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 |