SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs143363110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118464 | TTAAGCTTTTTAACT[A/G]CCTTGTCAAACAGGG | 25831 |
rs143364425 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153840 | CAAAAAAAGAAATGA[C/T]ACAAATATATATATA | 25831 |
rs143376982 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120427 | ATTCACAAACATCCT[A/C]AATTTCCTGGCTTTG | 25831 |
rs143394834 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161702 | GCAGGCAGATCACCC[A/G]AGATGAGGAGTTCGA | 25831 |
rs143397601 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159604 | CTCAGCCTCCAAAGC[A/G]CTGGGATTACAGGCG | 25831 |
rs143401795 | snp | G/T | 6.65646e-05 | 0.0057687 | missense | HECTD1 | GRCh38.p7 | 14:31116441 | CGACTTCTTCCAAGA[G/T]CTCTGAATGAGGGGT | 25831 |
rs143404862 | snp | A/G | 3.31647e-05 | 0.00407201 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148920 | GTTTCTGCAGTAAAT[A/G]AATGTTTGGTTCCTC | 25831 |
rs143444400 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187972 | TGTTGGCTAGGCTGG[C/T]CTCAAACTCCAGACC | 25831 |
rs143453140 | in-del | -/AG | 0.0248432 | 0.108648 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209313 | CCAACAGTAAGCAAC[-/AG]AGAGAGAAATTTGGA | 25831 |
rs143500691 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166593 | CGGTAGCTCATGCCT[A/G]TAATTCCAGCACTTC | 25831 |
rs143529946 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152715 | AAAAATAAAATAAAT[-/A]TTTTTTTAATTAAAC | 25831 |
rs143562391 | snp | C/T | 0.00294393 | 0.0382531 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106611 | TTTAAAACTTATTCA[C/T]GCATTGGATTGAAGA | 25831 |
rs143573447 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203493 | ACATTATAAAGCCAG[G/T]TGTGGTGGCACAGCC | 25831 |
rs143582391 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147205 | GTAGTCCCAGCTACT[C/T]GGAAGGCTGAGGCAG | 25831 |
rs143684129 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204122 | GGTGTATATGTGCCA[C/T]GTTTGCTTAATCCAG | 25831 |
rs143691459 | in-del | -/ACTT | 0.0633504 | 0.166319 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171737 | AAACTAATTAAAAAC[-/ACTT]ACAGTGAGTAAGGGG | 25831 |
rs143710464 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189715 | AGGTAGAGGCTGCAG[C/T]GAGCTGCATTCCAGC | 25831 |
rs143776940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134082 | AAAGAGTAGGAGAAA[C/T]TCTCTTATGATGGAA | 25831 |
rs143820738 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194201 | AAAAGTCAAAACTAT[A/T]TCAACAGAAAACAGG | 25831 |
rs143821977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130383 | AAGCTAATAACATGT[A/G]CAGAATTAACGAGCA | 25831 |
rs143827390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200400 | CCTGTAATCCCAGCA[C/T]TCTGGAAGGCCAAGG | 25831 |
rs143861249 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136799 | ACTATGAACAAATGT[C/T]TGTTTTCTATCAAAG | 25831 |
rs143864925 | snp | G/T | 0.0287284 | 0.116357 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207084 | CGAGAGGAGGCCGCC[G/T]GGCCAGGCAGGGCGC | 25831 |
rs143937582 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118228 | GTCAGGCTGGTCTTG[A/G]ACTCCTGACCTTGTG | 25831 |
rs143941889 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188128 | ATAGATAGATAGATA[C/G]ATAGATAGATAGATA | 25831 |
rs143953439 | snp | A/G | 6.85895e-05 | 0.00585577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128041 | AAATCAGTACAAATA[A/G]GTGAGATTGTAGAAA | 25831 |
rs144047352 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187710 | TAGCATGAGCCCTGT[A/G]GTGTTAGATTAGAAC | 25831 |
rs144111079 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121962 | TAACTCTGATGATAA[C/G]GGCAAATTTTTTTTT | 25831 |
rs144123754 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118794 | AGCTACTCAGGAGGC[A/G]GAGGCAGGAGAATTG | 25831 |
rs144130954 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188299 | GGAGTGCAGTGACAC[A/G]ATCTCAGCTCACTTC | 25831 |
rs144154185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164455 | TGCTCCCCCTTGTTT[C/T]TAATAATGCTAAATA | 25831 |
rs144178422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114784 | TGCAGCATTAGGTGA[G/T]CTGGTGGTTGTGAAA | 25831 |
rs144218494 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111353 | CACTTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT | 25831 |
rs144238266 | in-del | -/TG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122379 | GTGTGTGTGCGCGCA[-/TG]TGTGTGTGTGTGTGT | 25831 |
rs144254312 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176161 | AAGCTCATAATAATA[C/T]TCTAACACTATTTGT | 25831 |
rs144269482 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177625 | AATAATGTCTAGCAC[C/T]GGTGGGTGGTGTTTG | 25831 |
rs144312135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206413 | GTTAGATTCAGTATT[C/T]TGAGGAAACTCTAAA | 25831 |
rs144354143 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109677 | GCAACAGAATTCAAA[A/G]ATTTAAGAAATTAAA | 25831 |
rs144387232 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135736 | TAACAAATGCTCATT[A/T]AGGCCGGGTGCGGTG | 25831 |
rs144426641 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132175 | GCGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 25831 |
rs144466974 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174799 | GAGGATGGAATTACC[C/T]CGATTTCATCAAGTG | 25831 |
rs144484148 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154587 | ACAGGCATGAGCCAC[G/T]GCACTCAGCCTAGAA | 25831 |
rs144502967 | snp | A/G | 0.030278 | 0.119257 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191917 | AGGAAGCTGAGGTAG[A/G]AGAATCGATTGAACT | 25831 |
rs144604853 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169940 | TATGAATTAATTGTA[C/G]TTGGTTATTTATCAT | 25831 |
rs144624777 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166043 | TAGAGACAGGGTTTC[A/G]CCACGTTAGCCAGGC | 25831 |
rs144628645 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195606 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGGTCAA | 25831 |
rs144640777 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31164799 | ACATTTAAAATGATA[A/G]AAGAAAATAACCATC | 25831 |
rs144647254 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202719 | ATTTATTAATGATGG[C/T]ATCAGTGGGTAGCCC | 25831 |
rs144647898 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108062 | CTTTTGTGTGTCTCT[-/G]GTGTGACACCAAAGC | 25831 |
rs144680744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199578 | AAATTAGCTGGACAC[A/G]GTGGCGCACACCTGT | 25831 |
rs144681403 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200583 | TCAGGAATTCGAGAC[C/T]AGCCTGGCCAACATA | 25831 |
rs144681527 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160492 | AGTACTGCATTCATA[C/T]TGGCAAACTGATTCA | 25831 |
rs144697594 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139362 | GATTAGTGTCCTTAT[A/T]AAAGAGGCCTGAGAG | 25831 |
rs144704055 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209839 | CCTCGAGGTCGAAGC[C/T]GCAGTGAGCCATGAT | 25831 |
rs144806886 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145403 | TGTGGTGGCTCATGC[G/T]TGTAATCCTAGCACT | 25831 |
rs144827033 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184661 | CAAGAGGATCACTTG[A/C]GCCCAGGAGTTCAAG | 25831 |
rs144843181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111959 | GCACTCCTGCCTGGG[C/T]GACAGAGCGAGACTC | 25831 |
rs144847112 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153073 | CCTTTTCTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 25831 |
rs144981723 | snp | C/T | 0.000538313 | 0.0163972 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149982 | AGGAAAATATTTTAA[C/T]TGAAACAAAATATTA | 25831 |
rs145036929 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111518 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT | 25831 |
rs145054087 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145785 | GCTACTGATTTCAAA[C/T]CAAGAAAGTGAAGCA | 25831 |
rs145058941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184349 | ATCCCAGCACTTTGG[A/G]AGGCCGAGCCAGGTG | 25831 |
rs145086606 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141324 | AAAGAATTATTTTTT[A/T]AAAAAAAACAGTATT | 25831 |
rs145162822 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201567 | GAGGCTGGAGTGCAA[C/T]GGCACAATCTTGGTT | 25831 |
rs145218773 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116756 | CTTCGTCAGCCTCCC[A/G]AGTAGCTGGGATTAT | 25831 |
rs145232094 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132390 | TGCAGTGAGCTGATA[C/T]TGCGCCATTGCACTC | 25831 |
rs145254984 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168817 | GGAGGCCGAGACGGG[C/T]GGATCACGAGGTCAG | 25831 |
rs145274251 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127415 | GGAGTGCAATGGCGC[G/T]ATCTCTGCTCACTGT | 25831 |
rs145288546 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198433 | CCAATCATAACACTC[A/C]ACTTTACAAGCAAAA | 25831 |
rs145323103 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194310 | GAAATGTTCTGCATT[C/T]CAATTATAGTGGTGG | 25831 |
rs145370280 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125943 | GCAATGTTTTTGGAA[A/C]GCAATTCAATAATTA | 25831 |
rs145408214 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122502 | CGTGTGTGTGTGTTT[A/G]TGTCATTCTGTGGCT | 25831 |
rs145413667 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101860 | GAACTAAAAAATACT[A/G]ACAGTGTATGGGGTC | 25831 |
rs145550599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165692 | TCAATCATTCAGTAA[A/G]TATCTACTGAGGACC | 25831 |
rs145609702 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186357 | CTGAGAATCATTCTT[C/G]ATTTCCCCCCATTTC | 25831 |
rs145637505 | snp | A/G | 0.079617 | 0.182947 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186880 | ATACAAAAATCAGCC[A/G]GACGTGGTGGCACAT | 25831 |
rs145657410 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183656 | TCCAATAATTTTGTG[A/T]CATCACTACTCAACT | 25831 |
rs145671836 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163442 | GTGAGCCCCTTTCCT[-/C]CCCCCAAAGAATTAG | 25831 |
rs145749647 | snp | C/T | 0.000616364 | 0.0175443 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119676 | TGATTTAGTATGTAT[C/T]AAAATTAAATCACAA | 25831 |
rs145754862 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189161 | CAAAAGCCATATTAC[G/T]CATATCCTCTAACCT | 25831 |
rs145765016 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131638 | CTGTTGTGCCATTGT[A/G]TCTTGGGAAAAAAAA | 25831 |
rs145770215 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200678 | TCCAGTTACTGGGGC[A/G]GCTGAGGCAGGAGAA | 25831 |
rs145837737 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145965 | TGGAACCCTTGCCAC[C/G]CTCACTCCACACCCT | 25831 |
rs145873829 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137044 | AGCCAGGATGGTCTT[G/T]ATCTCCTGACCTCGT | 25831 |
rs145875809 | snp | A/G | 0.040671 | 0.13668 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165975 | CTCACCCTCCCGAGT[A/G]GCTGGGACTACAGCC | 25831 |
rs145904671 | in-del | -/TAAATCTAATTTTATA | 0.00117747 | 0.0242353 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109372 | GTCATTCCTGTTCCC[-/TAAATCTAATTTTATA]TGAGATTACCTCAAG | 25831 |
rs145928338 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102721 | AGGTGTGAGCCACCG[C/T]GCCCGGCCTGCTGTC | 25831 |
rs145971813 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159529 | AGTTTTAGTAGAGAC[A/G]GAGTTTCATCATGTT | 25831 |
rs146012891 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194534 | TTACCTCTTACATTA[C/T]AGGTAGAAATTCTTC | 25831 |
rs146025898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192249 | AGGTAGGAGGACAAT[C/T]GCTTGAACCCAGGAC | 25831 |
rs146083197 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143815 | CATATTCTATTTTAT[A/G]TAACTTATGTAAAAA | 25831 |
rs146091460 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138263 | TAATAAACTTTAAAA[C/G]ATGCAAAATAGTTTT | 25831 |
rs146092777 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140174 | ATTTCCTTTACTTAA[A/G]AATAAAACATTTCAT | 25831 |
rs146104031 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209564 | GGAAGAAATCTAAAA[A/G]TAATTTTTGAAAGAA | 25831 |
rs146146726 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176874 | CCCAGGAGGCAGAGG[C/T]TGCAGTGAGCTGAGA | 25831 |
rs146213346 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121022 | GCACTTAGTTAGTGA[C/T]CATTAAGCGTTAGCT | 25831 |
rs146324459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179544 | AGTGCCTAGCATATT[A/C]AACTAAACTTTAGCC | 25831 |
rs146334511 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103463 | AGGAGAATGGCGTGA[A/G]TCCAGGAGGCGGAGC | 25831 |
rs146336386 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176510 | AAAGCTCTTTGGGTA[A/T]CCTCAATTATTTAAG | 25831 |
rs146410036 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201806 | TGAGCCACCGCACCC[A/G]GCCATGTTTACATTA | 25831 |
rs146438390 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132478 | TATACACACACATAT[A/G]TGTGGATATATATAT | 25831 |
rs146499944 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155463 | TAAACAGACACAAAT[A/G]TGCCTCCAAGAAGGA | 25831 |
rs146523384 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188378 | GTAGCTAGGATTACA[C/G]GCGCCTGCCACCACA | 25831 |
rs146568141 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121058 | AAACTACTACTGCTG[-/C]CATCTACTACCACTT | 25831 |
rs146618901 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135856 | AACCCCGTTTCTACT[A/G]AAAATACAAAAATTA | 25831 |
rs146629764 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132298 | CAAAATTAGCCAGGC[A/G]TGGTGGCCCATGCCT | 25831 |
rs146640217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174853 | ATAATTATAAACAGG[A/G]GAACACTAAAAAAAT | 25831 |
rs146651763 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169981 | TAAGTATATTCCATC[C/T]TAACATGTCACCTTC | 25831 |
rs146737356 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118615 | ATAACACAAACTTGC[C/G]AGGCACGGTGGCTCA | 25831 |
rs146750634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116547 | AACAAGGCTACATGA[A/C]ATCCAAACCTCTCTG | 25831 |
rs146763035 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157788 | CTAAAAATACAAAAA[C/T]TAGCTAGACGTGGTG | 25831 |
rs146771754 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150376 | CTTTTTCCCCCCTTT[C/T]AGAAACATGGTCTCA | 25831 |
rs146788164 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131810 | ACTTTTTAATAAGTA[-/T]CATCAAGATGCCTAA | 25831 |
rs146829214 | in-del | -/T | 0.0566069 | 0.158427 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181178 | CTGTACATCAAAAAA[-/T]AAAATAAAATTTAAG | 25831 |
rs146846664 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152310 | ATTTGGGATCATAGG[C/G]GTGAAGTTCCCTAGA | 25831 |
rs146846962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193433 | AGTACTATTTGTCTA[C/T]GTTTATATCAATACC | 25831 |
rs146860105 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101558 | AGCACCTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 25831 |
rs146862452 | snp | G/T | 0.000934642 | 0.0215974 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173651 | GCGACCTGGTTTGCA[G/T]GCTGATGATGGTCCT | 25831 |
rs146882347 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201077 | TTTTTTACCTTTTAG[-/A]TGTAAACATATCAAA | 25831 |
rs146884211 | snp | G/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208109 | CACAGCAAAGCTGCG[G/T]CCCAACCTGTCCCCG | 25831 |
rs146897224 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190423 | GATCAGGATGAACTC[A/C]CCGAGTCCAGATTGT | 25831 |
rs146982210 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137412 | TGGGATTACAGGCGT[A/G]AGACACCACGCCCAG | 25831 |
rs146992316 | snp | C/G/T | 0.00280783 | 0.037364 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133457 | AACCAAATCACTTTT[C/G/T]ACAAAAGTAATTGTT | 25831 |
rs146992357 | snp | C/T | 0.00297892 | 0.0384784 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178296 | CTAGGGTTATTAAAT[C/T]CTTAACAGCAAAATA | 25831 |
rs147088466 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126636 | AAAAAAAATGACATA[C/T]AAAGTTCCTAGATCT | 25831 |
rs147095526 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117762 | AATATTTAAAATTAC[C/G]AATGGCAACAACACT | 25831 |
rs147096944 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160898 | TGGTCTCAAACTCCT[C/G]GACTCAAGCAATCCT | 25831 |
rs147151322 | snp | G/T | 8.45988e-05 | 0.00650325 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149115 | GTAGATGGCTTTACT[G/T]GGCCTCGAGCTCTTT | 25831 |
rs147218947 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134647 | TTTGGCTAAGATACA[A/G]TGTAAAATAGCTCGG | 25831 |
rs147221635 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204160 | TCGATCGACATTTGG[A/G]TTGGTTCCAAGTCTT | 25831 |
rs147256969 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130674 | ATCCACACACCCAGA[C/T]GCTCACCCACACTTA | 25831 |
rs147258031 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200402 | TGTAATCCCAGCACT[C/T]TGGAAGGCCAAGGCG | 25831 |
rs147329004 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187862 | TCAAGCAATTCTCCT[A/G]CCTCAGCCTCCCAAG | 25831 |
rs147363023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114837 | AACAAAATGGTATAG[C/G]CTACTATCTACGTAG | 25831 |
rs147364051 | snp | A/C/G | 0.0150606 | 0.0854603 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185132 | CGGATCATGAGGTCA[A/C/G]GAGATCGAGACCATC | 25831 |
rs147424130 | snp | C/T | 6.62647e-05 | 0.00575569 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128688 | TAGATTCATGTTGTT[C/T]GTGGCATTAGTCCGT | 25831 |
rs147433385 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172341 | AGGCACCGTGGCTCA[C/T]GCCTGTAATCCCAGC | 25831 |
rs147433901 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125827 | ATCTTCACATAAACT[C/T]TGTCTTTAAAATTAC | 25831 |
rs147469482 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167779 | GTATCCTTTAAACCA[C/T]AATTTAAATCTCACC | 25831 |
rs147527156 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114600 | GATTAAGGTGTGTCA[C/T]GACACCCAGCCTCAA | 25831 |
rs147536833 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110543 | AATGGCATTAAATGG[A/T]ACAAAAATGTAACTA | 25831 |
rs147537455 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154324 | TTTTTTTGAGATGGA[A/G]TCTTGCTCTGTCGCC | 25831 |
rs147572688 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105879 | AGGACTTTTTAAATG[C/T]AATATTCTATGGACA | 25831 |
rs147593565 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141520 | TGCTTGAGCCCAGGA[C/G]GTTGAGGCTGCAGTG | 25831 |
rs147688327 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126180 | TGTATTGAGTGAAAA[C/G]AGCTGGCGGAAAAGG | 25831 |
rs147690260 | snp | C/T | 0.040671 | 0.13668 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196051 | CGGAGTCTCACTCTG[C/T]CTCCCAGGCTGGAGT | 25831 |
rs147698012 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122810 | TTTTTTATACTGGTG[C/T]CACATTTCCTTGCTT | 25831 |
rs147699818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193083 | GAAGTAAAAACCTTC[A/G]AACATAAAAATTTAT | 25831 |
rs147790221 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111396 | TAGCTGAGACTACAG[A/G]TGCCCACCACCACAC | 25831 |
rs147790655 | in-del | -/GTT | 0.00914312 | 0.0669923 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187750 | TTGTATGAACTCATG[-/GTT]TTTTGTTTTTCTTTG | 25831 |
rs147792925 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182108 | CATGTTGGCCAGGCT[C/G]ATCTAGAACTTCTGA | 25831 |
rs147803035 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177882 | AGTAAGACTGAAGAT[A/G]GGAAGAATTTTTTTT | 25831 |
rs147899135 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165167 | TCATAATACTGGTAT[C/T]TGAGGTACTTGAATC | 25831 |
rs147907650 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160760 | ACTGCAGCCTCGACC[A/G]CCCAGGCTCAAACAA | 25831 |
rs147917910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196679 | GCATTGCTTGAACCC[A/G]GGAGGCAGAGGTTAC | 25831 |
rs147929821 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199033 | AGAATCTGCCTCGAA[-/G]AAAAAAAAAAAAAAA | 25831 |
rs148023612 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167149 | TACACTCCAACTTGG[A/G]TGACAGAGCAAGACC | 25831 |
rs148056478 | snp | C/T | 5.06192e-05 | 0.00503061 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106636 | TGAAGAATGTACATA[C/T]AATGCTTACCCTAAA | 25831 |
rs148103308 | in-del | -/TTC | 0.00835141 | 0.0640778 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208441 | GTATGTCTGTGGTTA[-/TTC]TTTTCAAACTTTATT | 25831 |
rs148111289 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139439 | CATCTAAGAGGAATA[A/G]GCCCTCACGAGACAC | 25831 |
