SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs5869 | snp | C/T | 0 | 0 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002936 | TTTCCCCTCTCCCTC[C/T]ACACCAGAGATGTGG | 79654 |
rs8681 | snp | C/T | 0.441158 | 0.161117 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002934 | TCCCCTCTCCCTCCA[C/T]ACCAGAGATGTGGTG | 79654 |
rs884581 | snp | C/T | 0.0640965 | 0.167152 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011973 | TCTCATCTGACAGTC[C/T]GGGTATCCGGAGGCT | 79654 |
rs884582 | snp | G/T | | | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011953 | ATCCGGAGGCTTGGC[G/T]CAAGTCCCACTCATG | 79654 |
rs885843 | snp | G/T | 0 | 0 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012053 | TGGGCCTTTGTTGTT[G/T]CGTCGCTACAGCAAA | 79654 |
rs1131147 | snp | C/T | 0 | 0 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45013308 | CACTGCGTCGCTTCC[C/T]TCTGGATGCTGCCAT | 79654 |
rs1804885 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012955 | ATTCCTGCGAGCAGC[C/T]TGGGGAGAGGAAACA | 79654 |
rs2236576 | snp | A/T | 0.376592 | 0.215579 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012003 | ATGTATCTTACGGTG[A/T]CATGAGGAATTTGTT | 79654 |
rs2275598 | snp | C/G | 0.436692 | 0.166271 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009083 | ATGGGGGCAAACAGA[C/G]AGTGTGTGTGGAGAG | 79654 |
rs2275599 | snp | A/T | 0.436692 | 0.166271 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009078 | GGCAAACAGAGAGTG[A/T]GTGTGGAGAGAAGAG | 79654 |
rs2298005 | snp | C/T | 0.438154 | 0.164615 | upstream-variant-2KB, synonymous-codon | UROD, HECTD3 | GRCh38.p7 | 1:45010991 | CGGCTCCGGGCCCCT[C/T]CGCGCCGCCCGCGAC | 79654 |
rs2298006 | snp | C/T | 0.461122 | 0.133894 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008485 | CCCCCAACATTGAGC[C/T]TTGTGTGTCTGCATG | 79654 |
rs3806405 | snp | A/G | 0.436692 | 0.166271 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010817 | CTCAATACAGGGGAG[A/G]AAAGGCAAACAGCCA | 79654 |
rs4072040 | snp | A/T | | | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011761 | GTTGAGTTCTGTTTG[A/T]CACTCCTAATCCCAA | 79654 |
rs4660829 | snp | A/T | 0.0150606 | 0.0854603 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002959 | AGGGGAAAAGAGCAG[A/T]ATGTGAGGGCAGGTG | 79654 |
rs4660830 | snp | C/T | 0.4436 | 0.159329 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007644 | TGGGCAGTCAGCCTC[C/T]GTCCAGGCCCTGGAA | 79654 |
rs6429552 | snp | A/G | 0 | 0 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009894 | TGGGGACCCTGTTTT[A/G]GTCCTGGCCTGCAGG | 79654 |
rs6674839 | snp | A/G | 0 | 0 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005382 | GAGACAGGAAAAGCA[A/G]ACAGATTACAGAGGA | 79654 |
rs7415602 | snp | C/G | | | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011544 | ACTACCATTTTATCT[C/G]TACTGCTACTACCCT | 79654 |
rs7521006 | snp | C/T | 0.457969 | 0.138741 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006497 | TTTATAGAGATGGGG[C/T]TTCACTTCATTGGCC | 79654 |
rs7528534 | snp | C/T | 0.185788 | 0.241613 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004458 | ATCACTGTGGCCTTT[C/T]AGCAGCAGAAAGGTG | 79654 |
rs7533668 | snp | A/C | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010397 | TATCTCCCAGTCTCC[A/C]TCCGAGCCCCCTTCA | 79654 |
rs7536892 | snp | G/T | 0.0343835 | 0.126529 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012132 | CCCTGGAGCTGTCGC[G/T]GGAGTCCGATCATGT | 79654 |
rs7541207 | snp | C/T | 0.382031 | 0.212292 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008336 | TCTGGCATGGGTAGA[C/T]AGACTGCAGCTAAAG | 79654 |
rs11211065 | snp | A/G | 0.0349064 | 0.127416 | intron-variant | HECTD3 | GRCh38.p7 | 1:45004831 | GGAGAGAGGCAGGGA[A/G]GTAACCTTTTCACTG | 79654 |
