGTCGAT[A/G]GGTACCAGGCGGGCT | 79654 |
rs779828138 | snp | A/C/T | | | upstream-variant-2KB, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45011349 | CACCACGCCCTTCCC[A/C/T]GCCTTTGGCCAGCCT | 79654 |
rs779839902 | snp | A/G | 1.67638e-05 | 0.0028951 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006131 | CCTGCCCCAGAGACA[A/G]AGCTGTGAGTGTGGC | 79654 |
rs780004662 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45007850 | AGTCCTTGCTTCACA[A/G]CCTGGCCCACAGGGC | 79654 |
rs780100484 | snp | A/G | 3.4089e-05 | 0.00412836 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010712 | CCAGCTGCTCCTGCC[A/G]GGACGCGTAGGATGG | 79654 |
rs780111467 | snp | G/T | 1.64936e-05 | 0.00287168 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013099 | GGAGGGCTCTGGAGG[G/T]CCTCAAGGCTGAGCC | 79654 |
rs780126586 | snp | C/G | 6.99142e-05 | 0.00591204 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007628 | CCAGAGCAGGAATGA[C/G]TGGGCAGTCAGCCTC | 79654 |
rs780134261 | snp | C/T | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45009866 | GATGGGGAGCTGAAC[C/T]GAGTGTGGCCTGTGG | 79654 |
rs780188982 | snp | A/C | | | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011394 | GGACTAAGCGCACCC[A/C]AGCTCTCACTGTATT | 79654 |
rs780272957 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45004214 | CCTGTGCTGTGCTGT[A/G]CTGCCCTGCCCTGCC | 79654 |
rs780292372 | snp | G/T | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45007870 | GCCCACAGGGCCCTC[G/T]GCAACCAGGACCTGT | 79654 |
rs780339962 | snp | C/T | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003365 | TACCCCAACTGCACA[C/T]AGGAGCAGGGCACAT | 79654 |
rs780373757 | snp | C/T | 3.34174e-05 | 0.00408749 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003841 | GCACCTTCAGGCCTC[C/T]CTCCAGCACTCACCC | 79654 |
rs780382912 | snp | A/G | 1.74321e-05 | 0.00295224 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005890 | GGCCAGGACCTGTGT[A/G]ACAAACACTCCCCAC | 79654 |
rs780466778 | snp | C/G | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002615 | AGTGTCACGGAGGCC[C/G]TGAGGGAGGAACGGT | 79654 |
rs780488393 | snp | A/G | 1.65745e-05 | 0.00287871 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45009157 | ACCTCGGCACTCCAC[A/G]ATGCGGATCTCGATG | 79654 |
rs780522414 | snp | A/G | 3.31494e-05 | 0.00407107 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010224 | TTGTACAGCTTCTGC[A/G]TATGCCTCTGCCGGC | 79654 |
rs780540144 | snp | C/T | 3.29451e-05 | 0.00405851 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013289 | GTCTCCTGTTTCCTA[C/T]AGCCACTGCGTCGCT | 79654 |
rs780590995 | snp | A/C | 1.67189e-05 | 0.00289122 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009093 | ACACTCTCTGTTTGC[A/C]CCCATCTCCACGCCG | 79654 |
rs780613816 | snp | C/T | 1.78931e-05 | 0.00299102 | missense, intron-variant | HECTD3 | GRCh38.p7 | 1:45010087 | AGTGGATCAGGTCCT[C/T]GTCGCACTCGTAGGT | 79654 |
rs780682133 | snp | C/T | | | downstream-variant-500B | HECTD3 | GRCh38.p7 | 1:45002314 | TCCTCCAAATCACCA[C/T]ATCCATGCCAGAAAA | 79654 |
rs780700915 | in-del | -/CCAAAAA | | | downstream-variant-500B | HECTD3 | GRCh38.p7 | 1:45002157 | AAAAAGGACTGCAAC[-/CCAAAAA]GGGTTGGGGGCAGGG | 79654 |
rs780701612 | snp | A/G | 6.62405e-05 | 0.00575464 | missense | HECTD3 | GRCh38.p7 | 1:45008621 | GACTAGTTGGCTGGA[A/G]CAGGTCTGCATTCAA | 79654 |
rs780794907 | snp | A/G | 1.66208e-05 | 0.00288273 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006917 | TTGATAGGGCAGCAA[A/G]CAGGACCCTTGAGAT | 79654 |
rs780801700 | snp | C/T | 1.65723e-05 | 0.00287852 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010183 | TCCTTCCTCCCCACC[C/T]CATTCCAGCTCACTC | 79654 |
rs780839394 | snp | A/G | 1.65647e-05 | 0.00287786 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004818 | TCACCTAGGGGTTGG[A/G]GAGAGGCAGGGAGGT | 79654 |