rs148120097 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152230 | AGACATTTGCATTCC[A/C]AACAGCCAGAGTAGA | 25831 |
rs148173576 | in-del | -/T | 0.245346 | 0.249957 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203751 | TTAACATGGCAACAC[-/T]TTTTTTTTTTATTAT | 25831 |
rs148174354 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158116 | TAAATGAAAATAAGA[G/T]ATCCTAATAATCCCA | 25831 |
rs148235966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128255 | AGAAGCTAAGATCAA[C/T]GTAGAGTCTAAACAA | 25831 |
rs148237068 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199804 | ACATAAACAAAAGTT[C/T]TTCAGGATCCACAAT | 25831 |
rs148269265 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142419 | GACTATGGGACTCAT[C/T]GAAGTTCCAGTGAAT | 25831 |
rs148324716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176407 | ATGTATAACATGTAA[C/T]TAATTTATTTTAAGA | 25831 |
rs148328834 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117743 | CAAAACGGGGTACAG[A/G]GCTAATATTTAAAAT | 25831 |
rs148382814 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120518 | CATAAGACCTCTCTG[A/G]AGTATTTTCGCAACC | 25831 |
rs148428520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114954 | TTGTGTATCTAAACA[C/T]AAAAAAGGTACAGTA | 25831 |
rs148438198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154958 | AGTCTAAGGCAAGAG[C/T]TACCAATGAATACAG | 25831 |
rs148491637 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159767 | GCCTCAGCCTCCCAA[A/G]TAGCTCGGACTACAG | 25831 |
rs148495393 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099698 | AACTGGAATTTGGAA[A/G]ATCTACTTTGGAATT | 25831 |
rs148551648 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131931 | TATGAATTTTAGGTC[A/G]CTGTAAACCTGTTTT | 25831 |
rs148554023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200775 | GACAGAGCAAGACTC[C/T]TGTCTTGAAAAAAAA | 25831 |
rs148577056 | in-del | -/T | 0.358303 | 0.225323 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206628 | TAAAAGTTAAAAAAA[-/T]AAAAAAATTAAAAAA | 25831 |
rs148584427 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145576 | CTCAGGAGACTGAGG[C/T]GGGACAATCATTTGA | 25831 |
rs148593926 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184796 | ATGCATATAGGTTAA[C/T]AGTATTTATTCACAA | 25831 |
rs148646167 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118294 | ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCTAATA | 25831 |
rs148697935 | snp | A/T | 0.0752113 | 0.178743 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122287 | GTGTGTGTGTGTGTG[A/T]GATTCTGTGGCTCAG | 25831 |
rs148771101 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181039 | GTTTTCTTTAGAAAA[C/T]AGTAGTTTTTTGAAT | 25831 |
rs148794215 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110141 | CCAGTAGCTGGGATT[A/G]CAGGTGTGTGCCACC | 25831 |
rs148815501 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102663 | TCAAACTCCTGACCT[C/T]AAGTGATCCGCCCGC | 25831 |
rs148816537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175206 | TCACAGAAACAATGC[A/G]CTCTCCAAATTTATT | 25831 |
rs148819637 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198400 | CATTTCAAGGAAAAC[A/G]ATCAACTGTATTTGT | 25831 |
rs148877735 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147183 | CTGGGCATGGTGGTA[C/T]GTGCTTGTAGTCCCA | 25831 |
rs148923530 | in-del | -/T | 0.0543475 | 0.155628 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181855 | ATACGTAAAATGCAC[-/T]TTTTTTTATATCAAG | 25831 |
rs148966847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189337 | TCTTTTTTGTATTAC[C/T]ACCACAGCTTCCTAA | 25831 |
rs149018277 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123875 | ATGGCCAGTAGAAGA[A/G]GCCTGCCATTATATT | 25831 |
rs149019332 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193971 | AAAGCTTATGTTCTC[A/G]CACACACACAAAATC | 25831 |
rs149025458 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137086 | CTTGGCCTCTCAAAG[C/T]GCTGGGATTACAGGC | 25831 |
rs149086764 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111780 | TGTGCTCAATATGCA[A/C]ATTAATTCTCTTGGT | 25831 |
rs149088728 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182571 | AAACTCACATTACTG[G/T]CCAGGCGCAATGGCT | 25831 |
rs149138779 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117320 | GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG | 25831 |
rs149176190 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157572 | ATTCTATATTCTACA[C/G]TTTACTAGCATGAAT | 25831 |
rs149184136 | in-del | -/TAA | 0.0014852 | 0.0272102 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144980 | GTGAATTTTTACAAT[-/TAA]TAATTTTACCAAATC | 25831 |
rs149230551 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161649 | CAGGCTGGGTGTGGT[A/G]GATCACGCCTGTAAT | 25831 |
rs149236883 | in-del | -/AA | 0.0637235 | 0.166737 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209069 | TCCTGTTAACGAAAC[-/AA]GAGGAAAAAGAGGAT | 25831 |
rs149259353 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191880 | CAGATGTGGTGGTGC[A/G]TGCCTGTAATCCCAG | 25831 |
rs149312860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194894 | GATTTCAGAAGATTG[A/G]CAAAGACATGAAAGA | 25831 |
rs149345215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139303 | CCCCAGTGCAGTGGT[A/G]TTGGATGGTGGAACT | 25831 |
rs149462312 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118211 | GGGATTTCACCATGT[C/T]GGTCAGGCTGGTCTT | 25831 |
rs149504529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171542 | ACTAGTTGAATAAAC[C/T]TGTAGTACAGGATAT | 25831 |
rs149556995 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103308 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 25831 |
rs149558029 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176155 | TAGCAAAAGCTCATA[A/G]TAATACTCTAACACT | 25831 |
rs149608356 | snp | C/G/T | 0.000579502 | 0.017013 | missense | HECTD1 | GRCh38.p7 | 14:31109432 | CTGCATGTATTTGCA[C/G/T]GACATTCTCAGCCCA | 25831 |
rs149618026 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148562 | AATTATATGTAAATA[A/C]ATATTTAAGAAAACA | 25831 |
rs149663654 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141063 | CTCCCGAGTAGCTGG[A/G]ATTAAAGACGCCCAC | 25831 |
rs149717100 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146447 | AAACATAGTGCTTAA[A/G]TGCTATCCAGTGTTT | 25831 |
rs149726688 | snp | A/G | 0.030278 | 0.119257 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185960 | ACCTTAAATGAGCAC[A/G]ATACCTAATAATTCT | 25831 |
rs149733179 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125813 | CACCTTAAAAATGTA[A/T]CTTCACATAAACTTT | 25831 |
rs149785279 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131158 | GGGAATGGCCATGTT[G/T]ATTAGGCAAAACTAA | 25831 |
rs149823147 | snp | A/G | 0.000333483 | 0.0129085 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173600 | CTGATTACTCAATTT[A/G]GAATCTGCAGTGGTG | 25831 |
rs149868028 | in-del | -/AAC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136024 | TCTGTCTCAAAACAA[-/AAC]AACAACAACAACAAA | 25831 |
rs149873359 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105146 | AGCTGGGATTACAGG[C/T]ATGCGCCACCATGCC | 25831 |
rs149876042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177120 | TTCCTAATCTTCAAA[G/T]TCCTAAACTTCAAGT | 25831 |
rs149928654 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111482 | TGGTCTCGATCTCCT[A/G]ACCTCATGATCTGCC | 25831 |
rs149934846 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121861 | GTATTTTTTAGGCAC[A/G]ATTTTCAGTTAGAAG | 25831 |
rs149938310 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149731 | AACAAGGTGAAACCC[C/T]ATCTCTACTAAAAAT | 25831 |
rs149945720 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164177 | ACTGATCTGCTGTCT[C/G]CCTTTTATTTCCTGA | 25831 |
rs149998757 | snp | C/G | 4.97211e-05 | 0.00498579 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168458 | CTCCTTTATTAACTG[C/G]ACACATCCAATCACC | 25831 |
rs150001073 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192963 | GCCTGGCGGCAGAGC[A/G]AGACTCCACCTCAAA | 25831 |
rs150034945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206327 | GCAAAGAACACCTAA[C/G]TAAAGGTTCTGTTTT | 25831 |
rs150105100 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132937 | TAAAGAAAAACATAA[C/G]AAATTAAAATAAAAC | 25831 |
rs150114730 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175677 | AAGACCAGCCTGACC[A/G]ACATGGAGAAAACCT | 25831 |
rs150168273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178777 | GTACTCCAGCCTGGG[A/C]AACGAGAGCAAAACA | 25831 |
rs150198525 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119536 | TAATTTGCTCCTTTA[A/G]AAAAACCTTTACTTT | 25831 |
rs150253044 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123429 | ATGACTACTTAAGAT[A/T]ATGCCTATTTACTAC | 25831 |
rs150261692 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165906 | GCTGGAATGCAGTGG[C/T]GCAATCTTGGCTCAC | 25831 |
rs150324452 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209227 | ATGTAGACACTGAAA[A/G]GAAAGGGAAGAACAT | 25831 |
rs150402030 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142622 | TGTTTTGTATTTTTA[A/G]TAGAGATAGGGTTTC | 25831 |
rs150410807 | snp | C/T | 0.00287817 | 0.0378259 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157204 | GATTTCCACTAGTAT[C/T]GTAGGCAAATTGTGA | 25831 |
rs150471341 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127038 | GTGCAGTGGTGCGAC[C/T]TCAGCTCACTGCAAC | 25831 |
rs150475067 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197057 | AGACGAGCTCGTAGT[C/T]CAGTGGAGAACTGAA | 25831 |
rs150478849 | in-del | -/GT/GTGT/GTGTGT | 0.231213 | 0.249293 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122263 | TTCATACACACACAC[-/GT/GTGT/GTGTGT]GTGTGTGTGTGTGTG | 25831 |
rs150480197 | in-del | -/A | 0.079617 | 0.182947 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137588 | TAAAACAAACAAACC[-/A]ACAAAAAATTAGCCA | 25831 |
rs150520677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190651 | TGGCACAATTACAGC[C/T]CACTGCAGCCTTAAA | 25831 |
rs150581533 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167584 | CTGCAGTGGTCAAAC[A/C]CTTTGGTAGTTTGGA | 25831 |
rs150631993 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31100023 | TTCTTTATGTAGTAA[C/T]TTCAGAAAACTTTGG | 25831 |
rs150665743 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112855 | CCTCTAACGATACAC[A/C]CACCTTGGCCCCCAA | 25831 |
rs150693998 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118156 | GATTACAGGCGCGCA[C/T]CACCAAGCCTGGCTA | 25831 |
rs150694535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145727 | ATATTTTGATGCATA[C/G]TTGTTTATATATGCA | 25831 |
rs150729089 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159123 | CAACTGATGTCCTAG[A/C]GAGGCATGTGACACA | 25831 |
rs150783106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163451 | CTTTCCTCCCCCAAA[A/G]AATTAGCTGGGCGTG | 25831 |
rs150791587 | in-del | -/GTT | 0.030665 | 0.119967 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160517 | GATTCAAAAAAGGTT[-/GTT]AACACCTTAAATTAT | 25831 |
rs150792911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200278 | GCCTCCTATCAAGTC[C/T]ACAAGCATTTGTTTG | 25831 |
rs150844249 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134766 | TTTTTAGAAAGAAAA[C/T]TTTGCTTCAATATTT | 25831 |
rs150846739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205534 | GAACCAACCAAGCTA[C/T]GGGTTAAAATTAATA | 25831 |
rs150898585 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140731 | ACAGTAATACTTCAA[A/T]ACATTATACATCCAT | 25831 |
rs150908911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181831 | AAGGTATCCGGGGCA[C/T]ATTCCTACATACGTA | 25831 |
rs150953697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175521 | CAGTGAGCCATTATC[A/G]CCCATTGCATTCCCA | 25831 |
rs150960369 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115251 | TGAAGGGCGGGAGAA[C/T]ACCGTTATGATTTTC | 25831 |
rs150962485 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185816 | ACTCTCAAATCCCTT[A/G]CCCCATTTCTGGCTA | 25831 |
rs151012046 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119273 | CCTGATTTTGGGGAG[A/C]AATTAGTATGCCTAC | 25831 |
rs151049575 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160249 | GCTAATAAATTACAG[A/C]GCCTGTATTCAAATT | 25831 |
rs151077083 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165745 | ATCTCCTTGCCTTTG[C/T]AGGAATATAGCAGTA | 25831 |
rs151107657 | in-del | -/A | 0.0532157 | 0.154195 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187410 | ATCTAAGCCAACTTC[-/A]AAAGTCTGGTTTGCA | 25831 |
rs151109651 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103864 | CCCAGCTACTCGGGA[A/G]GCTGAAGCAGGAAAA | 25831 |
rs151113822 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201119 | TACCACTGTGTTCAA[A/T]AACTTTGGAATCCAG | 25831 |
rs151164912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137224 | CAACCTCTGCCTCCC[A/G]GCTTCAAGCAATTCT | 25831 |
rs151167590 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208778 | TAATTACCCAGATGC[A/G]GTGACGCACACCTAT | 25831 |
rs151228458 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182672 | GCCTGGCCAACATGG[G/T]GAAGTCTCATCTCTA | 25831 |
rs151260411 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122487 | TCATACACGTGTGTA[C/T]GTGTGTGTGTGTTTG | 25831 |
rs151321412 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169835 | CAGTGAGCCAAGATC[A/G]CTTGAACCATTGCAC | 25831 |
rs180676092 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165551 | CTTTCACATGGCCTA[C/T]AAAAGCCATCATAGG | 25831 |
rs180676916 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192620 | AAAGGATAAAAGGGA[A/C]TATCACAAACAACTC | 25831 |
rs180682205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146124 | TATTCCAAAAAACTC[C/T]TGAGGTAGGTGATTT | 25831 |
rs180691228 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186573 | CGTGTCTGTTATCCC[A/C]GCTACTGGGGAGGCT | 25831 |
rs180697887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201835 | TACTACATTTTAGAA[C/T]TCGATACATCAGGTA | 25831 |
rs180906565 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129647 | TAGCTATCTGAAAGT[C/G]TATATTATTTAACTC | 25831 |
rs180921205 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168966 | GAAGAATGACGTAAA[A/C]CCGGGAGGCGGAGCT | 25831 |
rs180927876 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149448 | GTCTCCAAAACAAAA[A/G]AAAAAAAAAAAAAAG | 25831 |
rs180931088 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188620 | ACAGACCTGTTTTTT[A/T]CTCTTTAGAATTTAT | 25831 |
rs180935673 | snp | C/T | 0.000265406 | 0.0115166 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116415 | AGCTAATCGAGGTGA[C/T]GGAGTACATTCGACT | 25831 |
rs180947478 | snp | C/T | 0.030278 | 0.119257 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207693 | GCGGCGGCGGCGCGG[C/T]GGGGAGGCCCAGTCC | 25831 |
rs180953039 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159768 | CCTCAGCCTCCCAAA[C/G/T]AGCTCGGACTACAGG | 25831 |
rs180954982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199191 | ATCTGTGGATGATTT[C/T]TTCATATATTTCAAT | 25831 |
rs180956360 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104677 | CCTATGTCCACTTTC[A/T]TTCTTTCTTTGTTGA | 25831 |
rs180974978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141473 | GTTCATGCCTATAAT[A/C]CCAACACGTTGGGCA | 25831 |
rs180983849 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182618 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 25831 |
rs181093757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115356 | CAGAAAACATACTAA[C/T]AGAAGTGAAGTTACA | 25831 |
rs181103772 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139500 | CCCAGCCACCAGAAT[G/T]GTGAGCAATGAATTT | 25831 |
rs181216262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130284 | ATATTAAATAATTAA[A/G]TTCAATAAATTTGAA | 25831 |
rs181238758 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188994 | ATTTCCCATAGTAAA[C/G]CAAAATGTCAACTCT | 25831 |
rs181244840 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169896 | TCTCAAAAAACAATA[C/T]AAAGCAGCCTATCGT | 25831 |
rs181262369 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208990 | ATTTTGGAAATGACA[A/G]ATTTGTACTTCAGAT | 25831 |
rs181364128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151844 | TAAACAACTAAAATA[C/T]AGACAAGATATACGA | 25831 |
rs181371997 | snp | A/C | 0.107341 | 0.205301 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181632 | AAGAAAAAAAAAAAA[A/C]AACAACAACAAAAAA | 25831 |
rs181376527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131350 | CATAGGGAGGTGCCA[C/T]ACCTCACGGTTCAAA | 25831 |
rs181378099 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170151 | GTGTGGTAGCTCACG[C/G]CTATAATCCCAGCAC | 25831 |
rs181380902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198329 | TCAGACAAACTGATC[A/T]TTCAGACTTGGCTAT | 25831 |
rs181421126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122597 | TTTTTACCTCAGCCT[A/C]CCAAGTAGCCAGGAC | 25831 |
rs181431907 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31100067 | ACAAGTACCTGCTAA[A/G]GCTCTTAAGTCTGAT | 25831 |
rs181455335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135375 | TCAAAATTCCTTAAA[A/C]CACAGAATATTCAGA | 25831 |
rs181465090 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175871 | CTCTGTCTCAAAAAA[A/T]AAAAATAATAATAAT | 25831 |
rs181562440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112017 | AAAACAAAAAAACAG[C/T]AATGCCAACAGCCTG | 25831 |
rs181575113 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112299 | TGCTGACTATTCTTT[A/G]TAAGAATACAAGATA | 25831 |
rs181584196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155326 | CTCCAGCCTCAGCAA[C/T]AGAGCAAGATACCGT | 25831 |
rs181585892 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137034 | TCACCTTGTTAGCCA[A/G]GATGGTCTTGATCTC | 25831 |
rs181598015 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155605 | ATTAACTGTTCTATT[C/G]TCTTCATAAACACCA | 25831 |
rs181600823 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192908 | CTTGAACCCAGGAGG[A/C]GGAGGTTGCAGTGAG | 25831 |
rs181631972 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189591 | CATAGCGAGATCCCA[C/T]CTCTACAAAAATTTT | 25831 |
rs181818239 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203228 | TTCCATCTCACTATG[C/G]CTCCCTCACTAGTTT | 25831 |
rs181841650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193664 | CGTGGTAGCTCACGC[C/T]TGTAATCCCAGCACT | 25831 |
rs181843277 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177335 | AACACAGTGAAACTC[C/T]ATCTCTACTAAAAAT | 25831 |
rs181870076 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121186 | TAAACTCCTGCATGC[A/G]TTATGTCACAGCAAT | 25831 |
rs182012369 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145849 | CTTTTATTTTAGATT[C/T]GGGGTACATGTGCAG | 25831 |
rs182037760 | snp | A/G | 6.6855e-05 | 0.00578126 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112548 | GCCAATGGTTCCTGC[A/G]AATTAACAAATAATA | 25831 |
rs182037956 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156026 | GCAGAGGCGGGCGGA[A/T]CACGAGGTCAGGAGA | 25831 |
rs182043878 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185838 | TTCTGGCTAAATGAA[C/T]GACCCCCCACATTCC | 25831 |
rs182071948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187297 | CTGGAGGTGGAAGGG[A/G]CAGTGAGCCAAGATC | 25831 |
rs182074367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167230 | CAGCACTTGGGAGGC[C/T]GAGGTGGGCGATCAC | 25831 |
rs182079307 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147831 | ATTACAATTTCTCTG[A/G]TCAAAGCCATAAAAA | 25831 |
rs182084347 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188067 | GGCCTGAACACATGG[A/G]TTTCAAAATATAGAG | 25831 |
rs182102386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204317 | AGATCCTTGAGGAAT[C/T]GCCACACTGTTTTCC | 25831 |
rs182271666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118218 | CACCATGTCGGTCAG[A/G]CTGGTCTTGAACTCC | 25831 |
rs182276117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152883 | TCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 25831 |
rs182284538 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143904 | GCAAATTATAACTGG[A/G]AACTTAGAAATCAAA | 25831 |
rs182284596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190786 | CTTGGCCTCCCAAGT[A/G]TGGGGAGTCGCTGCG | 25831 |
rs182289408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170610 | TCACTCAGTATTAGT[A/C]ACCCTTAGAAGCATC | 25831 |
rs182309874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137292 | CGTGCCACCACGCCC[A/G]GCTACTTTTTGTATT | 25831 |
rs182317183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164336 | TTGTAACCAATCCAC[C/G]TTGTTTTTTCGAGAC | 25831 |