rs11355812 | in-del | -/T | 0.371582 | 0.218444 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007901 | CTCCTGCCCACATCC[-/T]TCCACCCTCATCCCT | 79654 |
rs11541959 | snp | A/G | 0 | 0 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012929 | GGTTTTCCGGAGCTG[A/G]AGAATGACACATTCC | 79654 |
rs11541964 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, missense | UROD, HECTD3 | GRCh38.p7 | 1:45013351 | CATCCTTGTTGTACC[C/T]CAGGCACTGGGCATG | 79654 |
rs11541966 | snp | C/T | 1.65586e-05 | 0.00287733 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012956 | TTCCTGCGAGCAGCC[C/T]GGGGAGAGGAAACAG | 79654 |
rs11541967 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012927 | AGGGTTTTCCGGAGC[C/T]GAAGAATGACACATT | 79654 |
rs11548988 | snp | C/T | | | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45003863 | CTACATCTACCCAGA[C/T]AAGCTGGGCTACGAG | 79654 |
rs11548989 | snp | A/T | | | missense, intron-variant | HECTD3 | GRCh38.p7 | 1:45010002 | ATGTGGAGAGCATAG[A/T]CGTTTCCTCCTACAC | 79654 |
rs11548990 | snp | C/T | 0.129772 | 0.219236 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003483 | TGGTCCCACAGCCGG[C/T]GGCACGCCTCACTCC | 79654 |
rs12036125 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005017 | gcatcctgtggaaaa[C/T]ggtgtctcagctgag | 79654 |
rs12084469 | snp | A/G | 0.131381 | 0.220067 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011974 | GCCTCCGGATACCCA[A/G]ACTGTCAGATGAGAA | 79654 |
rs12134146 | snp | C/T | 0.436408 | 0.16659 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007720 | TAGTCCATCCCTGTC[C/T]TTGTCTCCAGTCCCC | 79654 |
rs12739545 | snp | A/G | 0.371582 | 0.218444 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005690 | AGTGGATGGATTGGA[A/G]AGGGATCTTGTGTGT | 79654 |
rs12749251 | snp | A/T | 0.194013 | 0.24365 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45003504 | GCCTCACTCCTCCCA[A/T]GGGCTCATGTCAGTG | 79654 |
rs12749939 | snp | C/T | 0.376195 | 0.215812 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012761 | TAGGCAGAGAGGAGG[C/T]GGAACGGGCGGAAAG | 79654 |
rs28582938 | snp | C/G | 0.0060304 | 0.0545787 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006811 | CTGAAATGACAGATG[C/G]CCTCAGCTGGGCACT | 79654 |
rs35389227 | in-del | -/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45008200 | CTACGTGAGCAGGAA[-/G]GGGGAAATGCCAAGA | 79654 |
rs35563981 | in-del | -/G | | | upstream-variant-2KB, frameshift-variant | UROD, HECTD3 | GRCh38.p7 | 1:45011011 | CCCGGAGCCGGTACC[-/G]GGGGGCTGGGCCTGC | 79654 |
rs35640500 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013029 | ACCAGGTAAGAGTCA[-/G]GGGTCTGGAAATCTA | 79654 |
rs35657340 | in-del | -/C | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003192 | TGGGGACCTAGATGG[-/C]CCCCTTCAAGTAGCT | 79654 |
rs41269095 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003326 | GCTGGGCCACTAGTG[A/T]TACCTGACCATGCCA | 79654 |
rs41269097 | snp | C/T | 0.00833449 | 0.0640139 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010214 | ACAGTAGCCTTTGTA[C/T]AGCTTCTGCGTATGC | 79654 |
rs41269099 | snp | A/G | 0.00463413 | 0.0479123 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010256 | GAGGTCTCGATCCCA[A/G]GCGATGTGAGTATGT | 79654 |
rs41269101 | snp | A/G | 0.00890732 | 0.0661387 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010335 | TGGGGAGACATCAGC[A/G]GTCAGCAAGACACTA | 79654 |
rs41269103 | snp | A/C | 0.00165041 | 0.0286789 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UROD, HECTD3 | GRCh38.p7 | 1:45012214 | GGACTGGGGGGCAGG[A/C]TCAGATTCAGGTTAA | 79654 |
rs41312020 | snp | A/G | 0.130604 | 0.21965 | synonymous-codon | HECTD3 | GRCh38.p7 | 1:45003914 | GCGGCCCGTGACAAA[A/G]CGCAGGAAGCGGCTC | 79654 |