rs780884717 | snp | C/T | 3.31499e-05 | 0.0040711 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004245 | CTGCCTTGGGGAACT[C/T]ACTGAGCTTGCGCAG | 79654 |
rs780936179 | snp | C/T | 1.66796e-05 | 0.00288782 | missense | HECTD3 | GRCh38.p7 | 1:45006727 | AGAAGGGCAGGGGCA[C/T]GGGGGTATCCGCTGA | 79654 |
rs780950399 | snp | A/G | 1.6656e-05 | 0.00288578 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004155 | GGAGACAAGGCCAGC[A/G]TTCATTCTTGGGTCT | 79654 |
rs780968491 | snp | A/C | 1.6628e-05 | 0.00288335 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009555 | CACCCTGTCCTGCCC[A/C]GAGCCTACTTACTTG | 79654 |
rs781006632 | snp | C/T | 1.64882e-05 | 0.00287121 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013115 | CCTCAAGGCTGAGCC[C/T]TGTCTTCCCTCTGTA | 79654 |
rs781024443 | snp | G/T | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45005648 | TTTAGGGGTCACGAG[G/T]CTACAGACAGTAGTT | 79654 |
rs781094801 | snp | A/C | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013254 | AAGATTTATGCCTTC[A/C]GTCTGCCACCTAGCA | 79654 |
rs781154736 | snp | A/G | 1.65701e-05 | 0.00287833 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008338 | TGGCATGGGTAGATA[A/G]ACTGCAGCTAAAGAG | 79654 |
rs781243159 | snp | A/C | 1.64792e-05 | 0.00287042 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012295 | GTTGGGGTGAGTTCT[A/C]CAGAGCACGCGGTGT | 79654 |
rs781243427 | snp | A/C | 1.6569e-05 | 0.00287824 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45004357 | TACCACCTTCAGCAG[A/C]CCTGCCTGCATAGCT | 79654 |
rs781254415 | snp | A/G | 1.97178e-05 | 0.00313983 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010882 | TCCTGGGCAGGGAAG[A/G]GCGCACCTTTGTCAG | 79654 |
rs781257540 | snp | A/C | 1.65833e-05 | 0.00287948 | missense, utr-variant-5-prime | HECTD3 | GRCh38.p7 | 1:45009620 | AGTGTTGGCACTGGG[A/C]CCCATCGCTCTCCCA | 79654 |
rs781273907 | snp | G/T | 0.0187051 | 0.0948825 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008231 | CCAGCACTGGCTGGG[G/T]CGGCTCACCTTAATC | 79654 |
rs781278533 | snp | C/G/T | 3.47145e-05 | 0.00416609 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005914 | TCCCCACTGTCTTCT[C/G/T]ACCCTGAGCTGCCCA | 79654 |
rs781329350 | snp | A/G | 1.66263e-05 | 0.00288321 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010306 | CACCTGTGGGCACAG[A/G]GTAGGGAGTGGGATG | 79654 |
rs781438956 | snp | A/T | 0.000198797 | 0.0099679 | intron-variant | HECTD3 | GRCh38.p7 | 1:45003776 | TAGGTCAGGAAGATG[A/T]GTTGGGGCACATGTA | 79654 |
rs781527141 | snp | C/T | 1.66921e-05 | 0.00288891 | missense | HECTD3 | GRCh38.p7 | 1:45003882 | GGGTAGATGTAGATC[C/T]GTGCTGGCAGGCGAC | 79654 |
rs781536517 | snp | G/T | 2.57735e-05 | 0.00358972 | intron-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012863 | TTTCCCCAGCCTCCA[G/T]CGTAGCATACTGACA | 79654 |
rs781538521 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45004960 | TACAAGAGCTGTAAA[A/G]GCATCAAGACAACAC | 79654 |
rs781621513 | snp | A/C | | | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012560 | TGGGTATTTCTCAGC[A/C]CCTGAACCAGCCCAG | 79654 |
rs781633161 | snp | A/G | 3.31494e-05 | 0.00407107 | missense | HECTD3 | GRCh38.p7 | 1:45009176 | CGGATCTCGATGATC[A/G]GGAGGTGGACGGTCA | 79654 |
rs781675937 | snp | C/G/T | 4.65799e-05 | 0.00482574 | upstream-variant-2KB, missense | UROD, HECTD3 | GRCh38.p7 | 1:45010999 | CGGCGCGGAGGGGCC[C/G/T]GGAGCCGGTACCGGG | 79654 |
rs796388421 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45011269 | CCATGGCGAAGTGGC[A/G]GAGGTGAGCACCTAG | 79654 |
rs796428831 | snp | C/T | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45006657 | TAGCTCAATCTGGCA[C/T]CTGGGAGGTTTGCAG | 79654 |
rs796893910 | snp | A/G | | | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011910 | TCCAGGCTATAGTAT[A/G]GACCTGGCTGGATAA | 79654 |