rs182325359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201442 | TAACATTAATACATA[G/T]GATGATCACCTATTT | 25831 |
rs182357675 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102635 | AGGTTTCACCGTGTT[A/G/T]GCCAGGCTGGTCTCA | 25831 |
rs182368318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137516 | GAGGATCAATTGCTT[A/G]TGCCTAGGAGTTCAA | 25831 |
rs182373609 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178659 | ATGCAAAAAATCAGC[C/T]GGGCGTGGTGACAGG | 25831 |
rs182592648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159344 | TAATTTAATTTAATT[A/T]ATTTATTTTTTTTGG | 25831 |
rs182594311 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115767 | CAGAGAGAGACCTTG[C/T]CTCAGAAAAAAAGAA | 25831 |
rs182609410 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117316 | AGTGGAGGTTGCAGT[A/G]AGCCGAGATCACACC | 25831 |
rs182617985 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156492 | CCTGGACAACAAGAG[C/T]GAAACTCCATCTCAA | 25831 |
rs182628505 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112829 | TGGCCAGGCTGGTCT[C/T]GAACTCCTAGCCTCT | 25831 |
rs182634591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160216 | GCGATAGTTAAGTCA[A/G]TCTACTAAGATCACC | 25831 |
rs182651565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126156 | ACATATGTGAAAATA[C/T]TTTCACAATGTATTG | 25831 |
rs182652677 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199584 | GCTGGACACGGTGGC[A/G]CACACCTGTAATCCC | 25831 |
rs182653872 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182756 | CTTGAGAGGCTGAGG[C/G]AGAAGAATGGCATGA | 25831 |
rs182657705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194817 | GAAAGAATTTCCCTG[A/G]GAACTGTAATATTTT | 25831 |
rs182664368 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132067 | TGAATAAATAAATGT[A/C]TTTACCACATAAAAC | 25831 |
rs182690803 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161329 | CACGCCTGTAATCCC[A/G]CAGTTTGGGAGGTCA | 25831 |
rs182697125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200689 | GGGCGGCTGAGGCAG[A/G]AGAATCACTTGAACC | 25831 |
rs182909947 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200314 | TTCCCACTTCCTATC[C/T]CTCCTTACTCATCCT | 25831 |
rs182910325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108059 | CAGACTTTTGTGTGT[C/G]TCTGTGTGACACCAA | 25831 |
rs182961567 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153249 | TACAAAAAATTAGCC[A/G]GGCATTGTGGCGGGC | 25831 |
rs182962959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108837 | TTCACCCCTGTGACA[C/G]GAGACGTATTTCCAC | 25831 |
rs182984448 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184456 | AGCCAGGCATGGAGG[C/T]GTGCACCTGTGGTCC | 25831 |
rs182992888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191602 | TATAACATCAAACTT[C/T]GTAGGATACAACTAA | 25831 |
rs183113849 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137952 | CTTATAAAACTTCTT[A/C]ATCAAAGTGACTTAT | 25831 |
rs183119059 | snp | A/T | 1.65655e-05 | 0.00287793 | missense | HECTD1 | GRCh38.p7 | 14:31113316 | GGTCACTTGCAACTA[A/T]ATATAGAATACGCAG | 25831 |
rs183125145 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157607 | ACATGTCATGATAAT[A/T]TTAGAAAATCAAGTA | 25831 |
rs183135035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195079 | ACATCTTTTGATCCA[C/T]TTCATATTCCATTTT | 25831 |
rs183140970 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179018 | ATATTTTTCAGAAAG[A/C]AGCACTGATTTGGGG | 25831 |
rs183176176 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101869 | AATACTGACAGTGTA[C/T]GGGGTCCATCTATTC | 25831 |
rs183193253 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147300 | GTCTGGGTGACAGAG[G/T]GAGAATCCATCTCAA | 25831 |
rs183205536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124615 | ACAGTAGACACTAGC[A/G]ACTCCAAAAGGAGTG | 25831 |
rs183212427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166633 | AGGCCAGAGGATTGC[A/T]TGAGCCCTGGAGTTA | 25831 |
rs183253218 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133162 | GTGCTCATACATTTA[G/T]GCAATTTATAAATTA | 25831 |
rs183255614 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143170 | CTGTAATCCCAGCAC[C/T]TGGGAGGCAAAGGCG | 25831 |
rs183259688 | snp | C/T | 0.000166044 | 0.00911013 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172151 | GGAAAAAAAAAGAAA[C/T]GTATTTTTAAAGCCA | 25831 |
rs183259845 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183164 | CAGTATGTGAAAACA[C/T]ATACATTAAAAAAAA | 25831 |
rs183374767 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195429 | CAAAGCGTTATAAAA[C/G]ACAATGTCATACCCA | 25831 |
rs183440070 | snp | A/G | 0.000199657 | 0.00998943 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107170 | TTCAAGCTCATCACT[A/G]TCCTGTGGAAATGGT | 25831 |
rs183470551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117664 | ATATCCCAGTTACTG[A/G]ACATAATTAAGGTCA | 25831 |
rs183482903 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115227 | CTTGGGAACTTGGGG[A/G]AAAAAAACTGAAGGG | 25831 |
rs183489102 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160579 | TTTTACTTAAAAAAA[A/T]TTCTCATTTTTTAAG | 25831 |
rs183494404 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123335 | CAACATGTAAAAGAT[C/G]TTACGAGGAAAAACA | 25831 |
rs183504305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139249 | TTGCCATGGTCTGAA[C/T]GTTTGTGTCCCCGCA | 25831 |
rs183535115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165777 | ATAAGACCAGCTCTC[A/G]TGGTGCTTACTTTAA | 25831 |
rs183684576 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188659 | TCTTCTTATCCATTG[C/T]AACTCTCTCCTAAAA | 25831 |
rs183690809 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169153 | TTTTGGTTATTCTGG[A/C]ATCAGGCAGTCACAA | 25831 |
rs183704818 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207786 | GGGCAGCCGAGCCCG[A/G]CGGAGGCGGAGCAAA | 25831 |
rs183727066 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101598 | AAGAGTTCAACAGCA[A/G]CCTGACAAACATGGT | 25831 |
rs183752840 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146711 | TGCAAAAATGAGCCG[G/T]GCATGGTGGCGCGCA | 25831 |
rs183844355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157844 | CAGGAGCCTGAGGCG[C/G]AATAATCACTTGAAC | 25831 |
rs183845270 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187670 | ACTGAAGGAAAAGAG[A/T]ACTGAAAATACAGAA | 25831 |
rs183922579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192418 | CAGAAAGCAATAATA[A/G]AGAACAGAAATCAAT | 25831 |
rs183929857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175501 | AGCCCAGGAGGTCAA[C/G]GCTGCAGTGAGCCAT | 25831 |
rs183969464 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144800 | TAAAATCTAGAGGAT[A/G]ACATACTTGTCTATT | 25831 |
rs183975794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112080 | CACGGTAACACTTGT[A/G]GGGCATTCCTTTTTG | 25831 |
rs183981403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119183 | GATTATCTCCCCTTC[C/T]CAAGATCCCTAATTA | 25831 |
rs183981738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162965 | AGTATCAGCAACTTG[A/G]GAGGCTAGAGAACTG | 25831 |
rs183994318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185034 | CATTGTAATTTAAAC[A/C]GATAAGATTTAAAAA | 25831 |
rs184001700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200716 | AACCTGGGAGGTGGA[A/G]GTTGCAGTGAGCTCA | 25831 |
rs184030540 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203436 | GTATCTTCATATAGT[A/G]AATCATATCTGACTT | 25831 |
rs184049546 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179904 | TATGAGGCCAGGCCC[A/G]GTGGCTCACGCCTGT | 25831 |
rs184172490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181067 | AATAAAGAATAAAAT[A/G]AAGTTGATAGTCCAA | 25831 |
rs184194411 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149672 | CGTTGGGAGGCCGAG[G/T]TAGGGGGATCACCTG | 25831 |
rs184321684 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158349 | CAACCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 25831 |
rs184328379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197107 | AGTGTATACATGTGA[A/G]AATATGCAGGAGGGG | 25831 |
rs184384324 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134221 | CTCCTCTCATACCAT[A/G]TCAAATGCCAAAAGC | 25831 |
rs184387312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110352 | GTGGGAGGAAGAACC[A/G]ACAATTAGGAATAAG | 25831 |
rs184391224 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174469 | ACAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTC | 25831 |
rs184400411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153788 | ACATGGGTAGTAAGG[A/G]TTGAGACTAAGGGAG | 25831 |
rs184403660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192068 | TGTGGTGGCTCACGT[A/G]TGTAATCCCAGCACT | 25831 |
rs184449089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140198 | ATTTCATTTTTCTAA[A/T]AAAAACTTAATTATA | 25831 |
rs184459752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115380 | AGTTACAGTAAGAAT[A/G]ATGATATAATTTATT | 25831 |
rs184462246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159151 | ACAGCTGTATTTCTA[C/T]AGCATAGGGTCTCTA | 25831 |
rs184466360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134408 | TTCTATAACGAGCAA[C/T]AGCCACTGCTAATAT | 25831 |
rs184471289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197559 | GACCAACTGAATCAG[A/C]ATATGCATTTTAACA | 25831 |
rs184472516 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181281 | CCTGCTGTGTTCCCT[A/G]AAATGCGATGCATTT | 25831 |
rs184517508 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201685 | CAGCTAAATTTTGTA[C/T]TTTTAGTTGAGATGG | 25831 |
rs184582393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111456 | ATGGGGTTTCACCAC[A/G]TTAGCCAGGATGGTC | 25831 |
rs184611145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154904 | GAAATAAATCTTGCT[A/G]GGAACCACTAGACAC | 25831 |
rs184773533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155439 | TCCAAGTTATCATAA[C/T]CAACAGGGTAAACAG | 25831 |
rs184807633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192804 | AACATGGTGAAATTC[C/T]GTTTCTACTAAAAAC | 25831 |
rs184893819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136257 | TCAAATTAATAGAAA[C/T]AATTATCACACACAT | 25831 |
rs184895361 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128426 | AGGTTCTTTATCACA[C/T]CTAGTCTGAATTCTG | 25831 |
rs184902274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176000 | TCTTTAAAAATGCAT[A/G]TATACTTTATACTTA | 25831 |
rs184903940 | snp | A/G | 4.97748e-05 | 0.00498848 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148807 | CTGAACCTTGGGGGG[A/G]AAAAAAAGAATATTC | 25831 |
rs184910899 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104387 | TTGAATAAACAAGCA[C/T]AAATTAAGACAGCTT | 25831 |
rs184919205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168158 | AAAAGATAGGGCTTT[C/T]CCACTTCTCATCTAA | 25831 |
rs184937850 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188425 | ATTTTTAGTAGAGAC[A/G]AGGTTTCACCATATT | 25831 |
rs185043226 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145491 | GGCCAACATGGTGAA[A/T]CCTCGTCTCTACTAA | 25831 |
rs185053187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185645 | GATGGGAAGATCACA[A/T]GAGCCCAGGGAGGTC | 25831 |
rs185152828 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121101 | AAACTACAAATCTTA[C/G]ATACCATATATTAAC | 25831 |
rs185167570 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163481 | GGTGGTGCACAACTG[G/T]GGTCGCAAGTGGTTG | 25831 |
rs185207390 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141689 | TTTTATTCCATTAGA[G/T]TAAAAAAAACTTCAA | 25831 |
rs185213681 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116820 | ATTTTTAGTAGAGAC[A/G]GCAGGTTTCACCATG | 25831 |
rs185222271 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160018 | TTAGTTTTATATCAT[G/T]ACTTATTTCAATTAA | 25831 |
rs185264412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194313 | ATGTTCTGCATTTCA[A/G]TTATAGTGGTGGTTA | 25831 |
rs185292367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127240 | TTGGCCTCCCAAAGT[C/G]CTAGGATTATAGGTG | 25831 |
rs185299602 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167872 | GAGAACCCTGAATAT[A/G]TGCCTAATCTACCAT | 25831 |
rs185307822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205434 | TCATCTCTTATTCCA[C/T]AAATCAATTTCATGG | 25831 |
rs185397260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103413 | CGGGCGTGGTGGCGG[C/T]TGCCTGTAGTCCCAG | 25831 |
rs185403636 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148090 | AATAAACATACTAGT[C/T]ACCAGAAAATGTTGA | 25831 |
rs185415497 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188122 | AGATAGATAGATAGA[C/T]AGATAGATAGATAGA | 25831 |
rs185437379 | snp | A/T | 0.000116058 | 0.0076168 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121482 | GGAGCCAGCTCGACG[A/T]TGCAGGGATGGGCGT | 25831 |
rs185450308 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145983 | CACTCCACACCCTCC[A/G]TAATTTTTTTTTTTT | 25831 |
rs185468667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164608 | GACGAGCCAATTGAT[G/T]AAGAGGTTATGTGCT | 25831 |
rs185509389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114603 | TAAGGTGTGTCACGA[C/T]ACCCAGCCTCAAGGA | 25831 |
rs185514514 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199589 | ACACGGTGGCGCACA[C/T]CTGTAATCCCAGCTA | 25831 |
rs185719208 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207078 | CGTGCCCGAGAGGAG[A/G]CCGCCGGGCCAGGCA | 25831 |
rs185728379 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165603 | TTTCTTAACATTATT[C/T]TCGGAGCTTTCCAAA | 25831 |
rs185730038 | snp | C/G | 0.000217168 | 0.0104181 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112407 | AAACATAAAAAAAAG[C/G]CTTCTTACCTTGAGG | 25831 |
rs185737156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146204 | AAAATTTGTAACCTC[A/G]AAATCAATCATTGCA | 25831 |
rs185748527 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137065 | CTGACCTCGTGATCC[A/G]CCCTTCTTGGCCTCT | 25831 |
rs185760877 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202114 | ACACAGTGAAACCTC[A/G]TTTCTACTAAAAATA | 25831 |
rs185763381 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155702 | CTCAGGAATATGATA[A/T]GCAATGTAATGTGTG | 25831 |
rs185769489 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193234 | TCTATGATTCATCTG[A/G]GTTTTTAAAAATATA | 25831 |
rs185778360 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176665 | GGGCCAGTCACAGTG[A/T]CTCAAGCCTGTAATC | 25831 |
rs185827992 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104857 | TTTTAAAAAATGTTT[G/T]GTAGAGATGGGGTCT | 25831 |
rs185858033 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182623 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACTTGAG | 25831 |
rs185942440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130207 | AGTCACTAGTTCAAA[C/T]AAAACACTAAAGTTA | 25831 |
rs185991846 | snp | C/T | 0.000248729 | 0.0111491 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31106672 | TATGCTAAGTGGAGG[C/T]CCAGAACCTGATGGA | 25831 |
rs185999383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199220 | ATCAAAATAACATAA[C/T]GCAACAAACTGAATG | 25831 |
rs186102453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137421 | AGGCGTGAGACACCA[C/T]GCCCAGCCTATTAAA | 25831 |
rs186136101 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177729 | CTACCAGGAACTGAA[A/G]TGCACTGAAGCAGCA | 25831 |
rs186250599 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112634 | TTTTTTTTTGAGACA[C/G]AGTCTCACTCTGTTG | 25831 |
rs186252877 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156121 | GCATGGTGGCAGGCG[C/T]CTGCAGTCCCAGCTA | 25831 |
rs186253798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142882 | GAGCCCAGCCTAGGC[A/G]TCATGGCGAACACAC | 25831 |
rs186254915 | snp | A/C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185841 | TGGCTAAATGAACGA[A/C/T]CCCCCACATTCCCTA | 25831 |
rs186265159 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31107861 | AGCACAGAAGTGTTA[C/T]TTTAATTTTCCTAAA | 25831 |
rs186269681 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160337 | CTATTATATAAATTT[G/T]GAACATTTAGTTTAC | 25831 |
rs186284715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182950 | CAGCTGGATTAGGCA[A/G]ACTCCTTTCATTTAC | 25831 |
rs186298215 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170312 | GCACACGCCTATAGT[C/T]CTATAGTGACTCCGG | 25831 |
rs186303827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132000 | AATACATTTGGCAGT[A/G]AAATAATTCAAGGAA | 25831 |
rs186310187 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151946 | AGCGAGTCTCTTAGA[A/G]CCAGAGACCATTTTC | 25831 |
rs186313400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190223 | TGAGGTCCCAGATAT[C/T]GCAGAACAGAGACAA | 25831 |
rs186354065 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122759 | GTGGAGAATCATAAA[A/T]GCTCAGATTAAAACT | 25831 |
rs186441612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194990 | GTAAATCAGGCACTT[C/T]ATTTTAAAAAAATGA | 25831 |
rs186579076 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100817 | AAGCCTTAATGGTGG[A/G]AAAAAAGGCAAGTGT | 25831 |
rs186601313 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144458 | CAGTTTAGGCTTTGC[A/C/G]GGCCATATAGTCTAC | 25831 |
rs186607135 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118368 | AATCTTTGTTAAGGA[C/T]AATTTACTGATTATA | 25831 |
rs186612443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161476 | ACTCAAGAGGCTGAG[A/G]CAAGAGGATACACTG | 25831 |
rs186615565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178780 | CTCCAGCCTGGGCAA[C/T]GAGAGCAAAACAAAC | 25831 |
rs186618575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184550 | CCAAGATCACGCCAC[C/T]GCACTCTAGCCTGGG | 25831 |
rs186619198 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101661 | GCTGGGCGTGGTGGC[A/G]CACGCCTGTAATCCC | 25831 |
rs186651487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147034 | TAACTACTGTTGGCC[A/G]GATGTGGTGGCTCAT | 25831 |
rs186669517 | snp | A/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187546 | TACAGCATGAGCAAA[A/G]TGAACAGGACATTTG | 25831 |
rs186794599 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102425 | CCATGATGTCAGTTG[C/T]CTTTTTTTTTTTTTT | 25831 |
rs186808080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147685 | ATAGCCTGAACCCAG[A/G]AGGCAGAGGTTACAG | 25831 |
rs186822532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124658 | AGGGCTGAAAACTTC[C/T]TATTGGGTACTATGT | 25831 |
rs186823605 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166982 | GTTCAAGACCAGCCT[A/G]GGCAACAGAGCAACA | 25831 |
rs186855357 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123339 | ATGTAAAAGATCTTA[C/G/T]GAGGAAAAACAGAAT | 25831 |
rs186888331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165782 | ACCAGCTCTCGTGGT[A/G]CTTACTTTAAAGAGA | 25831 |
rs186891662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203312 | GAATGAAAAGCAAAC[C/T]AATGTTTAAAAACAA | 25831 |
rs186941700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130394 | ATGTACAGAATTAAC[A/G]AGCATAATGATATTC | 25831 |
rs186949696 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169904 | AACAATACAAAGCAG[C/T]CTATCGTAACTTGAA | 25831 |
rs186958984 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209277 | GACATAGGAAAGGTC[A/G]CCTGTGCCCCCAGCA | 25831 |
rs187081999 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188113 | TAGATAGATAGATAG[A/G]TAGATAGATAGATAG | 25831 |
rs187089807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167275 | TTGAGACCAGCCTGG[A/G]CAACGTGGTGCATCC | 25831 |
rs187101062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204594 | ATCTATGAACGCAAT[C/T]TTTAACTTGAGAGTC | 25831 |
rs187128618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150978 | GTGCGCACCTGTAGT[C/T]CTAGCTACTGGAGAA | 25831 |
rs187155268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189000 | CATAGTAAAGCAAAA[C/T]GTCAACTCTAGCCTC | 25831 |
rs187193484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159593 | GATCTGCCTGCCTCA[A/G]CCTCCAAAGCGCTGG | 25831 |
rs187196208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116010 | AAGAATTCAAATGAC[A/G]CTCTTTTCAACAATT | 25831 |
rs187210895 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137646 | TGGAGAGGCTAAGGC[A/G]GGAGGATCAGCTGAG | 25831 |
rs187211272 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113023 | GGGAAAGATGGTGAG[A/C]GGTAGAAAAGAAAGT | 25831 |
rs187229682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198442 | ACACTCAACTTTACA[A/G]GCAAAAATGACATTT | 25831 |
rs187378507 | snp | C/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208110 | ACAGCAAAGCTGCGG[C/G]CCAACCTGTCCCCGC | 25831 |
rs187415479 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141161 | TCGAACTCCTGACCT[C/G]AAGTGATCCACCCAC | 25831 |