rs55841688 | snp | A/G | 0.146395 | 0.227522 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010727 | GGGACGCGTAGGATG[A/G]GGACAGCCGTCAGGG | 79654 |
rs56089917 | snp | A/G | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45008975 | TTAAGGCAGGCCTAT[A/G]CCTGGCATGTCCCAG | 79654 |
rs56343463 | in-del | -/GTGT | 0 | 0 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007154 | TGTGTGTGTGTGTGT[-/GTGT]TTGTGTGTGTTTGTG | 79654 |
rs60060850 | snp | C/T | 0.130694 | 0.219696 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007943 | ACACCTACTGGCACA[C/T]TTTTCTCAAGACATC | 79654 |
rs61741088 | snp | A/G | 0.0405423 | 0.136482 | synonymous-codon, utr-variant-5-prime | HECTD3 | GRCh38.p7 | 1:45009606 | AGTAAGCCGTACCCA[A/G]TGTTGGCACTGGGAC | 79654 |
rs61790640 | snp | G/T | 0.0158719 | 0.0876587 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007158 | TGTGTGTGTGTGTGT[G/T]TGTGTGTGTTTGTGT | 79654 |
rs61790641 | snp | G/T | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45007162 | TGTGTGTGTGTTTGT[G/T]TGTGTTTGTGTGCAC | 79654 |
rs71896015 | in-del | -/TGTG | | | intron-variant | HECTD3 | GRCh38.p7 | 1:45007127 | GGTGCCTCGAGCAGT[-/TGTG]TGTGTGTGTGTGTGT | 79654 |
rs72887047 | snp | C/T | 0.0407008 | 0.136725 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007392 | TGATCCTATCTCAGT[C/T]GGACCCTAGGTGGTG | 79654 |
rs72887050 | snp | A/G | 0.0398582 | 0.135427 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008393 | ACTCCCCAACATAAA[A/G]GGACAGGAAAAGGCA | 79654 |
rs72887057 | snp | C/G | 0.131381 | 0.220067 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011446 | AACCATATTACTTAT[C/G]TCTGTGCCACCCTAA | 79654 |
rs72887059 | snp | C/T | 0.131723 | 0.220251 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011569 | TACCCTCATTCAAGT[C/T]ACCATTCTAGCTAGC | 79654 |
rs74070824 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008088 | CCTCCCAAACACTAA[A/G]TTTGGACCATTTGTT | 79654 |
rs74070825 | snp | A/C | 0.000281968 | 0.0118703 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008352 | AGACTGCAGCTAAAG[A/C]GTTTAGCATACCTGT | 79654 |
rs75233868 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | HECTD3 | GRCh38.p7 | 1:45002528 | TAAGCCCAGGGCCCA[A/G]TAAACACATTCTGAA | 79654 |
rs75586344 | snp | C/T | 6.62361e-05 | 0.00575445 | missense | HECTD3 | GRCh38.p7 | 1:45004674 | CCCCATATCCCACGA[C/T]GATGCCTGCACCCCC | 79654 |
rs76154101 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007108 | AAAAGCAGTCATGGC[C/G]AGGGGTGCCTCGAGC | 79654 |
rs76297558 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006224 | TTCCACTAAATGATC[C/T]CTTCAAATGCACAGT | 79654 |
rs76750365 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008165 | GAGTAGATTTTAGGA[A/G]CTCTGCTAAGGAATG | 79654 |
rs77867663 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002693 | AGGCTTTAGAGTTGG[A/G]GAAAGGGGAGCTATT | 79654 |
rs77868201 | snp | C/T | 0.0090199 | 0.0665477 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007205 | CGAGTAAGTCCCTCA[C/T]TCTCATGCCATACCT | 79654 |
rs78370467 | snp | C/T | 0.0131041 | 0.0798768 | upstream-variant-2KB, synonymous-codon | UROD, HECTD3 | GRCh38.p7 | 1:45010898 | GCGCACCTTTGTCAG[C/T]TTCACCCAGAGCCCG | 79654 |
rs78731459 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003447 | CCTGGGCAAGGCCAA[A/G]AGGGACACGTGCAGT | 79654 |
rs78779774 | snp | A/G | 0.00423549 | 0.0458236 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008192 | AATGAACAACTACGT[A/G]AGCAGGAAGGGGAAA | 79654 |
rs79038092 | snp | A/G | | | missense | HECTD3 | GRCh38.p7 | 1:45003700 | GGAAGAGGGTGCTGG[A/G]GCAAGTGGAAGACTC | 79654 |