rs187434789 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31113386 | ATTGCCTGCTTTGGC[C/T]TGAGGTTGTTCTTTT | 25831 |
rs187448683 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138020 | TAATTAGCTTACTCC[A/G]CTAGAATATATTCTA | 25831 |
rs187462221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157766 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 25831 |
rs187471579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195230 | ATGTAAGTTTGCTTT[C/T]CTCCAATTAAAATAC | 25831 |
rs187471865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179205 | AGGCAGATCACTTGA[A/G]GTCAGGAGTTCAAGA | 25831 |
rs187529633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108064 | TTTTGTGTGTCTCTG[C/T]GTGACACCAAAGCCT | 25831 |
rs187533875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153120 | TGGGTCGGCCAGGCG[C/T]GGTGGCTCATGCCTG | 25831 |
rs187547326 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187696 | CAGAAAGAGAAAACT[A/G]GCATGAGCCCTGTGG | 25831 |
rs187649044 | snp | C/T | 0.00366256 | 0.0426364 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156821 | TCTTCCTGATACCTC[C/T]ATAATTAAGACCACT | 25831 |
rs187676308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110094 | GCAACCTCCCTATCC[C/T]GGGTTCAAGTGATTC | 25831 |
rs187681175 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134102 | TTATGATGGAAAAAC[A/G]GACTTAAAAACATTT | 25831 |
rs187788463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173063 | GGTGCCACTTTGTTA[C/T]CTGGATTTCTAAGAG | 25831 |
rs187790171 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132159 | TGTGGTGTAAGTTGC[C/T]GCGTGCGGTGGCTCA | 25831 |
rs187804377 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170722 | ACCTGTTATTGAAAA[G/T]GTTGTTGTAGTGTAA | 25831 |
rs187821212 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200696 | TGAGGCAGGAGAATC[A/C]CTTGAACCTGGGAGG | 25831 |
rs187960384 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134274 | CCTGATATGTGCCAA[A/C]ATGCATAAATAAAAT | 25831 |
rs187968268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111023 | GTAGTACAAATATTT[C/T]GTAAATAATATCTGA | 25831 |
rs187976976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154083 | GCTGCTCCTTTTCCA[A/G]GTTGCTTTGGCTATT | 25831 |
rs187981265 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192162 | ATCAGCCTGGACAAG[C/G/T]TGGTGAAATCCCATC | 25831 |
rs188039130 | snp | A/C | 0.000958576 | 0.0218716 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157025 | CCTGAAAAATAAAAA[A/C]TAAAAATAAGTTTAG | 25831 |
rs188044280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114677 | GTAGCAGAAACCATA[C/T]TCCTGAATTATGATT | 25831 |
rs188049335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126561 | CTTCTTCTCTTAGTG[A/G]TAAGAGTGTCAAATA | 25831 |
rs188088309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191924 | TGAGGTAGGAGAATC[A/G]ATTGAACTCGGGAGG | 25831 |
rs188240396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122488 | CATACACGTGTGTAC[A/G]TGTGTGTGTGTTTGT | 25831 |
rs188250588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146039 | TGTCCTCACTGATTT[C/T]TTTTAGTTTGTGTTA | 25831 |
rs188254598 | snp | A/T | 0.00119737 | 0.0244387 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099690 | ATGGTAATAACTGGA[A/T]TTTGGAAAATCTACT | 25831 |
rs188266620 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165490 | TGTCAAATTTTCCTT[A/G]CAGGTCTTTAATAAT | 25831 |
rs188279272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201819 | CCGGCCATGTTTACA[C/T]TACTACATTTTAGAA | 25831 |
rs188286658 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186060 | TTTCCACTCTAGCTT[C/T]CTTCCTAGATTCCCT | 25831 |
rs188332934 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147931 | AGAACCAGGCATAGC[A/G]CCTGTAGTCCCAGCT | 25831 |
rs188350557 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188127 | GATAGATAGATAGAT[A/G]GATAGATAGATAGAT | 25831 |
rs188358529 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112184 | ACTCCATGTTTTCTA[A/G]AAGACCTAGAAAACA | 25831 |
rs188362434 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163119 | CGCACACACACACAC[A/G]GAAAGCAAGAAAAGA | 25831 |
rs188377285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185081 | GGCGCGGTGGCTCAC[A/G]CCTGTAATACCAGCA | 25831 |
rs188383266 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136744 | ATGATATACCCTAAA[A/G]CAACTGAGATTTGGA | 25831 |
rs188395452 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200924 | TGTAACCACATTTTT[C/T]CCCCACAATTATCTG | 25831 |
rs188397555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155535 | CTTTTGCTAAAACAC[A/G]TAAGCTGAATTTAAT | 25831 |
rs188587985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138547 | ATCCACTTACCAGGA[A/G]TAAAGCTTAAAAACA | 25831 |
rs188592085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180321 | CACTTGCAGTCTCAG[C/T]ACTTTGGGAGGCTGA | 25831 |
rs188597855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203883 | AGGTATATCTCCTAA[C/T]GCTATCCCTCCCCCC | 25831 |
rs188603803 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115337 | AGTGATGTTAAGAGA[A/G]CATCAGAAAACATAC | 25831 |
rs188618839 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167923 | CACATACATCCTTAC[C/T]AGCCCGCAAGGGGAA | 25831 |
rs188625870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139438 | CCATCTAAGAGGAAT[A/G]GGCCCTCACGAGACA | 25831 |
rs188627092 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206088 | AGCAATTAAAAAAGA[C/G/T]TCCTAAGTACGTTTG | 25831 |
rs188641947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158496 | TGATCTCCTGACCTC[A/G]TGATCCGCCTGCCTC | 25831 |
rs188791816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188877 | CATCCCTCCATACAC[A/G]ACTTCATCCTGGCCC | 25831 |
rs188799982 | snp | A/C | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208988 | GTATTTTGGAAATGA[A/C]AAATTTGTACTTCAG | 25831 |
rs188808928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117841 | GTGCCTATTTATACT[C/T]TCTAGAATGTGTTTT | 25831 |
rs188845610 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153413 | TCACCTCACCATGTT[A/G]CCCAGACTGGTCTCG | 25831 |
rs188849469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160829 | GTATGCGCCACCATA[C/G]TCAGCTAATTTTTGT | 25831 |
rs188857336 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158051 | AATTTTGATTTAATT[C/T]GTCCTTCATCAAATT | 25831 |
rs188890876 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140284 | TTTGATAAATAAAAA[A/C]GAATATAAAGCAACA | 25831 |
rs188891811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196128 | AAGCGATTCTCGTGC[C/T]TCAGCCTCCTGAGAA | 25831 |
rs188907261 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159205 | TGAAGTTATAACATT[A/G]TATTTCTTTAATGAA | 25831 |
rs188923975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181576 | GCCATGATCGCACCT[A/G]TGCACTCCAGCCTGG | 25831 |
rs188931677 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198232 | ATAAAGCACTGCATA[A/C]GGAAGAATAATGGCA | 25831 |
rs189016258 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103881 | CTGAAGCAGGAAAAT[C/T]GCCTGAACCCAGGAG | 25831 |
rs189102753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111726 | GATCATTTTCCTTCA[C/T]GTGTTTCAGGAAGCT | 25831 |
rs189112126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143211 | TTGAGGTCAGGAGTG[C/T]GAAACCAGCCTGGCC | 25831 |
rs189116353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183187 | AAAAAAAATAAATTA[C/T]ATAGAATTTGTTATA | 25831 |
rs189126780 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155277 | TTTAACCCAGAAGGT[A/G]GAGGGGGCGGTGAGC | 25831 |
rs189155532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192470 | GGGAAAATGAATGAA[A/G]CCAAAAGCTGGTTCT | 25831 |
rs189274617 | snp | C/T | 0.000529836 | 0.0162677 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129297 | CAAGCTGCTCCATGA[C/T]TGCGTTGTGCCTGAA | 25831 |
rs189288974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104481 | GAACATTCAGTTGCT[A/G]TGGTCAGTATGCAAA | 25831 |
rs189294938 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168960 | GAGGCAGAAGAATGA[C/T]GTAAACCCGGGAGGC | 25831 |
rs189316777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188514 | ACTGGGATTACAGGC[A/G]TGAGAAACCGCGCCC | 25831 |
rs189393756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134442 | GAACATTCCTAAGTA[G/T]TATGTGATTATATGG | 25831 |
rs189396218 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145407 | GTGGCTCATGCTTGT[A/T]ATCCTAGCACTTTGG | 25831 |
rs189409763 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176445 | ATACTTTAAATTTAT[C/T]AGTTTCAGTATCTAA | 25831 |
rs189427267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175656 | ATCACTTGAGGTCAG[A/G]AGTCCAAGACCAGCC | 25831 |
rs189452057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193641 | CAGAATAAAAACTTA[C/T]GGCTGGACGTGGTAG | 25831 |
rs189667026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130282 | TTATATTAAATAATT[A/C]AGTTCAATAAATTTG | 25831 |
rs189671553 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31119255 | AAGTTCCAGAGGTTA[A/G]AACCTGATTTTGGGG | 25831 |
rs189687849 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197399 | TCTTCTCTGTTACAA[C/T]GGCAGTACACAACTT | 25831 |
rs189706812 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192907 | ACTTGAACCCAGGAG[A/G]CGGAGGTTGCAGTGA | 25831 |
rs189716004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169869 | AGCCTGGTCTACAAG[A/G]GTGAAACTCCATCTC | 25831 |
rs189726544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167045 | AGGCAAGGCGGTATA[C/T]ATCTGTAGTCCTAGC | 25831 |
rs189748136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187912 | AAGCCACTGGGCCTG[A/G]CTAATTTTATTTTTG | 25831 |
rs189758700 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204146 | AATCCAGTCTATCAT[C/T]GATCGACATTTGGGT | 25831 |
rs189929809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148570 | GTAAATAAATATTTA[A/C]GAAAACACAGAAAAT | 25831 |
rs189937131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181086 | TTGATAGTCCAAGTA[C/T]CAAATGACAAGAATA | 25831 |
rs189951217 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115479 | AAACACTTTGCAGGC[C/T]AAGCACAGAGGCTCA | 25831 |
rs189953501 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149897 | GACAGAGTGAGACTC[C/T]GTCTCAAAAAAATAA | 25831 |
rs190110004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187192 | GTCTCTACTAAAAAA[C/T]ACAAAAAATCAAATT | 25831 |
rs190114199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137876 | AACAACTTCTAAATA[C/T]ACACAGTTTAAATAA | 25831 |
rs190118163 | snp | C/G/T | 0.000349949 | 0.0132232 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113070 | AAAGTCCAACAGTAA[C/G/T]AGAATGAAGAGTTCA | 25831 |
rs190124519 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178972 | CCTTATTCACTTAAA[A/G]TCCCAGAAGGCCAGG | 25831 |
rs190133002 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157447 | AAAAAATACAAAAAA[A/T]TGGGACTCAGCACTA | 25831 |
rs190133123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202420 | ACACCACCTGCCTTT[C/T]CTGACTAAACAGATG | 25831 |
rs190167611 | snp | A/C/T | 0.000322655 | 0.0126974 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127773 | ATACTTTCATTTTAA[A/C/T]TTACAACTTACCATA | 25831 |
rs190232237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141357 | ACTTTTAAAAAGAAC[A/C]ATTATTACTTAATAT | 25831 |
rs190238097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182186 | GATGTGAGCCACTGC[A/G]CCCAGCCTCTTTTTT | 25831 |
rs190344747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116861 | TGGTCTCAAACTCCT[A/G]ATCTCAAGTGATCTG | 25831 |
rs190360727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142343 | TAGATTACTAAGTGA[C/T]ATAATGTGATATATC | 25831 |
rs190377854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160157 | ACACAACAAAACCTA[C/T]GAGGTGGGTTTTATT | 25831 |
rs190385384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199248 | ATGCAGAAGCAGATA[C/T]GAGAATCCAGCTATC | 25831 |
rs190389951 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182638 | GGGCAGATCACTTGA[C/G]CTAAGGAGTTCGAGC | 25831 |
rs190455305 | snp | A/C/G | 0.000232537 | 0.0107804 | synonymous-codon, missense | HECTD1 | GRCh38.p7 | 14:31107011 | ACCTCGTGACTCATA[A/C/G]ATCAGTTTACTCATA | 25831 |
rs190483325 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121106 | ACAAATCTTAGATAC[C/T]ATATATTAACCATTT | 25831 |
rs190489372 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131208 | TAGCAAAAATAGGCC[G/T]TTCTTGAACGCTAAA | 25831 |
rs190496501 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164032 | TTATCAGACCTGTTC[A/C]AAATTCTATGTAGCT | 25831 |
rs190497138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159707 | GTGCGTGGCAGGATT[C/T]TGACTCACTGCAACC | 25831 |
rs190498519 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201334 | CTAGCACCTAAAAGC[A/G]TCTTCTGAGATGCTC | 25831 |
rs190638078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160476 | GTATTGAATGTGTAT[C/G]AGTACTGCATTCATA | 25831 |
rs190658512 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183083 | ACAAAAAAGGTAAAA[A/C]AAAATCCCAGATTCC | 25831 |
rs190670478 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200180 | TCATTCGACAAATCC[A/T]GACTATCTTGCCTTC | 25831 |
rs190728332 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145748 | TATATATGCAAAAGG[A/G]TAGCCACCTACTCAC | 25831 |
rs190731843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108027 | TTAAATCATTTGCTT[A/G]AAGAAATGATGGTGA | 25831 |
rs190740414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185681 | TGCAGTGAGCCATAA[C/T]TGTACATTGTACTCC | 25831 |
rs190760834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170570 | TTAAAAGTACTTGAA[A/G]GGGAAACTCTAAAAC | 25831 |
rs190764964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132053 | TCAAAGGGTTTATTT[A/G]AATAAATAAATGTCT | 25831 |
rs190767430 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152621 | GTAATCTCAGCACTT[G/T]GGAAGGCCAAGGCAG | 25831 |
rs190770295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156482 | TGCACTCCAGCCTGG[A/G]CAACAAGAGCGAAAC | 25831 |
rs190771149 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190230 | CCAGATATCGCAGAA[C/G]AGAGACAAGCCATCT | 25831 |
rs190776176 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112672 | TGGTGTGCAGTGGTA[C/T]GATCTCGGCTCACTG | 25831 |
rs190991736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137180 | CTGTTGCCCAGGCTA[A/G]AGTGCAGTGGAGTGA | 25831 |
rs190993073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101665 | GGCGTGGTGGCGCAC[A/G]CCTGTAATCCCAGCT | 25831 |
rs190997878 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124139 | GGAGCCACCTGCAAT[C/T]TAGGAACTGGTTGTG | 25831 |
rs191007836 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155985 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 25831 |
rs191022261 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176781 | TCTCTACTAAAAATA[C/T]AAAAAATTAGCCGCG | 25831 |
rs191027345 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137467 | GCACAGTGACTCAGA[C/T]CTGTAATCCTAGCAC | 25831 |
rs191027721 | snp | A/G | 0.000549647 | 0.0165687 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101314 | CCCTCACAAACCTCA[A/G]GAAACCAGGGCTAAA | 25831 |
rs191033377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177952 | CTCTAAGTGATGTTT[A/G]AATGAGCCAATACTC | 25831 |
rs191038577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146678 | GCCAACATGGTGAAA[C/T]CCCGTCTCTACTAAA | 25831 |
rs191257428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123179 | TTCTGCCACCACATA[C/T]AAGATGAGCACAGAC | 25831 |
rs191263804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102495 | AGTGCAATGGCATGA[C/T]CTTGGCTCACTGCAA | 25831 |
rs191277694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165748 | TCCTTGCCTTTGTAG[A/G]AATATAGCAGTACAT | 25831 |
rs191298026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124969 | TCCGCCACCACACCC[A/G]GTTAGTTTTTGTATT | 25831 |
rs191303648 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147748 | CATCAAGAGCGAAAC[C/T]GAGTCTCAAAAAAAA | 25831 |
rs191314144 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195024 | ATTTTAACTGAAAAA[C/T]CTGAACACATCTGGT | 25831 |
rs191333650 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133024 | ACTCAACTTACACTA[A/G]GCTTGATCACTTCCA | 25831 |
rs191340221 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171795 | GGAAATAAAAGGTTT[A/T]ATATCATTCTAATTT | 25831 |
rs191557578 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151080 | CCTGGGTAACAGATC[A/G]GGACTCTGTCTCTAT | 25831 |
rs191559716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117579 | ATGAATGTTTTCTTC[A/G]TTATCATGATCGTCT | 25831 |
rs191560915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108547 | GAATGTAAACAACTG[A/G]GCATGGTGGCTCAAG | 25831 |
rs191562838 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153164 | TTGGGAGGCCAAGGC[A/G]GGCGGATCACGAGGT | 25831 |
rs191590441 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189422 | AAAGATATATTTTTA[A/G]AACACAAATCTGTTA | 25831 |
rs191590949 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205157 | AGAGGGAAAAAAATG[C/G]CTGTAAGGTCTATCT | 25831 |
rs191592173 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191393 | AAGCCGGGTATGGTG[A/G]CACATGCCTGTAATC | 25831 |
rs191597908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158675 | TTGGCTGGGTGAGGT[A/G]GTTCACACCTGTAAT | 25831 |
rs191609130 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197412 | AACGGCAGTACACAA[C/T]TTCTTTCTGCCTAAA | 25831 |
rs191613775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181230 | AATACATTTCATGGG[C/G]GAATGTAGTATTTGC | 25831 |
rs191834645 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170133 | GACCAAAAAGTCAAC[C/G]AGGTGTGGTAGCTCA | 25831 |
rs191839422 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144666 | CCTCATAAAGCCATA[C/T]GAAAATGGGGAGCAG | 25831 |
rs191851675 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118962 | CATAGTTCTAGAGGT[A/C/T]GAATGCCTAAAATGG | 25831 |
rs191853002 | snp | A/C/T | 0.00518061 | 0.050666 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162476 | CCTATATATAACTGG[A/C/T]TCTATTGGGGGGACT | 25831 |
rs191864286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200711 | ACTTGAACCTGGGAG[A/G]TGGAGGTTGCAGTGA | 25831 |
rs191866988 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209916 | AACAAAAAACAAAAA[C/T]CCTTAACGTAGAAAG | 25831 |
rs191869484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184919 | AAAATACAGATAGTT[A/G]AGAGAATTGTATTAC | 25831 |
rs191884661 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142925 | ACACATGCACACACA[C/T]TAAAAAGAACTGAGT | 25831 |
rs192080774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165783 | CCAGCTCTCGTGGTG[C/T]TTACTTTAAAGAGAC | 25831 |
rs192090222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203409 | CTAACCCCTTCAACT[C/T]GAAATACTCTTGTAT | 25831 |
rs192129749 | snp | A/C | 0.000151397 | 0.00869916 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116210 | TAGGACATTATCTAC[A/C]AAAACATTAAGTTAA | 25831 |
rs192169226 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201248 | GGAAAGGGAAGACAA[C/T]GGACTTTTTACTGTA | 25831 |
rs192173793 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110158 | AGGTGTGTGCCACCA[C/G]GCCCAGCTAATTTTT | 25831 |
rs192176827 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134159 | TATTTTGTCTTTAAA[G/T]CATGAAAGGGGTGAA | 25831 |
rs192184374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173960 | CATATACTGCTAACT[C/G]TGTAATCCGAGGAAG | 25831 |
rs192190759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153526 | CCATTTCAACGTATT[C/T]TGAAGAGCGTAAGTG | 25831 |
rs192348794 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158171 | AACAAATTAGTATGC[C/T]TCCTTTCCCTTTTAT | 25831 |
rs192379795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196478 | GGCAGGTACAGGTCG[A/G]GCGCAGTGGCTCACA | 25831 |
rs192414872 | snp | C/T | 0.000367561 | 0.0135516 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112547 | TGCCAATGGTTCCTG[C/T]GAATTAACAAATAAT | 25831 |
rs192430281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147280 | GATCGCACCGCTGCA[C/T]TCCAGTCTGGGTGAC | 25831 |
rs192432619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134294 | ATAAATAAAATTTAG[C/T]AGAACTAATTTTTTA | 25831 |
rs192445653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154799 | TTCACCACCCTCGGG[A/G]TTCTACAATTATTAA | 25831 |
rs192456537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192282 | GGAGCTTGCAGTGAG[C/T]CAACATCCCTGTCAC | 25831 |
rs192461004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174795 | GAAAGAGGATGGAAT[C/T]ACCTCGATTTCATCA | 25831 |
rs192465170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187608 | ATACATACAGAAGAA[C/T]TGATCAAATAAATAT | 25831 |
rs192613779 | snp | C/T | 0.000581704 | 0.0170445 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103103 | AACACAAAAAACAAA[C/T]ATACAACTCAGTTTC | 25831 |
rs192618181 | snp | C/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147975 | AGGCAGGAGGATTAC[C/T]TGCACTCAGGTATTT | 25831 |
rs192631593 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188117 | TAGATAGATAGATAG[A/G]TAGATAGATAGATAG | 25831 |
rs192635890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128258 | AGCTAAGATCAATGT[A/G]GAGTCTAAACAAAAG | 25831 |
rs192641387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157797 | CAAAAACTAGCTAGA[C/T]GTGGTGGCAGGCACC | 25831 |
rs192664500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104330 | AAAATACCCATTACC[A/G]ATGAAATGGACAGAA | 25831 |
rs192664737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195276 | TGCAATTCATTCAAC[A/G]CATCTATTGAATGCC | 25831 |
rs192674169 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179755 | TTCTAGTTTCTCTAG[A/G]CAGACTAAACTACAG | 25831 |
rs192725660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138805 | ATCACTCATTAAAGG[C/T]TATTATTCAAAAGAA | 25831 |
rs192734847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180937 | CTACATATGCTCTAT[A/G]TATGCATATGTAGTA | 25831 |
rs192861905 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126927 | CCTCCCACCTTGGCG[C/T]CCCAAAGTGCTGGGA | 25831 |
rs192869156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167317 | AAAAGTACAATCTGG[A/T]CATGGTGGCATACTT | 25831 |
rs192922622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163192 | CTTTGGGAGGCTGAC[A/G]TCGGAAGATCGCTTG | 25831 |
rs192924802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120022 | TACATACATTTCTTC[A/T]TCATTTCAGTTTACC | 25831 |
rs192926618 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191958 | AGGTTGCAGTGAGCC[A/G]AGATCACACCATTGC | 25831 |
rs193040470 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111054 | CCATTTTCTAACCAA[C/T]TGAGTAATTTGTTGC | 25831 |
rs193042852 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143371 | GTGAGTCAGGACTGC[A/G]CCACTGCACTCAAGC | 25831 |
rs193047884 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183861 | CACAGGCATGCACCA[A/C]CATACCCAGTTAATT | 25831 |
rs193135535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138189 | ATATTATAAAATCCA[A/G]AACACTTCTGGTTCC | 25831 |
rs193146878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167945 | CAAGGGGAAGAGTAA[A/G]CAAGAGCCAAATCTC | 25831 |
rs193151029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206691 | AGGTTACGGATCCGA[A/G]CGAATGTAGGCCAAC | 25831 |
rs193166235 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145453 | AGATCACTTGAGGTC[A/C]GTCAGGAGTTCAAGA | 25831 |
rs193167437 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185247 | CTTGGGAGGCTGAGG[C/G]AGAATGGTGTGAACC | 25831 |
rs193218944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118192 | TGTATTTTTAAGTAG[A/G]GACGGGATTTCACCA | 25831 |
rs193228777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160882 | CACTAGTTGCCCAGG[A/C]TGGTCTCAAACTCCT | 25831 |
rs193228960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200431 | CGGGAGGATCACTTA[A/G]GCTCAGGAGTTCTAG | 25831 |
rs193284841 | snp | A/G/T | 8.29153e-05 | 0.00643823 | synonymous-codon, intron-variant | HECTD1 | GRCh38.p7 | 14:31113934 | AATACTTTTATTAGT[A/G/T]CCAGTTAATTTCCAG | 25831 |
rs193301542 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188130 | AGATAGATAGATAGA[C/T]AGATAGATAGATAGA | 25831 |
rs199501211 | snp | C/T | 0.000149235 | 0.00863686 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31113966 | GGCGCAGGAAAGCAG[C/T]GTCTGCATTCTTCTG | 25831 |
rs199517581 | snp | A/C | 1.65685e-05 | 0.00287819 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136532 | TGCCAGAAACTCACC[A/C]TTTTCAAAAGGTACT | 25831 |
rs199518256 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194823 | ATTTCCCTGGGAACT[C/G]TAATATTTTCTGTAT | 25831 |
rs199529960 | snp | A/C | 0.00199795 | 0.0315433 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135491 | TTTGCATTTGTTCCA[A/C]TCCAGTAAATGATTC | 25831 |
rs199542298 | in-del | -/A/AA/AG | 0.0292022 | 0.117795 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147755 | GCGAAACCGAGTCTC[-/A/AA/AG]AAAAAAAACATTACA | 25831 |
rs199554447 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198206 | CTACTTAAAGGAAAT[C/T]GGAATTAATTATAAA | 25831 |
rs199574833 | in-del | -/TAATCC | 0.0185938 | 0.0946107 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103286 | GGTGGCTCACGCCTG[-/TAATCC]CAGCACTTTGGGAGG | 25831 |
rs199605034 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164560 | TTATTCTCACTCCTA[A/G]AGAGGATTAAGTATA | 25831 |
rs199605586 | snp | C/G | 1.65699e-05 | 0.00287831 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128844 | GTTACTTGCTGAAGA[C/G]CTAAGAGGTCGTTGT | 25831 |
rs199633695 | snp | C/T | 1.66818e-05 | 0.00288802 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171929 | TTTGACCTCTATTAA[C/T]ATCTGCACCTCTCTC | 25831 |
rs199747097 | snp | A/C | 0.00199792 | 0.0315431 | missense | HECTD1 | GRCh38.p7 | 14:31109533 | GGGTCATCTCGCCTA[A/C]CACTGCTTGTGGTTC | 25831 |
rs199760699 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131044 | AAAAAAAAAAAAAAA[A/T]AGAGTCAGTAATGAC | 25831 |
rs199790764 | snp | C/T | 3.33611e-05 | 0.00408405 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173168 | GACCTCCTGTGTCAA[C/T]TGCATCTATAAGTGC | 25831 |
rs199851138 | in-del | -/A | 0.0193772 | 0.0965046 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184282 | GGGAGACCCGTCTCT[-/A]AAAAAAAAGATTAAA | 25831 |
rs199851699 | snp | C/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175059 | AGATGTCCACTGTCA[C/T]GAATGAAGGTAAGCA | 25831 |
rs199853360 | snp | A/G | 0.001998 | 0.0315438 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31113431 | ATCACTACTTTGAAG[A/G]GTAGAAATGGCCCCC | 25831 |
rs199870893 | snp | A/G | 0.000116199 | 0.00762142 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168468 | AACTGGACACATCCA[A/G]TCACCTACAGACAAA | 25831 |
rs199911191 | in-del | -/A | 0.0205511 | 0.0992634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126681 | AGATAATTGCAATTT[-/A]AAAAAAAAATATTTT | 25831 |
rs199922241 | snp | C/T | 0.00199808 | 0.0315444 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171957 | CTCACAAAGAAATTC[C/T]ACCTGTAAAATGATA | 25831 |
rs199992307 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141323 | AAAGAATTATTTTTT[-/A]AAAAAAAAACAGTAT | 25831 |
rs200021018 | in-del | -/A | 0.00949659 | 0.0682503 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141979 | AAAAGTATAAAGTCC[-/A]AAAAAAAAATAATTT | 25831 |
rs200055858 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136038 | AAACAACAACAACAA[-/C]AAAAACAAAAAACAA | 25831 |
rs200056052 | snp | A/G | 0.00432728 | 0.0463132 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114269 | CAAGAGTAAACCAAT[A/G]TTCTAAAATAACTTA | 25831 |
rs200060759 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198879 | TAAAATACTAAAAAT[-/A]AAAAAAATTATTCCA | 25831 |
rs200069531 | snp | C/T | 0.000248449 | 0.0111428 | missense | HECTD1 | GRCh38.p7 | 14:31116327 | GTACATAGTAAAAGA[C/T]GGTTGATCTGAAATT | 25831 |
rs200107470 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201526 | TTTTTTTTTTTTTTT[-/T]GGAGGCACGGTCTCA | 25831 |
rs200112692 | snp | A/G | 6.63614e-05 | 0.00575989 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156899 | GACCTGCCAACGTTG[A/G]CACTTTGCTAATTAC | 25831 |
rs200113105 | snp | C/G | 1.65641e-05 | 0.00287781 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31174995 | CTCCATTTTGCCACA[C/G]AGTCTTGATACCACA | 25831 |
rs200113675 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108113 | ATTTTTATTTTTTGA[C/G]ACAGTTTCACTCTTG | 25831 |
rs200145217 | snp | G/T | 2.13117e-05 | 0.00326426 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135232 | TTAGCAAATAACAAC[G/T]TTAAGATAATTGCAT | 25831 |
rs200153888 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161763 | TTTTACTAAAAACAC[-/A]AAAAAAATTAGCCGG | 25831 |
rs200195698 | snp | C/T | 0.00199806 | 0.0315443 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100903 | GTATTTTTAAAGTCT[C/T]TGATGTCTCCCATTG | 25831 |
rs200217364 | in-del | -/T | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099859 | GTTGTGGATCTGGTG[-/T]TTTTTTAAAAAAATA | 25831 |
rs200218114 | snp | C/T | 1.65723e-05 | 0.00287852 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135660 | ACCTTAATAATGCTG[C/T]TTTCAAGCACGTTAC | 25831 |
rs200221120 | snp | C/G/T | 0.000416958 | 0.014433 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107203 | TGTGAACAGTCCACA[C/G/T]GACCTCTGCACATAA | 25831 |
rs200234047 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171825 | TTTAAACCATGTAAA[C/T]GTTAAAAATTAGTAA | 25831 |
rs200236317 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162864 | CTAGAGCTTAAGAGT[C/T]CAAGACCAGTCTGGG | 25831 |
rs200294919 | snp | A/T | 2.3751e-05 | 0.003446 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114274 | GTAAACCAATGTTCT[A/T]AAATAACTTACCATT | 25831 |
rs200314145 | in-del | -/ATACT | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114913 | ATATCACTGTACTGA[-/ATACT]ATAGGCAACTGTAAC | 25831 |
rs200340911 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203677 | AGCTGTTATGTTAGG[-/A]ATGGAAGGATTTTAC | 25831 |
rs200350849 | snp | C/T | 0.000287549 | 0.0119872 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141949 | TCATATCCAAATCCA[C/T]GCTCTAAAGAAAACA | 25831 |
rs200369416 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146497 | GACGTACCTTGCAAG[-/A]AAAAAAAAAAAAAAG | 25831 |
rs200388092 | snp | A/G | 7.70228e-05 | 0.00620528 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141881 | ATCTTCATTTTCACT[A/G]AAGGCAGTTTTAAAA | 25831 |
rs200392734 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163095 | CACACACACACACAC[A/G]CACACATGCGCACAC | 25831 |
rs200396981 | snp | A/G | 3.4002e-05 | 0.00412309 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175141 | TCAGTTCTAATACCT[A/G]TAATAGTAAAACAAA | 25831 |
rs200406043 | in-del | -/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31210018 | TTACCAAGTTTTTTG[-/T]TTGTTTTTTTTTTTT | 25831 |
rs200409299 | snp | G/T | 0.000778797 | 0.0197178 | missense | HECTD1 | GRCh38.p7 | 14:31106685 | GGCCCAGAACCTGAT[G/T]GATTCTTCAGCACTA | 25831 |
rs200417980 | snp | A/C | 9.9369e-05 | 0.00704802 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168393 | CGGATCTCCTTTGGG[A/C]TCATTACATTCTTCT | 25831 |
rs200437817 | in-del | -/AT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139059 | TATATATATATATAT[-/AT]CTGTATGGGGAGGAG | 25831 |
rs200455930 | snp | A/C | 0.00013849 | 0.0083202 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129441 | ATCCCAGGTGACATC[A/C]ATCCAGCCTGGAAAG | 25831 |
rs200510869 | snp | G/T | 6.62932e-05 | 0.00575693 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128651 | CCAAAGTATTAGTGT[G/T]GTTATCACTGCTGCT | 25831 |
rs200525146 | snp | A/T | 0.000183479 | 0.00957631 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205757 | GAAAACAGATGTCAC[A/T]ACAGTAACCCAAAGG | 25831 |
rs200557185 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205185 | TCTAGTAAGAATTCT[C/T]TTTTATATTTTTGCA | 25831 |
rs200562961 | snp | C/T | 8.70163e-05 | 0.0065955 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157327 | GTAAAAATAGAATTA[C/T]ATGAAGCCAAATGAA | 25831 |
rs200581021 | snp | C/T | 8.28041e-05 | 0.00643391 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134997 | ACGAGCATGACGAAG[C/T]GTATATGCTGATGGT | 25831 |
rs200606968 | in-del | -/A | 0.424503 | 0.179021 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178808 | AACTCTGTTTCAAAG[-/A]AAAAAAAAAAAAAAA | 25831 |
rs200609915 | snp | C/T | 0.00013249 | 0.00813802 | missense | HECTD1 | GRCh38.p7 | 14:31113366 | ACTCCACAAGAGTTC[C/T]GTCCATTGCCTGCTT | 25831 |
rs200613295 | in-del | -/AT | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103658 | CACATGTTCCCACTC[-/AT]ATGTGGGAACTTAAA | 25831 |
rs200618942 | in-del | -/GAGAT | 0.0111196 | 0.0737302 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194953 | GCATTATCTGTAGTA[-/GAGAT]ATTTTATAAAATAGT | 25831 |
rs200629266 | snp | A/C | 2.51531e-05 | 0.00354626 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171839 | ATGTTAAAAATTAGT[A/C]ATTTTAAAACCTAGA | 25831 |
rs200644301 | in-del | -/AG | 0.0611083 | 0.163768 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141110 | TTTTGTATTTTTAGT[-/AG]AGAGATGGGTTTTTG | 25831 |
rs200674201 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110966 | TGCTTTTTTTTTTTT[-/T]GGTAAATTACTTCTT | 25831 |
rs200688605 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31140932 | CATCCAGGTTTTTTT[C/T]TTTTTTTTTTTTTGT | 25831 |
rs200703652 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165016 | AAAAAAAAAAAAAAA[C/T]TGACCCCACTAACAC | 25831 |
rs200710585 | snp | A/C | 0.00199793 | 0.0315432 | missense | HECTD1 | GRCh38.p7 | 14:31113442 | GAAGAGTAGAAATGG[A/C]CCCCTGGTTTAACCC | 25831 |
rs200720993 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122639 | TATAGGGCTCATGCC[C/T]TGTAGTCCCACACTT | 25831 |
rs200735609 | snp | A/G | 0.000265015 | 0.0115081 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128676 | GCTGCTTCGGCTTAG[A/G]TTCATGTTGTTCGTG | 25831 |
rs200750894 | snp | A/G | 1.99043e-05 | 0.00315464 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107272 | ATTTTTTAGAGGGTG[A/G]AATGCAAATAAAATT | 25831 |
rs200752669 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147756 | CGAAACCGAGTCTCA[-/G]AAAAAAACATTACAA | 25831 |
rs200786425 | snp | C/T | 5.07765e-05 | 0.00503842 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103084 | ACATCGTACATGTAA[C/T]GGAAACACAAAAAAC | 25831 |
rs200789351 | in-del | -/TGA | 0.0322114 | 0.122752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159075 | TCATTACCCTTGAGG[-/TGA]TGAATGATAGAAGGA | 25831 |
rs200837832 | snp | A/C/G | 5.37142e-05 | 0.00518215 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144957 | CTACCAAAATAAACA[A/C/G]AACAAATGTGAATTT | 25831 |
rs200859914 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122638 | AAAGTGTGGGACTAC[-/A]GGGCATGAGCCCTAT | 25831 |
rs200966445 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161386 | AGTTCAAGACCAGCC[-/T]TGGGCAGCAAAGCAA | 25831 |
rs200979112 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127155 | TTTTTTTATATTTTT[-/A]GTAGGGACAGGGTTT | 25831 |
rs200985475 | snp | C/T | 0.000298048 | 0.0122039 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129200 | CGCTGCTACTGGCCA[C/T]GCTACACACAGAACT | 25831 |
rs200999293 | in-del | -/TAGA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188145 | AGATAGATAGATAGA[-/TAGA]CAGACAGATAAAAGC | 25831 |
rs201032124 | snp | C/T | 0.00299988 | 0.0386127 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141828 | TGTGAACATTACAAA[C/T]ATCAAATTCAAAGAA | 25831 |
rs201039125 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177989 | GAGAGGTCTGAGAAA[A/G]ATAAGTAATGAGCCA | 25831 |
rs201053234 | in-del | -/TC | 0.0158469 | 0.0875917 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205182 | CTATCTAGTAAGAAT[-/TC]TCTTTTATATTTTTG | 25831 |
rs201057899 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175732 | AGCCGGGCATGGTGG[C/T]GCATGCCTCTAATCC | 25831 |
rs201059078 | in-del | -/A | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099865 | ATCTGGTGTTTTTTT[-/A]AAAAAAATAACACAA | 25831 |
rs201071378 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173254 | GAACTATCTAATCTC[C/T]GGAGTCCTGGGATTC | 25831 |
rs201085212 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180124 | GGAGGTTGCAGTGAG[-/C]CTGAGATCATGCCAC | 25831 |
rs201100670 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206621 | CTATTCTTAAAAGTT[-/A]AAAAAATAAAAAAAT | 25831 |
rs201122171 | snp | A/C/T | 1.74251e-05 | 0.00295165 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128579 | CCTCCAAGTGGAAAA[A/C/T]GCATCGGATTCCAGA | 25831 |
rs201127730 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141658 | TTCATACCAGACATG[C/T]AATTTCAATGTTTCT | 25831 |
rs201165704 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161647 | GCCAGGCTGGGTGTG[A/G]TGGATCACGCCTGTA | 25831 |
rs201170424 | snp | G/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208416 | CGTTTCTTGTGGCTT[G/T]TGGTCACAAGTATGT | 25831 |
rs201177803 | snp | A/G | 0.000447461 | 0.0149509 | missense | HECTD1 | GRCh38.p7 | 14:31116401 | ACTTTCAAAGTGAGA[A/G]CTAATCGAGGTGACG | 25831 |
rs201189823 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136834 | TTTTTTTTTTCTTTT[-/G]TTTCTGAGACGGAGT | 25831 |
rs201189912 | snp | C/T | 4.99397e-05 | 0.00499673 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31106927 | TTCAAAGCTTCCTAC[C/T]GAGAGTGAATCATGA | 25831 |
rs201192053 | snp | G/T | 0.000780361 | 0.0197376 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175008 | CAGAGTCTTGATACC[G/T]CAGCCATAGCAGAGT | 25831 |
rs201192424 | snp | A/G | 1.66568e-05 | 0.00288585 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31172104 | TGACCTACATCATCC[A/G]TAAAATTTACTTCAA | 25831 |
rs201210477 | snp | A/G | 0.000182172 | 0.00954216 | missense | HECTD1 | GRCh38.p7 | 14:31113328 | CTATATATAGAATAC[A/G]CAGAAGCTGAAGGAC | 25831 |
rs201227255 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131656 | TGGGAAAAAAAAAAA[-/A]GATTCTAATTTCCCT | 25831 |
rs201289790 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108115 | TTTTATTTTTTGAGA[C/G]AGTTTCACTCTTGTC | 25831 |
rs201294046 | snp | C/G/T | 0.00124424 | 0.0249146 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144925 | TCATCGTATAAATCT[C/G/T]GAGCCATAGTTCGTA | 25831 |
rs201296724 | snp | C/G | 5.21889e-05 | 0.00510801 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128584 | AAGTGGAAAAAGCAT[C/G]GGATTCCAGAAGGAA | 25831 |
rs201335906 | snp | C/T | 0.000224616 | 0.0105952 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171871 | TTTACCTTTGCTACT[C/T]GAGGTCTTCCAAAAC | 25831 |
rs201349754 | in-del | -/A | 0.288906 | 0.246954 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176613 | GAAGCAGAAATCATT[-/A]AAAAAAAAAAAAAAC | 25831 |
rs201363692 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155361 | AAAAAAAAAAAAAAG[C/T]AAAAGAGCAACTTTA | 25831 |
rs201419755 | snp | G/T | 0.0019855 | 0.0314453 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107208 | ACAGTCCACATGACC[G/T]CTGCACATAATATCC | 25831 |
rs201422760 | snp | C/T | 0.000414425 | 0.0143889 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31113950 | CCAGTTAATTTCCAG[C/T]GGCGCAGGAAAGCAG | 25831 |
rs201423459 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190170 | GTGATTCTAGTGCCT[A/C]AGTGTCAAGTCACTT | 25831 |
rs201433907 | in-del | -/AAC | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204462 | TTTTTTAAATGTCAT[-/AAC]AAATACTTCTACTAC | 25831 |
rs201452780 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141318 | CTAACAAAAGAATTA[-/T]TTTTTAAAAAAAAAC | 25831 |
rs201470236 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198205 | TCTACTTAAAGGAAA[G/T]GGGAATTAATTATAA | 25831 |
rs201479254 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100913 | AGTCTCTGATGTCTC[C/T]CATTGCACTTCAAAG | 25831 |
rs201513517 | snp | C/T | 8.29098e-05 | 0.00643801 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133324 | AGGCCTCTGATAACA[C/T]GAGCTCCTGGAACCA | 25831 |
rs201518177 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161882 | TCTCAAAAAAAAAAA[-/G]AAAAAGAAAAAGCCA | 25831 |
rs201555948 | snp | C/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149139 | GCTCTTTGTAACTTC[C/T]CTAAGAATTCACTTC | 25831 |
rs201565147 | snp | A/G | 0.000265221 | 0.0115126 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133552 | AGTGCCATAAAGTTC[A/G]AATCCAGATAATGAG | 25831 |
rs201606450 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114420 | TCTTTAAAAAAAAAA[-/A]GTGAATGTCATTCAC | 25831 |
rs201612618 | snp | A/G | 0.00303203 | 0.0388178 | missense, nc-transcript-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121393 | ATTACCTGCTCCCCA[A/G]TAGGTCGGCTCCCTG | 25831 |
rs201618596 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205188 | AGTAAGAATTCTCTT[A/T]TATATTTTTGCATAT | 25831 |
rs201644031 | snp | A/G | 4.98683e-05 | 0.00499316 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100928 | CCATTGCACTTCAAA[A/G]CTCAATTGAGATGAA | 25831 |