rs79450945 | snp | C/T | 0.000678847 | 0.0184109 | missense | HECTD3 | GRCh38.p7 | 1:45003724 | AAGACTCGGGCAGCG[C/T]GTCTGTGGTCTCGTA | 79654 |
rs79965635 | snp | A/C | | | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45013288 | TGTCTCCTGTTTCCT[A/C]CAGCCACTGCGTCGC | 79654 |
rs111530541 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012115 | GGCAGCAGCCAGGGC[A/G]GCCCTGGAGCTGTCG | 79654 |
rs111608474 | snp | A/G/T | 0 | 0 | splice-acceptor-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012905 | CCCCACCTGATCGCC[A/G/T]GACCTCAGGGTTTTC | 79654 |
rs112059352 | snp | A/G | 0.0174175 | 0.0916809 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012026 | AGATACATTTACAGC[A/G]GAGTTTTCTTTTGGG | 79654 |
rs112248598 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006463 | GGCGCGTGCCACCAC[A/G]CCCGGCTAATTTTTT | 79654 |
rs112770839 | snp | C/T | 0 | 0 | intron-variant | HECTD3 | GRCh38.p7 | 1:45008070 | AAGGAGGCTGGGGAA[C/T]AGCCTCCCAAACACT | 79654 |
rs113059779 | in-del | -/T | 0 | 0 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006307 | CCTCTGCCCTATTTC[-/T]ATTTTTTTTTTTTTT | 79654 |
rs113092319 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45012365 | CTCTATCCCTCTACT[C/G]CCCTTTCCCCACCCT | 79654 |
rs113135392 | snp | C/T | 1.67329e-05 | 0.00289243 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006120 | AGTGCCATTGCCCTG[C/T]CCCAGAGACAGAGCT | 79654 |
rs113246343 | snp | A/C | | | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45002717 | AGCTATTACAGATTT[A/C]AAAAAGGCCATAACT | 79654 |
rs113281901 | snp | C/G/T | 1.69795e-05 | 0.00291367 | intron-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45012904 | CCCCCACCTGATCGC[C/G/T]AGACCTCAGGGTTTT | 79654 |
rs113451625 | snp | A/G | 0.0398555 | 0.135423 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003489 | CACAGCCGGCGGCAC[A/G]CCTCACTCCTCCCAA | 79654 |
rs113562836 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | UROD, HECTD3 | GRCh38.p7 | 1:45010359 | GACACTACCTCCATG[C/T]CGTGTAGCCTTCTTC | 79654 |
rs113744661 | snp | C/T | 0.000116018 | 0.00761548 | upstream-variant-2KB, missense, utr-variant-5-prime | UROD, HECTD3 | GRCh38.p7 | 1:45010223 | TTTGTACAGCTTCTG[C/T]GTATGCCTCTGCCGG | 79654 |
rs114215565 | snp | A/G | 0.00115187 | 0.023971 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009320 | AGGCTTTCAAGCTGG[A/G]CTAGGCTTGGAACAT | 79654 |
rs114224533 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | HECTD3 | GRCh38.p7 | 1:45002406 | CTCAGCCCCAGATAT[A/G]TAACTGTGCAAAGTC | 79654 |
rs114902613 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B | HECTD3 | GRCh38.p7 | 1:45002081 | AGTAAGCCGTGACTG[C/T]ACCACTACACGCCAG | 79654 |
rs115168232 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011828 | CTGATTTCTGTTTCC[C/G]CAGTCTTGTAGCTCC | 79654 |
rs115482262 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | HECTD3 | GRCh38.p7 | 1:45005643 | AGGATTTTAGGGGTC[A/T]CGAGTCTACAGACAG | 79654 |
rs116027330 | snp | A/G | 0.0236746 | 0.106192 | upstream-variant-2KB | UROD, HECTD3 | GRCh38.p7 | 1:45011776 | TCACTCCTAATCCCA[A/G]GGACACTGGAGATCA | 79654 |
rs116356408 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | HECTD3 | GRCh38.p7 | 1:45006508 | GGGGCTTCACTTCAT[C/T]GGCCAGGCTGGTCTT | 79654 |
rs116411210 | snp | C/T | 0.00188572 | 0.0306481 | intron-variant | HECTD3 | GRCh38.p7 | 1:45007633 | GCAGGAATGAGTGGG[C/T]AGTCAGCCTCCGTCC | 79654 |
rs116477746 | snp | C/T | 0.00101459 | 0.0225004 | utr-variant-3-prime | HECTD3 | GRCh38.p7 | 1:45003467 | ACACGTGCAGTCTTG[C/T]TGGTCCCACAGCCGG | 79654 |
rs116721425 | snp | C/T | 9.97738e-05 | 0.00706236 | intron-variant | HECTD3 | GRCh38.p7 | 1:45009120 | GCCGGGCTCTCTTTC[C/T]CTCCTTATAGCCTTA | 79654 |