rs201665264 | in-del | -/AAT | 0.0952156 | 0.196321 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179468 | AAACAAAATAAAATA[-/AAT]AATAATACTTTATAT | 25831 |
rs201677714 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103554 | TCTCAAAAAAAAAAA[-/A]GAATGAAATCTTTTC | 25831 |
rs201715747 | in-del | -/C | 0.0184945 | 0.0943675 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148867 | ATTCATTTATTTGTA[-/C]CCAATAAACTTACAT | 25831 |
rs201746712 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185369 | CAGAAAAAAAAAAAA[-/C]CTGATGCTTCCACTG | 25831 |
rs201749539 | in-del | -/A | 0.00835141 | 0.0640778 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209921 | AAAACAAAAACCCTT[-/A]ACGTAGAAAGAGGAC | 25831 |
rs201768472 | in-del | -/AC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122254 | ACTGGCTAAGTTCAT[-/AC]ACACACACGTGTGTG | 25831 |
rs201775705 | in-del | -/G | 0.272241 | 0.249009 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118895 | AAGACTCCATCTCAA[-/G]GGGAAAAAAAAAAAA | 25831 |
rs201824279 | snp | C/T | 0.00199798 | 0.0315436 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173288 | CTGTAGATCCAGCAC[C/T]AGACTTTGGCAAAGC | 25831 |
rs201841312 | snp | C/T | 6.69053e-05 | 0.00578344 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171974 | CCTGTAAAATGATAA[C/T]GAATCATAAAGCTGC | 25831 |
rs201841460 | snp | A/G | 9.93937e-05 | 0.0070489 | missense | HECTD1 | GRCh38.p7 | 14:31116371 | TCAACTTCACGAGTC[A/G]TTCCAAGACCTGTTA | 25831 |
rs201913051 | in-del | -/TC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188241 | GTTATTCTTCCTTTT[-/TC]TTTTTTTTTTTTGAG | 25831 |
rs201960889 | in-del | -/CTAA | 0.0126979 | 0.078662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169081 | GGTCAAACTACCTAT[-/CTAA]CTAAACAATACCAAA | 25831 |
rs201965003 | snp | A/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163922 | TGTCTCAAAAAAAAA[A/T]TTTTTTTTTCAAAAG | 25831 |
rs201977346 | snp | C/T | 1.68641e-05 | 0.00290375 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148712 | ATAAAGCACATCCAA[C/T]AGATATACCTTTTGC | 25831 |
rs201987452 | in-del | -/CTTT | 0.0123036 | 0.0774623 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197956 | TCTCTTCTTGAATCA[-/CTTT]CTTTCCTGTGTTGAC | 25831 |
rs201992770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140010 | CGACTGCGAAGAAAT[A/T]ATTATTATTAAGAGG | 25831 |
rs202002953 | snp | A/G | 0.000132523 | 0.00813903 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31102945 | ACCCAGCTTAGGTTC[A/G]GTGTAATTGATAATA | 25831 |
rs202003109 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192975 | GCGAGACTCCACCTC[-/A]AAAAAAAAATAAAGT | 25831 |
rs202003389 | snp | C/T | 3.32198e-05 | 0.00407539 | missense | HECTD1 | GRCh38.p7 | 14:31106982 | TGACTTTCAGTACAG[C/T]GTAAGTCTCTATCAC | 25831 |
rs202019278 | in-del | -/ATA | 0.0410537 | 0.137264 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128194 | TTATAGCACTATTAT[-/ATA]ATTACTTTGACCTGT | 25831 |
rs202075322 | snp | A/G | 0.000232011 | 0.0107681 | missense | HECTD1 | GRCh38.p7 | 14:31116258 | TGGGCTCCCAAATAC[A/G]CCTAAGTTTATCTGA | 25831 |
rs202081153 | in-del | -/CAGA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188153 | AGATAGACAGACAGA[-/CAGA]TAAAAGCTAATGTGT | 25831 |
rs202081429 | in-del | -/G | 0.0217236 | 0.101931 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182743 | TAGTCCCAGCTACTT[-/G]GAGAGGCTGAGGCAG | 25831 |
rs202093712 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127870 | AGTGTTACTTAAAGA[C/T]TGACCAACTGATAAA | 25831 |
rs202106329 | snp | C/G/T | 1.70717e-05 | 0.00292157 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175145 | TTCTAATACCTATAA[C/G/T]AGTAAAACAAATGTA | 25831 |
rs202123698 | snp | C/T | 0.000165948 | 0.00910748 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119904 | ACAAACATAATAAGA[C/T]GCAAAATTTCATTGT | 25831 |
rs202133227 | snp | C/T | 0.000115924 | 0.00761239 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129154 | ACAATTTCTGATCTC[C/T]GTTCCGTTTTGGTCG | 25831 |
rs202139994 | snp | C/T | 0.00295525 | 0.0383261 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168499 | TATTTTTTAAAGAAA[C/T]ACTTTTTTGGAAACT | 25831 |
rs202153741 | in-del | -/AAAG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161598 | AAAAAAAAAGAAAAA[-/AAAG]AAAGAAAGAAAGGAA | 25831 |
rs202189034 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171326 | CTGAGGCACGAGATC[A/G]TTTGAACACAGGAAT | 25831 |
rs202192238 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134567 | GTGTGTGTGTGTGTG[C/T]GCGCGCGTATGTATA | 25831 |
rs202206159 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125972 | TATTACTTTAAGCAT[C/T]TATCCTAAGGAAGTA | 25831 |
rs202221885 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102426 | CATGATGTCAGTTGT[C/T]TTTTTTTTTTTTTTT | 25831 |
rs202224179 | in-del | -/AT/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206627 | TAAAAGTTAAAAAAA[-/AT/T]TAAAAAAATTAAAAA | 25831 |
rs207474615 | snp | A/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208753 | TGCAAAAAAATTAAA[A/G]TTTAAAAAATAATTA | 25831 |
rs267603978 | snp | A/G | | | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178236 | GCAAAGGGCTGGTAA[A/G]AAAGTGCGAGGAGGA | 25831 |
rs367624270 | snp | A/G | 6.63262e-05 | 0.00575836 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136510 | AATGCTTATTTCACC[A/G]TGCCCTTGCCAGAAA | 25831 |
rs367624417 | snp | A/G | 1.65957e-05 | 0.00288055 | missense | HECTD1 | GRCh38.p7 | 14:31112438 | CGCCAAATGCTGTAC[A/G]TGTGAAATAAAGCTG | 25831 |
rs367628894 | snp | C/T | 1.65619e-05 | 0.00287762 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173287 | CCTGTAGATCCAGCA[C/T]TAGACTTTGGCAAAG | 25831 |
rs367632349 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199306 | TTGCAAAAATGTAAA[C/T]TAATGCCTCTATTCT | 25831 |
rs367637104 | snp | A/C | 8.28109e-05 | 0.00643418 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128963 | CCCCAGGAGTACGAA[A/C]AGAACTATCAGGGCC | 25831 |
rs367653309 | snp | A/G | 3.31334e-05 | 0.00407009 | missense | HECTD1 | GRCh38.p7 | 14:31116366 | GTAATTCAACTTCAC[A/G]AGTCGTTCCAAGACC | 25831 |
rs367654084 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175162 | GTAAAACAAATGTAA[C/T]GAAAGAATGCAAGCC | 25831 |
rs367679690 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31119896 | TTTCACACACAAACA[A/T]AATAAGATGCAAAAT | 25831 |
rs367691618 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163071 | TCCTGACACACACAC[A/G]CACACACGCACACAC | 25831 |
rs367708914 | snp | A/G | 1.66902e-05 | 0.00288874 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205752 | TGGTTGAAAACAGAT[A/G]TCACTACAGTAACCC | 25831 |
rs367724968 | snp | A/C | 0.000167986 | 0.00916322 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169398 | CTATGGCCCCTTTCT[A/C]GAGCTTTATCTAATG | 25831 |
rs367727244 | snp | A/G | 0.000115978 | 0.00761415 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31123004 | GTCCTCATCATCATC[A/G]AGCTCAGCCAATAGA | 25831 |
rs367742562 | snp | A/G | 1.65633e-05 | 0.00287774 | missense | HECTD1 | GRCh38.p7 | 14:31113402 | TGAGGTTGTTCTTTT[A/G]TTAAATTAAGAATAT | 25831 |
rs367754588 | snp | A/G | 5.46861e-05 | 0.00522877 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144121 | CTTACATTGTTTAAC[A/G]CAGTAAGAAGTGCTT | 25831 |
rs367786150 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129900 | CTCCTGGGCTTAAAC[A/G]ATCCTCCCACCTCAG | 25831 |
rs367792663 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126385 | TGAATCAAATACATC[C/G]CTTTGATTATAGCAT | 25831 |
rs367800413 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184130 | AAAACACTATTAGAA[A/G]ATTCCTAACAAAAGT | 25831 |
rs367809931 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165971 | CTGACTCACCCTCCC[A/G]AGTAGCTGGGACTAC | 25831 |
rs367830418 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181964 | AGTGACACCATTTCG[A/G]CTCACTGCAACCTCC | 25831 |
rs367837946 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147078 | CTACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 25831 |
rs367850312 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141698 | ATTAGATTAAAAAAA[A/G]CTTCAAAAATTTTCC | 25831 |
rs367872910 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152346 | AGCTATTCTGCCACC[A/C]TGCAATGACAATTTT | 25831 |
rs367873269 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198736 | TAAGTTCACTGATAT[A/G]ATATCAGAATCCACA | 25831 |
rs367891342 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115588 | ACATGGTAAAAACCC[C/T]ATCCCTACAAAAAAT | 25831 |
rs367948054 | in-del | -/A | 0.0275645 | 0.114116 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124050 | TAACCTTAGTAACAG[-/A]AAAAAAATGGTGTGT | 25831 |
rs368120201 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132326 | CCTATAATCCTAGCT[A/C]GTCAGGAGGCTGAGA | 25831 |
rs368158052 | snp | C/T | 5.01023e-05 | 0.00500486 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112408 | AACATAAAAAAAAGG[C/T]TTCTTACCTTGAGGC | 25831 |
rs368161791 | snp | A/C/G | 6.63607e-05 | 0.00575991 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136704 | TCTGGAAAACGTCTT[A/C/G]GTTTCTGTCTCAGAA | 25831 |
rs368167266 | snp | C/G | 1.70217e-05 | 0.00291729 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173707 | TTCGAGATAACAGCT[C/G]CTCAGTTAATCCATG | 25831 |
rs368175327 | snp | C/T | 1.65611e-05 | 0.00287755 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150174 | GTCTCTCCAATGATA[C/T]GGTTTACCTTGTTGC | 25831 |
rs368259496 | snp | A/C | 1.7461e-05 | 0.00295469 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178272 | GTAGTGAAAGAAATC[A/C]TATTACATCTAGGGT | 25831 |
rs368272204 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166818 | ATTGTGCCACTGCAC[C/T]CCAGCCTGGACAAGA | 25831 |
rs368282298 | snp | A/G | 0.000596017 | 0.0172526 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122926 | TACCATAACCTCCTC[A/G]TATTCTTGGTCCTCC | 25831 |
rs368286199 | snp | A/G | 0.000144648 | 0.00850312 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141950 | CATATCCAAATCCAT[A/G]CTCTAAAGAAAACAA | 25831 |
rs368302820 | snp | A/T | 4.98509e-05 | 0.00499229 | missense | HECTD1 | GRCh38.p7 | 14:31107118 | GAATGCATTTGGCCA[A/T]GAAAATTCCAAGGAA | 25831 |
rs368339043 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134834 | ATAAACAAAGCTCTT[C/T]AGTGAGTTTTCCAAT | 25831 |
rs368372102 | snp | A/G | 1.75452e-05 | 0.00296181 | missense | HECTD1 | GRCh38.p7 | 14:31109573 | CCACAGTGGCTTCAC[A/G]TCGGTTCTGTAACCA | 25831 |
rs368383250 | snp | A/G | 1.6569e-05 | 0.00287824 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136668 | TCCTTGTAAGTATCT[A/G]CACAAAAACGATCAA | 25831 |
rs368384046 | snp | G/T | 0.000118818 | 0.00770682 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149978 | AACTAGGAAAATATT[G/T]TAATTGAAACAAAAT | 25831 |
rs368406709 | snp | A/T | 1.65677e-05 | 0.00287812 | missense | HECTD1 | GRCh38.p7 | 14:31102942 | ATAACCCAGCTTAGG[A/T]TCAGTGTAATTGATA | 25831 |
rs368423225 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134055 | TTAAAAAAAAAAAAA[-/AAAAAAAAAAAAAA]GGATGGTTTACAAAG | 25831 |
rs368427918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137200 | CAGTGGAGTGATCTC[C/G]GTTTACTGCAACCTC | 25831 |
rs368434449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134087 | GTAGGAGAAATTCTC[C/T]TATGATGGAAAAACG | 25831 |
rs368443455 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176749 | GAGACCAGCCTGGCC[A/G]ACATGGTGAAACCCC | 25831 |
rs368454649 | in-del | -/GGCT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111548 | TGAGCCACCGCGCCT[-/GGCT]ATTTTTTTTAAACAC | 25831 |
rs368475593 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158552 | GGCGTGAGCCACCAC[A/G]CCCGGCCAAATTAAC | 25831 |
rs368495828 | snp | C/T | 5.00204e-05 | 0.00500077 | utr-variant-5-prime, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205954 | TTTTTTAAAAGTCTC[C/T]TTGCTTAAATTTGAA | 25831 |
rs368503213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163511 | GGGAGGCTGAGTTGG[A/G]AAAATCCCTTGAGCC | 25831 |
rs368510665 | snp | A/G | 1.66846e-05 | 0.00288826 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173452 | AATGGGAAGAAAGAT[A/G]TTTAATATATTAGCA | 25831 |
rs368513885 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130816 | CATAAGTAGCTTAGA[C/T]GAGATTTTTCAATTG | 25831 |
rs368546653 | in-del | -/AG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108116 | TTATTTTTTGAGACA[-/AG]GTTTCACTCTTGTCG | 25831 |
rs368558082 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195790 | GCCTCCCATAGTGCT[C/G]GGATTACAGGCATGA | 25831 |
rs368615406 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146473 | TGTTTCTAAGCACAA[A/G]GAGACTGTGACGTAC | 25831 |
rs368618062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141022 | AACTTCTGCCTCCAG[A/G]GTTCAAGGGATTCTC | 25831 |
rs368630382 | snp | C/T | 8.29621e-05 | 0.00644004 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133294 | CTGCCATCCTGATCT[C/T]GCCATTTCCAATCCA | 25831 |
rs368655114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188658 | TTCTTCTTATCCATT[A/G]TAACTCTCTCCTAAA | 25831 |
rs368657367 | snp | C/G | 1.68255e-05 | 0.00290043 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113520 | ACTGGCCATTAATCA[C/G]ATTTTCAAGAAAAAC | 25831 |
rs368701440 | snp | C/G | 1.66538e-05 | 0.00288559 | missense | HECTD1 | GRCh38.p7 | 14:31106865 | TTAAACCAAGCTGGG[C/G]GTTTTGGTTTAGGGG | 25831 |
rs368704608 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111569 | TTTTTTTAAACACTA[G/T]TATGCATGAATTCAC | 25831 |
rs368718148 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125229 | CCCAGGCTAGAATGC[A/C]AATGGCACAATCGTG | 25831 |
rs368757424 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142488 | ACCCAGGCTGGAGTA[C/G]AGTGGTGCTATCTTG | 25831 |
rs368762482 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164634 | GTGCTTTGCCCATGG[C/G]CAAACATATAGGAAA | 25831 |
rs368777317 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134779 | TTTTGCTTCAATATT[-/T]CACAAGGAAGAGAGC | 25831 |
rs368812376 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161602 | AAAAAGAAAAAAAAG[A/G]AAGAAAGAAAGGAAA | 25831 |
rs368829363 | snp | A/G | 0.000335944 | 0.012956 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121539 | AAGAGATACATGTCT[A/G]ATTATTTGACCCATA | 25831 |
rs368836612 | snp | C/T | 0.000167986 | 0.00916323 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31174962 | TTCTACACAAATTTC[C/T]AAAGAAGAATCTTGA | 25831 |
rs368837991 | snp | C/T | 1.65666e-05 | 0.00287802 | missense | HECTD1 | GRCh38.p7 | 14:31113310 | AATAAGGGTCACTTG[C/T]AACTATATATAGAAT | 25831 |
rs368839384 | snp | C/T | 0.000159987 | 0.00894248 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129163 | GATCTCCGTTCCGTT[C/T]TGGTCGAACCCAAGC | 25831 |
rs368856327 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31113371 | ACAAGAGTTCTGTCC[A/G]TTGCCTGCTTTGGCC | 25831 |
rs368862659 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183636 | CTTTTAAGTCAAAAA[-/A]CTATTCCAATAATTT | 25831 |
rs368864658 | snp | C/T | 1.65726e-05 | 0.00287855 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139923 | GATCCTGGTGTATCA[C/T]ACAAATGGAGAGGTA | 25831 |
rs368903314 | snp | C/T | 0.000169985 | 0.00921758 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157329 | AAAAATAGAATTATA[C/T]GAAGCCAAATGAAGT | 25831 |
rs368911080 | snp | C/T | 3.31252e-05 | 0.00406958 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119832 | TCATCCCATGTTCTC[C/T]GGCGTCCTCCTTTAG | 25831 |
rs368943582 | snp | A/G | 0.000378668 | 0.0137547 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114107 | CCAATTATAAAGTCT[A/G]TGATATTTCACATGC | 25831 |
rs368947817 | snp | C/T | 0.000250914 | 0.0111979 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133474 | CAAAAGTAATTGTTT[C/T]AGTAAGTTAGAAAAG | 25831 |
rs368950940 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157413 | TTTATACACTCTGCT[-/A]AAAAAAATACACTTA | 25831 |
rs368955115 | snp | C/G | 0.000169985 | 0.00921758 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172137 | GCTGAAATTTTGAAG[C/G]AAAAAAAAAGAAACG | 25831 |
rs368964893 | snp | C/T | 0.000171985 | 0.00927163 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141898 | AGGCAGTTTTAAAAA[C/T]ATTTATTCTTTCTAC | 25831 |
rs368995830 | snp | A/G | 5.10078e-05 | 0.00504988 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105716 | ATGCAGCTACTACTA[A/G]TGGTGTTTAATTTTT | 25831 |
rs369003622 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185971 | GCACAATACCTAATA[A/G]TTCTGCTACATTTCT | 25831 |
rs369071455 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154451 | GACAGCCAAGTGCTA[C/T]CATGCCTGGCTCATT | 25831 |
rs369111594 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31121913 | TGAGAGTTCTGGATC[A/G]CATTGCCTATGCTTG | 25831 |
rs369116986 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165932 | CTCACTGCAACCTCC[A/G]CCTCATGGGTTCAAG | 25831 |
rs369118740 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201096 | AAACATATCAAAAAA[C/G]ATTTTTTTACCACTG | 25831 |
rs369149414 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144714 | GGCCATAATTTGCTG[A/G]CCCCCTACTCAATAC | 25831 |
rs369201933 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153683 | TAATTTTAGTGTATA[C/T]ATTTTAGTCTATGGT | 25831 |
rs369209427 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191166 | TACTTAAACATTTTA[G/T]GTTTTCGTAATTCAC | 25831 |
rs369291226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138019 | CTAATTAGCTTACTC[C/T]GCTAGAATATATTCT | 25831 |
rs369375532 | snp | C/T | 1.65688e-05 | 0.00287821 | missense | HECTD1 | GRCh38.p7 | 14:31103018 | ATTTGGACTTCTTCA[C/T]GGCTGAAGGAACTTA | 25831 |
rs369383258 | snp | A/C/T | 4.96841e-05 | 0.00498393 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129103 | ACAACAATTGGTTCA[A/C/T]GGACATCAGCTCCTG | 25831 |
rs369427495 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142965 | TTCAGCAGTACATAT[A/G]CCAAAACTGAAATGA | 25831 |
rs369433182 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118275 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 25831 |
rs369487877 | snp | C/G/T | 3.31598e-05 | 0.00407171 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121477 | GAGCGGGAGCCAGCT[C/G/T]GACGTTGCAGGGATG | 25831 |
rs369489655 | snp | A/C/G/T | 0.0016869 | 0.0289939 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107745 | GGTTAAACGTAAAGT[A/C/G/T]TGGGGTGTTTTTAAA | 25831 |
rs369491723 | snp | C/T | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127857 | GGCTGGTGGTTAAAG[C/T]GTTACTTAAAGATTG | 25831 |
rs369491780 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148685 | TTTAACAAATCAGTA[A/T]AAAAGACAAGAATAA | 25831 |
rs369548495 | snp | G/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208985 | CCAGTATTTTGGAAA[G/T]GACAAATTTGTACTT | 25831 |
rs369562416 | snp | A/C | 0.000169986 | 0.00921759 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157138 | TAAAGGAAATTAATG[A/C]TAAAGAGTTTTGAAA | 25831 |
rs369586606 | snp | C/T | 0.000566016 | 0.0168133 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157119 | TTTATTTCAGACTAC[C/T]AGCTAAAGGAAATTA | 25831 |
rs369592041 | snp | C/T | 0.000173985 | 0.00932535 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113212 | ATTAATTAATAAAAT[C/T]AATAAAAATATAAAC | 25831 |
rs369597603 | snp | A/G | 1.65644e-05 | 0.00287783 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105493 | TGCAAAAGAAAATTT[A/G]TCAGTATCTAGGAAT | 25831 |
rs369600969 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203933 | CCCCCGGTGTGTGAT[A/G]TTCCCCTTCCTGTGT | 25831 |
rs369613011 | snp | C/T | 0.000169986 | 0.00921759 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139991 | AATTAACGCAACTGC[C/T]GGTCGACTGCGAAGA | 25831 |
rs369712524 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114550 | AAACTCCTGGTTTCA[A/G]GCGATGCTCCTGCCT | 25831 |
rs369728567 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165480 | AATCCAGATGTGTCA[A/G]ATTTTCCTTACAGGT | 25831 |
rs369793503 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185975 | AATACCTAATAATTC[C/T]GCTACATTTCTTTCA | 25831 |
rs369794398 | snp | G/T | 0.00033295 | 0.0128982 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121355 | AAAAATATACATATG[G/T]TAGGGAAGATAAACA | 25831 |
rs369816298 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104710 | CAAGGTCTCCCTCTG[C/T]TGCCCAGGCTGGAGT | 25831 |
rs369821576 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136887 | AGTGCAGTGGCGCGA[C/T]CTCGGTTCACTGCAA | 25831 |
rs369825623 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144683 | AAAATGGGGAGCAGG[C/G]CAGATTTGGCTCCTG | 25831 |
rs369826223 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155536 | TTTTGCTAAAACACA[C/T]AAGCTGAATTTAATC | 25831 |
rs369827276 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160885 | TAGTTGCCCAGGCTG[G/T]TCTCAAACTCCTGGA | 25831 |
rs369840420 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195048 | ATCTGGTTTCTTAAA[A/G]ACAATAAATAACGCA | 25831 |
rs369921453 | snp | C/T | 0.000263581 | 0.011477 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173111 | AAACTGCCTATATGG[C/T]TATCTCACAACTTTC | 25831 |
rs370012398 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203218 | AGCCCATTCTTTCCA[C/T]CTCACTATGCCTCCC | 25831 |
rs370022170 | snp | G/T | 0.00020762 | 0.0101866 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127764 | AGTATCTAAATACTT[G/T]CATTTTAAATTACAA | 25831 |
rs370024702 | snp | A/C | 0.000285429 | 0.0119429 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100896 | TTCACTAGTATTTTT[A/C]AAGTCTCTGATGTCT | 25831 |
rs370080474 | snp | A/C/G | 0.000596774 | 0.0172636 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175163 | TAAAACAAATGTAAC[A/C/G]AAAGAATGCAAGCCT | 25831 |
rs370086268 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145018 | TTTTATAGACACTCG[C/T]ATTTACATATTTCAC | 25831 |
rs370103396 | snp | A/G | 1.66974e-05 | 0.00288936 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121533 | AATCCCAAGAGATAC[A/G]TGTCTAATTATTTGA | 25831 |
rs370152915 | in-del | -/A | 0.000237883 | 0.0109034 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112398 | TTATTCTAAAAACAT[-/A]AAAAAAAGGCTTCTT | 25831 |
rs370174970 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110775 | CTCAGCCTCCTAAAA[A/C]GCTGGAATTACGCCC | 25831 |
rs370184184 | snp | A/C | 6.69557e-05 | 0.00578562 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144813 | ATGACATACTTGTCT[A/C]TTTGTATGAAGTTCC | 25831 |
rs370218398 | snp | C/T | 1.65608e-05 | 0.00287752 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31109478 | GCCACGTGGAACTTT[C/T]ACTCTTTCATGCTTG | 25831 |
rs370279067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171488 | TATTCATTGCCAAGA[A/G]TAACAAATTGGAAAC | 25831 |
rs370313177 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187063 | AAAAACACCCAAAAA[A/C]CAGGCCTGGCGTGGT | 25831 |
rs370395677 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102020 | GATAAATTTATGTAA[C/T]GAAATAGTAAATGAA | 25831 |
rs370406504 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156663 | ATTTGCAACATTTCT[A/G]TATGTTTAAAATTGT | 25831 |
rs370449030 | in-del | -/A | 0.25728 | 0.249894 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106168 | TTATCAGCAAACATT[-/A]AAAAAAAAAGGCCTT | 25831 |
rs370482704 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196006 | TGTCTGTTTACAGGA[A/C]TTCATTTAACTTTTT | 25831 |
rs370563762 | snp | C/T | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121289 | TCCTCTCACCCCTTC[C/T]ACACTGCACATTTTT | 25831 |
rs370580620 | in-del | -/AG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102454 | TTTTTTTTGAGACAG[-/AG]TTTCACTCTTGTTGC | 25831 |
rs370581523 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136830 | ATTCTTTTTTTTTTT[-/C]TTTTTTTCTGAGACG | 25831 |
rs370593762 | snp | C/T | 3.35807e-05 | 0.00409747 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129403 | CCTTCTGCGCCCATA[C/T]GGTAAGAGTTTGAGC | 25831 |
rs370607462 | snp | A/C | 1.89213e-05 | 0.00307576 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135431 | TAGAATTCTTTTACC[A/C]AGTGAATATGGTCAC | 25831 |
rs370615404 | snp | A/G | 6.62471e-05 | 0.00575492 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173240 | GTGAGCGCTCCCCAG[A/G]ACTATCTAATCTCCG | 25831 |
rs370618690 | snp | C/T | 0.000902846 | 0.0212275 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109617 | AAATAGAAAAATATC[C/T]ATGAGCTGCAGCATA | 25831 |
rs370622387 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129581 | AGTCAATCAAGGTCT[A/G]CCCACTAAAATATAT | 25831 |
rs370622839 | snp | C/T | 3.31351e-05 | 0.00407019 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128703 | CGTGGCATTAGTCCG[C/T]GCTATGTTTGCCACT | 25831 |
rs370672958 | snp | A/C/G | 3.31753e-05 | 0.00407269 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173187 | ATCTATAAGTGCATC[A/C/G]GTATCTTTACTTCGA | 25831 |
rs370692797 | snp | A/T | 4.37963e-05 | 0.00467934 | missense | HECTD1 | GRCh38.p7 | 14:31114320 | TCTTTATCAGAATCC[A/T]TCATTTCTCTGTACA | 25831 |
rs370727683 | snp | C/T | 0.000163987 | 0.00905353 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127938 | CACTGGATGTTGACA[C/T]AGTCACTGTTGATGT | 25831 |
rs370738864 | snp | C/T | 0.000169986 | 0.00921759 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140012 | ACTGCGAAGAAATAA[C/T]TATTATTAAGAGGTT | 25831 |
rs370745759 | snp | A/G | 0.000101797 | 0.00713358 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177999 | AGAAAAATAAGTAAT[A/G]AGCCAATAAGTAATA | 25831 |
rs370774239 | snp | C/T | 0.000165785 | 0.00910303 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121480 | CGGGAGCCAGCTCGA[C/T]GTTGCAGGGATGGGC | 25831 |
rs370810482 | snp | A/G | 0.000167986 | 0.00916322 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169321 | CTGAAAAATAACAGT[A/G]GATGGCTTCAAAAGA | 25831 |
rs370850256 | snp | A/C | 4.96866e-05 | 0.00498406 | missense | HECTD1 | GRCh38.p7 | 14:31113385 | CATTGCCTGCTTTGG[A/C]CTGAGGTTGTTCTTT | 25831 |
rs370885122 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186148 | TTCATACACCACAAA[C/T]ATAAATCTCATCCAC | 25831 |
rs370932209 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111777 | TAATGTGCTCAATAT[A/G]CACATTAATTCTCTT | 25831 |
rs370957591 | snp | A/G | | | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122950 | GTCCTCCTGATTGTC[A/G]TCTTCATTCTCATCA | 25831 |
rs371004470 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203609 | CCCAGTCTCTTAAAA[A/G]TTACATCATACTATA | 25831 |
rs371005686 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198131 | AAAGAATAAACTAGA[A/T]GAAGCAAAATTATTA | 25831 |
rs371010804 | snp | A/G | 1.65622e-05 | 0.00287764 | missense | HECTD1 | GRCh38.p7 | 14:31113360 | TCTTCTACTCCACAA[A/G]AGTTCTGTCCATTGC | 25831 |
rs371012178 | snp | C/G | 4.96997e-05 | 0.00498472 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101035 | ATGCACACATGTATT[C/G]ACTGATGGATAGCTT | 25831 |
rs371019297 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139114 | ACCATGTGATTGATA[G/T]GAATAGTGAAGACTT | 25831 |
rs371025781 | snp | A/T | 0.000183277 | 0.00957104 | missense | HECTD1 | GRCh38.p7 | 14:31106907 | AATTCTGATTTTGAA[A/T]CCTCTTCAAAGCTTC | 25831 |
rs371026742 | snp | A/G | 3.3123e-05 | 0.00406945 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135098 | AATTATCACGACTTA[A/G]TATGTCTTCTAAGCG | 25831 |
rs371069986 | snp | A/C | 6.77851e-05 | 0.00582134 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141928 | CCAGTTGACTACAAT[A/C]TTGTTTCATATCCAA | 25831 |
rs371098732 | snp | A/G | 3.47192e-05 | 0.00416634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128585 | AGTGGAAAAAGCATC[A/G]GATTCCAGAAGGAAA | 25831 |
rs371100827 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187723 | GTGGTGTTAGATTAG[A/C]ACTAGAGATACTTGT | 25831 |
rs371115869 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163461 | CCAAAGAATTAGCTG[A/G]GCGTGGTGGTGCACA | 25831 |
rs371125720 | snp | C/T | 1.65671e-05 | 0.00287807 | missense | HECTD1 | GRCh38.p7 | 14:31109522 | GAAACTCTCCAGGGT[C/T]ATCTCGCCTAACACT | 25831 |
rs371199145 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145470 | TCAGGAGTTCAAGAC[C/T]AGCCTGGCCAACATG | 25831 |
rs371260055 | snp | C/T | 4.97071e-05 | 0.00498509 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31123029 | AATAGAGTACTGGCA[C/T]GGCAGCTATCAAGGA | 25831 |
rs371274199 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152409 | TACCTAGGCTAGGCT[A/C]GAATTCGTGGGCTCA | 25831 |
rs371330817 | snp | C/G | 1.65647e-05 | 0.00287786 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173381 | ATCTTTCATCACCCT[C/G]CAATGCACTTTCAAT | 25831 |
rs371404290 | snp | C/T | 2.88588e-05 | 0.00379849 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171819 | CTAATTTTTAAACCA[C/T]GTAAATGTTAAAAAT | 25831 |
rs371453340 | snp | A/G | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169415 | AGCTTTATCTAATGG[A/G]GTTTTCCCATCTTCA | 25831 |
rs371486435 | snp | A/C | 5.01567e-05 | 0.00500758 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113493 | AAAAATCCTATAGAA[A/C]CAATTAGAAAAACTG | 25831 |
rs371491130 | snp | C/T | 0.000346352 | 0.0131551 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129497 | GAAAGCAGATAGGAG[C/T]GTGTCAGACAGTAGC | 25831 |
rs371543287 | snp | C/T | 1.65636e-05 | 0.00287776 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205828 | CCACGTTGTCAGACA[C/T]CAAAAGCAGCATGCA | 25831 |
rs371580894 | snp | C/T | 8.32785e-05 | 0.00645231 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139842 | AGAAAAGTGTCACAC[C/T]GTTCCTAGATGCATT | 25831 |
rs371587125 | snp | A/C/T | 0.000301376 | 0.0122723 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149951 | AATATGAGAAAAAAA[A/C/T]CAAACTGTAGAAACT | 25831 |
rs371587991 | snp | A/G | 0.000155219 | 0.00880826 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173720 | CTCCTCAGTTAATCC[A/G]TGCTTGGCTAATGGA | 25831 |
rs371601558 | in-del | -/TAGA | 0.354019 | 0.227333 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188090 | ATATAGAGACAGCTG[-/TAGA]TAGATAGATAGATAG | 25831 |
rs371625297 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149443 | ACACTGTCTCCAAAA[-/C]AAAAAAAAAAAAAAA | 25831 |
rs371651945 | snp | A/G | 3.35233e-05 | 0.00409396 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107218 | TGACCTCTGCACATA[A/G]TATCCAGGAGGTTTC | 25831 |
rs371664492 | snp | C/G | 6.39407e-05 | 0.00565387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178305 | TTAAATTCTTAACAG[C/G]AAAATATTAACAAAA | 25831 |
rs371665100 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155507 | AGAAGAGCATAGTAT[C/T]ACCTCTATAGGACTT | 25831 |
rs371671173 | snp | C/T | 3.43814e-05 | 0.00414602 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144772 | CATCAAACTAAAATT[C/T]ACTACATATCATTAA | 25831 |
rs371684666 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208421 | CTTGTGGCTTGTGGT[C/T]ACAAGTATGTCTGTG | 25831 |
rs371688464 | snp | C/T | 1.66266e-05 | 0.00288323 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107146 | GAAATGAAACAGTTT[C/T]GTGATCCTTTCAAGC | 25831 |
rs371693440 | snp | A/G | 3.31225e-05 | 0.00406941 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122947 | TTGGTCCTCCTGATT[A/G]TCATCTTCATTCTCA | 25831 |
rs371696811 | snp | A/G | 4.5818e-05 | 0.00478611 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141998 | AAAAAATAATTTAAG[A/G]ATCTTACTGAAATTC | 25831 |
rs371713520 | in-del | -/GA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153793 | GGTAGTAAGGGTTGA[-/GA]CTAAGGGAGACTCAA | 25831 |
rs371735397 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164453 | TGTGCTCCCCCTTGT[C/T]TTTAATAATGCTAAA | 25831 |
rs371783240 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159941 | CACTGTGCCTGGCGC[A/C/T]GGTTTTTATTACTGG | 25831 |
rs371849959 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122661 | AGCCCTATACCCAGC[C/T]TAATTTCACACCCTT | 25831 |
rs371856031 | snp | A/G | 3.33845e-05 | 0.00408548 | missense | HECTD1 | GRCh38.p7 | 14:31116452 | AAGAGCTCTGAATGA[A/G]GGGTCCCTAAAAATT | 25831 |
rs371866688 | snp | C/T | 0.000167986 | 0.00916322 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173494 | CACTTTTTCTGAAGA[C/T]TAAAAAGCAAAGATT | 25831 |
rs371909515 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101955 | AATATGGATAAATAT[-/A]CCAAAGGGGATCTGA | 25831 |
rs371927909 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103437 | GTCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 25831 |
rs371938128 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130871 | AATAATCTCTGAAGA[A/G]CCAACATTTAACTAT | 25831 |
rs371961831 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206241 | AACTAGAAACCAGAG[C/T]TGTCTGTGTCAAAGA | 25831 |
rs371980433 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159227 | TTTAATGAAGGAATA[C/T]GCTTTATTACAAATT | 25831 |
rs371982394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188809 | GAAAAGAATTCCTTC[A/G]GCTCCCTTAATGAAC | 25831 |
rs371996446 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157713 | AGGCTGAGGGAGGCG[-/G]ATCGCTTGAGGTCAG | 25831 |
rs372035241 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31169637 | TGTAATCTCAGCACT[C/T]TGGGAGGCCGAGGTG | 25831 |
rs372062235 | snp | C/T | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31120974 | GCCTGGGCAATGAAG[C/T]GAAATCCTGTCTCAA | 25831 |
rs372070016 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31164999 | AAGTCTTGTGTAATT[-/A]AAAAAAAAAAAAAAA | 25831 |
rs372076268 | snp | C/G | 1.65655e-05 | 0.00287793 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128908 | GAACTAACATCAGGA[C/G]AACTAACACTGACAA | 25831 |
rs372160746 | snp | A/G | 5.04028e-05 | 0.00501985 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172007 | TTTATTAATATTTCT[A/G]TCCTTAATTTAAATA | 25831 |
rs372164112 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146252 | GACAGACATGCACAG[C/T]GCAGCAATAAATTTA | 25831 |
rs372167897 | in-del | -/CAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136038 | AAACAACAACAACAA[-/CAA]AAACAAAAAACAAAT | 25831 |
rs372199535 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169671 | GGGTCACCTGAGGAC[A/G]GAAGTTCAAGGCCAG | 25831 |
rs372225281 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31172521 | GAATCGCTCAAACCC[A/G]GGAGGCAGAGGACGC | 25831 |
rs372260103 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136890 | GCAGTGGCGCGATCT[C/T]GGTTCACTGCAAGCT | 25831 |
rs372282735 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135688 | TACCTACTTTTTTCC[-/TA]TCTCTTTAATGTGAA | 25831 |
rs372297580 | in-del | -/T | 0.00366153 | 0.0426305 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109643 | GCATACGTTAACAGC[-/T]GAATGTACTACTAAA | 25831 |
rs372353754 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118910 | AGGGAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAA]CTACCACAAATTTAT | 25831 |
rs372362959 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178807 | AAACTCTGTTTCAAA[A/G]AAAAAAAAAAAAAAA | 25831 |
rs372402879 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197484 | GTGGGATTTTCTGAC[C/G]AACAGTTTCTGCATA | 25831 |
rs372409445 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163667 | GTAATCCCAGCACTT[C/T]AGGAGGCAGAGGCAG | 25831 |
rs372452999 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149656 | ACCTGTAACTCCAGC[A/T]CGTTGGGAGGCCGAG | 25831 |
rs372456543 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104219 | AGAAATGATAAATGT[A/C]CAAGATGATGGATGT | 25831 |
rs372493012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124286 | ATGTCCCTTTTTTTT[C/T]CTCATCTTCCCTTTT | 25831 |
rs372506964 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203671 | AAATAACAGCTGTTA[C/T]GTTAGGATGGAAGGA | 25831 |
rs372519222 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195896 | TTTAATCACCTATGG[A/G]CCCCCTGGAGTCCCA | 25831 |
rs372543175 | snp | C/T | 0.000132477 | 0.00813761 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129051 | ACTGGAAGATGACCC[C/T]ACTTCTGTTTGAGGG | 25831 |
rs372550456 | snp | C/G/T | 1.66316e-05 | 0.00288367 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157136 | GCTAAAGGAAATTAA[C/G/T]GCTAAAGAGTTTTGA | 25831 |
rs372571826 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144983 | AATTTTTACAATTAA[C/T]AATTTTACCAAATCT | 25831 |
rs372658208 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31173902 | AGAAAGGCAACTGCA[A/G]CAAAGTGATTAAGCA | 25831 |
rs372671221 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126754 | GTGGCATGATCACAG[C/T]TCACTGGGGCCTTGA | 25831 |
rs372688325 | snp | C/T | 3.3432e-05 | 0.00408838 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171909 | ATAATGTAATGATGA[C/T]GACCTTTGACCTCTA | 25831 |
rs372695068 | snp | C/T | 0.000171136 | 0.00924872 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128039 | GCAAATCAGTACAAA[C/T]AGGTGAGATTGTAGA | 25831 |
rs372796210 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156769 | CAAAAACCATCAAAA[A/G]TTGAAACTAGATTTT | 25831 |
rs372796767 | snp | C/T | 3.31917e-05 | 0.00407367 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156972 | ATCTACTAAATCCCT[C/T]ATGATCTGCAAAGCC | 25831 |
rs372808503 | snp | C/T | 0.000189516 | 0.00973254 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157319 | CTTGAAAAGTAAAAA[C/T]AGAATTATATGAAGC | 25831 |
rs372826933 | snp | C/T | 0.000132668 | 0.00814348 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31112466 | CTGTCTAGTTTCAAA[C/T]GGTATTAGAAAAGGA | 25831 |
rs372828824 | snp | A/G | 1.6727e-05 | 0.00289193 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113256 | AACTGCTATAGAAAT[A/G]AAACAAGGCTTCTTA | 25831 |
rs372829512 | snp | A/G | 1.65622e-05 | 0.00287764 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129013 | TCACTTCCCGTTTCC[A/G]CTGTTAAGGTGCTGG | 25831 |
rs372847780 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143189 | GAGGCAAAGGCGGGC[A/G]GGTCACTTGAGGTCA | 25831 |
rs372882319 | snp | C/T | 1.6566e-05 | 0.00287797 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116373 | AACTTCACGAGTCGT[C/T]CCAAGACCTGTTACT | 25831 |
rs372928937 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153357 | AGATCACGACAGAGC[A/G]AGACTCCATCTCAAA | 25831 |
rs372935170 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190025 | ATGCTCTTAGAACCC[A/T]GTCACCATCCTGTGA | 25831 |
rs372955880 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196283 | CAGCCTCCCAAAGTA[C/T]CGGGATTACAAGCAT | 25831 |
rs372995633 | snp | A/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208997 | AAATGACAAATTTGT[A/G]CTTCAGATAGCTATC | 25831 |
rs373031560 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134182 | GGGGTGAAAACATCA[C/T]CTATTAATCCTAATG | 25831 |
rs373094446 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31113635 | ATAAATCAAGGCATT[C/G]TAAACCATTAAAATT | 25831 |
rs373132793 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186222 | CTCAATATCACTATC[A/T]CCATTTAGAAATATC | 25831 |
rs373205492 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108299 | TTTACTATGTTGGTC[C/T]GGCTGGTCTCAAACT | 25831 |
rs373214965 | snp | C/G/T | 3.31275e-05 | 0.00406975 | missense | HECTD1 | GRCh38.p7 | 14:31109504 | GCTTGAGACGACCAA[C/G/T]TCGAAACTCTCCAGG | 25831 |
rs373257200 | snp | A/G | 0.000167986 | 0.00916323 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175179 | AAAGAATGCAAGCCT[A/G]ATTTTCAAGAATCAC | 25831 |
rs373259028 | in-del | -/GA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141115 | TATTTTTAGTAGAGA[-/GA]TGGGTTTTTGCCATG | 25831 |
rs373337939 | snp | C/T | 0.000175984 | 0.00937877 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173114 | CTGCCTATATGGTTA[C/T]CTCACAACTTTCTTT | 25831 |
rs373355662 | snp | A/G/T | 3.39634e-05 | 0.00412074 | missense, synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144920 | AATGGTCATCGTATA[A/G/T]ATCTCGAGCCATAGT | 25831 |
rs373364026 | snp | G/T | 2.21109e-05 | 0.0033249 | missense | HECTD1 | GRCh38.p7 | 14:31114305 | TTTCCATTTTCCTTT[G/T]CTTTATCAGAATCCT | 25831 |
rs373461626 | snp | C/T | 6.62625e-05 | 0.00575559 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31105414 | TTGTTTCTGAATACC[C/T]GTATGCATACAAAAG | 25831 |
rs373472247 | snp | A/G | 0.000149151 | 0.00863442 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139962 | ATAGATTCTAGTACA[A/G]CTATTAACTTTCGAA | 25831 |
rs373484603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106579 | TTGCAAATCAGTGAC[A/G]ACAAAGAAACAAAAG | 25831 |
rs373511655 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114663 | AAACATAAGGCAAAG[C/T]AGCAGAAACCATATT | 25831 |
rs373531180 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166277 | AATGGTATGAAGCAA[-/A]CACCCATTCAGAAGA | 25831 |
rs373538980 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138866 | TTAGATAAAGGCAAA[-/A]TTCAAAGCAGAAGGC | 25831 |
rs373580571 | snp | C/G | 0.000169986 | 0.00921759 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140024 | TAATTATTATTAAGA[C/G]GTTTTGTATAACTAC | 25831 |
rs373624502 | snp | C/T | 4.9783e-05 | 0.00498889 | missense | HECTD1 | GRCh38.p7 | 14:31106662 | CTAAATCCTCTATGC[C/T]AAGTGGAGGCCCAGA | 25831 |
rs373690633 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191040 | AACTCCCTGCTACCC[A/G]GATGTTTCAGGAGCT | 25831 |
rs373736992 | snp | C/T | 5.00973e-05 | 0.00500461 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139995 | AACGCAACTGCTGGT[C/T]GACTGCGAAGAAATA | 25831 |
rs373841760 | snp | C/T | 0.000165986 | 0.00910854 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100907 | TTTTAAAGTCTCTGA[C/T]GTCTCCCATTGCACT | 25831 |
rs373848511 | snp | A/G | 0.000165588 | 0.0090976 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135021 | TGATGGTATCACCCA[A/G]AGACCCAGATCTATG | 25831 |
rs373849628 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112662 | TTGCCCAGGCTGGTG[C/T]GCAGTGGTACGATCT | 25831 |
rs373851698 | snp | A/C | 3.31246e-05 | 0.00406955 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127878 | TTAAAGATTGACCAA[A/C]TGATAAAACTGTTGT | 25831 |
rs373864462 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31150909 | GATCAGCCTGGGCAA[C/T]GTAGCGAGTCTGTCT | 25831 |
rs373868799 | snp | C/T | 0.000167986 | 0.00916323 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169351 | AAAGAATGTAGCTCT[C/T]ACCTGGAGACTGAAG | 25831 |
rs373875162 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198247 | CGGAAGAATAATGGC[A/T]AAGTACATACTTGAG | 25831 |
rs373881271 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120210 | CAACATGGTGAAACC[C/G]CATCTCTACTAAAAA | 25831 |
rs373893118 | snp | C/T | 0.000115931 | 0.00761264 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31113398 | GGCCTGAGGTTGTTC[C/T]TTTGTTAAATTAAGA | 25831 |
rs373929092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129864 | GAGATGAGGTCTTGC[A/G]TTGCCCATGCTAATC | 25831 |
rs373938352 | snp | A/G/T | 1.66918e-05 | 0.00288888 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175123 | CTGACTCACGAGTAC[A/G/T]TATCAGTTCTAATAC | 25831 |
rs373942320 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181801 | TAGCTGTTGAGTTAC[G/T]TTTTCAACAGTAACA | 25831 |
rs373963502 | snp | C/T | 4.97113e-05 | 0.00498529 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119861 | AGTTTCGTACTCTTC[C/T]TCTTCCTATCAAAAT | 25831 |
rs373986174 | snp | A/T | 2.63335e-05 | 0.0036285 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109624 | AAAATATCTATGAGC[A/T]GCAGCATACGTTAAC | 25831 |
rs374000916 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179456 | TAAAATAAAATAAAA[C/T]AAAATAAAATAAATA | 25831 |
rs374018492 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101895 | TATTCTGCAACAAAG[C/T]CAGCAAATCATAAAA | 25831 |
rs374023878 | snp | A/G | 3.31279e-05 | 0.00406975 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135113 | GTATGTCTTCTAAGC[A/G]GCCATAAGGTAGATT | 25831 |
rs374025669 | snp | A/C | 9.94365e-05 | 0.00705042 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128819 | CCAACAAAGAACTCA[A/C]TGACAGTCTGTTACT | 25831 |
rs374044577 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204090 | TCATCATTTTTTATG[G/T]CTGCATAGTATTCCA | 25831 |
rs374098213 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181995 | GCTTCCTGGGGTCAA[G/T]TAATTCTCCTGCCTC | 25831 |
rs374123832 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194866 | ATGCTTTTTTCACTT[A/G]AACTTGGGCCAAGAT | 25831 |
rs374146107 | in-del | -/A | 0.0700422 | 0.173537 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130478 | TTAACTTCCAAAAGC[-/A]AAAAAAAAAATTGTC | 25831 |
rs374170117 | snp | G/T | 5.0073e-05 | 0.0050034 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173454 | TGGGAAGAAAGATGT[G/T]TAATATATTAGCATT | 25831 |
rs374195471 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206393 | AAACTGATCTTCAGA[C/T]AAGGGTTAGATTCAG | 25831 |
rs374276358 | snp | C/T | 0.000231888 | 0.0107652 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105500 | GAAAATTTGTCAGTA[C/T]CTAGGAATATTTCAG | 25831 |
rs374285498 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146314 | TCAAAAAGGTGACAC[A/T]CTTTCTTGCTTCAGG | 25831 |
rs374313131 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115556 | TTGAGCTCAGAAGTT[C/T]GACACCAGCATGGGC | 25831 |
rs374320018 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165561 | GCCTACAAAAGCCAT[C/T]ATAGGTTATAAAAAG | 25831 |
rs374364491 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139322 | GATGGTGGAACTTCT[C/G]GGGGGGCTCTGCCCT | 25831 |
rs374376461 | snp | A/G | 1.65611e-05 | 0.00287755 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122889 | ACATCCTATCTTTGT[A/G]AAGAGAATGGGGTAC | 25831 |
rs374377603 | in-del | -/TA | 0.00119737 | 0.0244387 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100493 | TGCTCATTAATTCTC[-/TA]TGTTTTAAGGAAGCA | 25831 |
rs374383690 | snp | G/T | 0.000117605 | 0.00766736 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178254 | AGTGCGAGGAGGACA[G/T]CTGTAGTGAAAGAAA | 25831 |
rs374385337 | snp | A/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208819 | ACTGGAGCGGTTGAG[A/G]TGGGATGATCCCTCG | 25831 |
rs374393997 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186472 | CCGGGTGGATCACCT[A/G]AGGTCAGGAGTACGT | 25831 |
rs374471717 | snp | C/T | 3.31274e-05 | 0.00406972 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173390 | CACCCTGCAATGCAC[C/T]TTCAATTGAATCTGG | 25831 |
rs374474530 | snp | C/T | 0.000159987 | 0.00894248 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128631 | TGTGCTCATCACATT[C/T]CTCCCCAAAGTATTA | 25831 |
rs374480329 | snp | C/G | 0.000596219 | 0.0172556 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149961 | AAAAACCAAACTGTA[C/G]AAACTAGGAAAATAT | 25831 |
rs374500806 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187966 | TCACCATGTTGGCTA[C/G]GCTGGTCTCAAACTC | 25831 |
rs374511700 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112616 | TCATTCATTCGTTCA[-/T]TTTTTTTTTTTGAGA | 25831 |
rs374531535 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160611 | TTCTTAACTGTCTAA[C/T]AGGTAAAAATGATAC | 25831 |
rs374621317 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103132 | TCCAAGTTACGATTC[A/C]AAAATACCAAATTTC | 25831 |
rs374624832 | snp | A/G | 9.9486e-05 | 0.00705217 | missense | HECTD1 | GRCh38.p7 | 14:31106761 | TGCTTAAAATTTGGC[A/G]CCTCTTGATAGCAAG | 25831 |
rs374625344 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130195 | CATAGAAATTTTAGT[C/T]ACTAGTTCAAATAAA | 25831 |
rs374627534 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158084 | AAATCCACGTTCACT[A/G]CAACTATGGACTCAT | 25831 |
rs374628401 | snp | C/G | 1.70385e-05 | 0.00291873 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129422 | AAGAGTTTGAGCCAC[C/G]AGCATCCCAGGTGAC | 25831 |
rs374629888 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140805 | CACAATTATCTGAAT[-/A]AATTGTATAACTTGT | 25831 |
rs374643620 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127381 | TTTGAGAAGGAGTTT[C/T]GCTCTTGTTGCCCAG | 25831 |
rs374662211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102619 | ATTTTTAGTAGAAAC[A/G]AGGTTTCACCGTGTT | 25831 |
rs374729463 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166540 | AGGCAGTCGTGTGAT[A/G]TAATTACGATTTAAA | 25831 |
rs374758443 | snp | G/T | 0.000165986 | 0.00910854 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173222 | AATCTATAAGCTGCC[G/T]ATGTGAGCGCTCCCC | 25831 |
rs374762405 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153456 | CAAGTAATTCTCCTA[C/G]CTGAGCCTCCCCAAA | 25831 |
rs374764874 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183771 | AAAGTGCAGTGGCGC[A/G]ATCTTGGCTCACTGT | 25831 |
rs374779666 | snp | A/G | 2.29603e-05 | 0.00338816 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173813 | ATCTGAAACCTAACA[A/G]TGTGAAGAAAATGCC | 25831 |
rs374797182 | snp | C/T | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119782 | GATCAAAAGCAGGAA[C/T]CAATGCAGAAAACTG | 25831 |
rs374800589 | snp | C/G | 0.000169986 | 0.00921759 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139869 | CATTCAGCAATACTA[C/G]CTACTACATTTTTTA | 25831 |
rs374813199 | snp | A/G | 8.46518e-05 | 0.00650528 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103085 | CATCGTACATGTAAC[A/G]GAAACACAAAAAACA | 25831 |
rs374833621 | snp | G/T | 5.13685e-05 | 0.0050677 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133234 | GTGCTGAGCACCTAC[G/T]CACCATTGTGTAGTT | 25831 |
rs374838448 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103220 | AAAGAAAATGTGGTA[C/T]ATGTACACAATGGAA | 25831 |
rs374838817 | snp | C/G/T | 0.000333267 | 0.0129044 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169486 | AGAGAAGAAAAGCAT[C/G/T]TAATTTGAATATAAC | 25831 |
rs374859672 | snp | C/T | 0.000165986 | 0.00910855 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205751 | ATGGTTGAAAACAGA[C/T]GTCACTACAGTAACC | 25831 |
rs374874773 | snp | A/T | 9.93608e-05 | 0.00704773 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122968 | TTCATTCTCATCATC[A/T]TCTTCATCTGGCTCA | 25831 |
rs374883284 | snp | A/T | 0.00480189 | 0.0487636 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141999 | AAAAATAATTTAAGG[A/T]TCTTACTGAAATTCA | 25831 |
rs374885455 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193625 | TTATCTCCAAGAATT[G/T]CAGAATAAAAACTTA | 25831 |
rs374926613 | snp | A/C | 1.6775e-05 | 0.00289607 | missense | HECTD1 | GRCh38.p7 | 14:31107220 | ACCTCTGCACATAAT[A/C]TCCAGGAGGTTTCAA | 25831 |
rs374927070 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170598 | AACCTTCTTTGCTCA[C/T]TCAGTATTAGTCACC | 25831 |
rs374929518 | in-del | -/TAC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179427 | ACATCTCAAAATAAA[-/TAC]ATAAAATAAAATAAA | 25831 |
rs374938116 | snp | C/T | 1.71708e-05 | 0.00293003 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144774 | TCAAACTAAAATTCA[C/T]TACATATCATTAAAA | 25831 |
rs374962546 | snp | C/T | 6.62625e-05 | 0.00575559 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31103005 | TCCACAAAGAATCAT[C/T]TGGACTTCTTCATGG | 25831 |
rs374963988 | snp | A/G | 1.65718e-05 | 0.00287848 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135642 | AAAATATGAAAGACA[A/G]TCACCTTAATAATGC | 25831 |
rs374965096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201085 | CCTTTTAGTGTAAAC[A/G]TATCAAAAAAGATTT | 25831 |
rs374970283 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125843 | TGTCTTTAAAATTAC[A/T]CCCAATTTTTTTTTT | 25831 |
rs374975608 | snp | A/G | 3.31241e-05 | 0.00406952 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173263 | AATCTCCGGAGTCCT[A/G]GGATTCTGCCTGTAG | 25831 |
rs374994822 | snp | C/T | 5.09784e-05 | 0.00504842 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101348 | ACAAAAATATAGTTA[C/T]ATTGAGTTGACTGCA | 25831 |
rs375019469 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118251 | ACCTTGTGATCCACT[C/T]GCCTCAGCCTCCCAA | 25831 |
rs375039150 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162230 | GAGCAAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 25831 |
rs375059610 | snp | C/T | 4.96874e-05 | 0.0049841 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128959 | GACTCCCCAGGAGTA[C/T]GAACAGAACTATCAG | 25831 |
rs375072763 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114552 | ACTCCTGGTTTCAAG[C/T]GATGCTCCTGCCTTG | 25831 |
rs375089853 | snp | C/G/T | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121222 | ATTCTATATAGAATA[C/G/T]GAAACCCAACCAGTA | 25831 |
rs375111592 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131349 | TCATAGGGAGGTGCC[A/G]TACCTCACGGTTCAA | 25831 |
rs375121420 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137120 | AGCCACCACACCCGG[C/T]CTTTTTTTTTTTTTT | 25831 |
rs375144672 | snp | C/T | 1.67438e-05 | 0.00289338 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172023 | TCCTTAATTTAAATA[C/T]CAGCTTTTATTTATT | 25831 |
rs375154244 | snp | A/G | 3.35149e-05 | 0.00409345 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116461 | GAATGAGGGGTCCCT[A/G]AAAATTTGGAAGATG | 25831 |
rs375160435 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205707 | TTAAAATTCACTAGA[C/G]AAATTTCTACACAAA | 25831 |
rs375207515 | snp | A/C | 0.436692 | 0.166271 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196758 | GACTCCGTCTCAAAA[A/C]AAAAAAAAAAAAAAG | 25831 |
rs375225334 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185214 | GGGTGTGGTGGCAGG[C/T]GCCTGTAGTTCCAGC | 25831 |
rs375247631 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195164 | TGGTACAGCAGCTGA[A/G]AATTGTGGTTTTCCC | 25831 |
rs375291211 | snp | A/G | 0.000163987 | 0.00905353 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101053 | TGATGGATAGCTTGC[A/G]TCAGTAGCATCAACC | 25831 |
rs375293923 | in-del | -/TC | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111612 | CCAGCAGCTCAGACT[-/TC]TTTCCCTTGGTTTTC | 25831 |
rs375364474 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152942 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCTAG | 25831 |
rs375387446 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112756 | CTGGGATTATAGGCA[C/T]GTGCCACCGTGCCCA | 25831 |
rs375397811 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182143 | AAATGATCTACCCAT[C/T]TAGGCCTCCCAAAGT | 25831 |
rs375399990 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124391 | CATGGTATAGTATTC[A/G]TGCCTGCGGTAAGAG | 25831 |
rs375406141 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152211 | AGAGATCATACAAGT[A/G]GCCAGACATTTGCAT | 25831 |
rs375421611 | snp | A/G | 0.000163987 | 0.00905352 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136565 | TCCAGAGATTCAACT[A/G]TAGCCAAAGGTTCCA | 25831 |
rs375441933 | snp | A/C | 0.00016567 | 0.00909986 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31102939 | TGTATAACCCAGCTT[A/C]GGTTCAGTGTAATTG | 25831 |
rs375477314 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111949 | TCACACCACTGCACT[C/T]CTGCCTGGGCGACAG | 25831 |
rs375529442 | snp | A/G | 1.66974e-05 | 0.00288936 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121535 | TCCCAAGAGATACAT[A/G]TCTAATTATTTGACC | 25831 |
rs375535700 | snp | A/G | 0.000132679 | 0.00814382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136699 | AATACTCTGGAAAAC[A/G]TCTTGGTTTCTGTCT | 25831 |
rs375539366 | snp | C/T | 0.000215291 | 0.010373 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178185 | GGCTGTCACCTCTAA[C/T]ACATTGTCTGGAGCA | 25831 |
rs375615250 | in-del | -/CTA | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121074 | CATCTACTACCACTT[-/CTA]CTACTACTAAAACTA | 25831 |
rs375623416 | snp | A/C/T | 1.65842e-05 | 0.00287955 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133338 | ACGAGCTCCTGGAAC[A/C/T]ATGTATTTCAGAACC | 25831 |
rs375630331 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195962 | ACTTCTCTCTGCTGT[A/C/G]CACTGAAAAGAAGCA | 25831 |
rs375638908 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118011 | TTTAATACAGGTGTC[-/A]TTTTTTTGTTCGAGA | 25831 |
rs375645679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105080 | TGATCTCGGCTCACC[A/G]CAACCTCACCTCCCG | 25831 |
rs375664330 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114234 | TAGTTTTACTATCTT[G/T]CTTCTTTTAACTAAA | 25831 |
rs375672357 | snp | G/T | 3.31477e-05 | 0.00407096 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133564 | TTCGAATCCAGATAA[G/T]GAGAGGTAGTGTGTT | 25831 |
rs375677022 | snp | C/T | 0.000604715 | 0.0173779 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172173 | TTAAAGCCAATAAAA[C/T]ACTAAACTTTTCTAA | 25831 |
rs375710251 | snp | C/T | 6.85436e-05 | 0.00585381 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175148 | TAATACCTATAATAG[C/T]AAAACAAATGTAACG | 25831 |
rs375736283 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116815 | TTTGTATTTTTAGTA[C/G]AGACGGCAGGTTTCA | 25831 |
rs375751493 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205170 | TGGCTGTAAGGTCTA[C/T]CTAGTAAGAATTCTC | 25831 |
rs375786724 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144987 | TTTACAATTAATAAT[G/T]TTACCAAATCTTCAC | 25831 |
rs375814024 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124398 | TAGTATTCGTGCCTG[C/T]GGTAAGAGAAAAACC | 25831 |
rs375816307 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180257 | TAACTTAAAGGGTCC[A/G]GAAGAAAGAATACTG | 25831 |
rs375844740 | snp | A/G | 1.66604e-05 | 0.00288616 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123086 | TATGTCAACACAATT[A/G]AGAAAGCATAACAAA | 25831 |
rs375845619 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143410 | CAAAGCGAGACTCTG[C/T]GTCAAAAATAAATAA | 25831 |
rs375876128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119931 | TTGTTGCAAAAGCAA[C/T]GTGTTATTTAGAACT | 25831 |
rs375893669 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31168858 | CCATCCTGGCTAACA[A/C]GGTGAAACCCCGTCT | 25831 |
rs375937327 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110697 | TTGCCCAGGCTGGAG[C/T]GCAGTGGTGCAATCT | 25831 |
rs375938889 | snp | C/T | 3.32105e-05 | 0.00407482 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31112430 | CCTTGAGGCGCCAAA[C/T]GCTGTACATGTGAAA | 25831 |
rs375962732 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31121688 | TGCATTTTATACTAA[A/C]CTCCTTCATAAGAAG | 25831 |
rs375968357 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148850 | TTGTTACAATTTAAC[A/C]TATTCATTTATTTGT | 25831 |
rs375969911 | in-del | -/AG | 0.00159617 | 0.0282053 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100714 | CTTGTAAAGTAACAC[-/AG]TGTTCTGTGCTATAT | 25831 |
rs375977646 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114915 | TATCACTGTACTGAA[C/G/T]AGGCAACTGTAACAC | 25831 |
rs375988710 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145595 | ACAATCATTTGAACC[C/T]GGGAGGTGGAGGCTG | 25831 |
rs376050095 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105094 | CGCAACCTCACCTCC[C/T]GGGTTCAAGCAATTC | 25831 |
rs376124542 | snp | G/T | 2.12709e-05 | 0.00326114 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149168 | TCGGCTTTCTATAAA[G/T]ACAAAATACTTGTTT | 25831 |
rs376128114 | snp | C/T | 1.6722e-05 | 0.00289149 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113494 | AAAATCCTATAGAAA[C/T]AATTAGAAAAACTGG | 25831 |
rs376132311 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207723 | CATCGCGAACCGGGA[C/G]GGGGAGGGGAGGAGG | 25831 |
rs376151633 | snp | C/T | 0.000159987 | 0.00894249 | missense | HECTD1 | GRCh38.p7 | 14:31109506 | TTGAGACGACCAACT[C/T]GAAACTCTCCAGGGT | 25831 |
rs376193019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103824 | AATACAAAATTAGCC[A/G]GGTGTGGTGGTGCAT | 25831 |
rs376195357 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131348 | CTCATAGGGAGGTGC[C/T]ATACCTCACGGTTCA | 25831 |
rs376231602 | in-del | -/T | 0.0248432 | 0.108648 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146889 | AGCAAATAAGGTGTC[-/T]TTAAACAAAAACATA | 25831 |
rs376241084 | snp | C/T | 3.31214e-05 | 0.00406935 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129159 | TTCTGATCTCCGTTC[C/T]GTTTTGGTCGAACCC | 25831 |
rs376334029 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129271 | GTCTTGTCTGGACAG[C/T]TGTTTTTCACCAAGC | 25831 |
rs376339897 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168302 | TGAATAACTACCTTA[C/T]TGAAGGCAGCATAGT | 25831 |
rs376346747 | in-del | -/TATCA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31107785 | ATTCTTGTCAAAATT[-/TATCA]TATCTGATCCAGTAA | 25831 |
rs376407497 | snp | G/T | 0.000181722 | 0.00953038 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178286 | CATATTACATCTAGG[G/T]TTATTAAATTCTTAA | 25831 |
rs376462427 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163203 | TGACGTCGGAAGATC[A/G]CTTGAGCCCAGGAGT | 25831 |
rs376479630 | snp | C/T | 0.000159987 | 0.00894248 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173575 | AGAGCAGACTTACAA[C/T]TGTTGACACCTGATT | 25831 |
rs376511057 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131930 | TTATGAATTTTAGGT[C/G]GCTGTAAACCTGTTT | 25831 |
rs376547457 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175865 | GTGAAACTCTGTCTC[-/A]AAAAAAAAAAATAAT | 25831 |
rs376563190 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165847 | CAGTATTTCAGAGAG[C/T]GAAACCTTTTTTTTT | 25831 |
rs376582974 | snp | A/G | 1.66056e-05 | 0.00288141 | synonymous-codon, intron-variant | HECTD1 | GRCh38.p7 | 14:31113910 | CTGAGAACAATTTCT[A/G]TTTTTCCTAATACTT | 25831 |
rs376596778 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184969 | CTAAAAAAAATAACA[A/G]GTGTCATTTCCTAAT | 25831 |
rs376624148 | snp | C/T | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173230 | AGCTGCCGATGTGAG[C/T]GCTCCCCAGAACTAT | 25831 |
rs376637476 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202200 | CGAGACTCTGCCTCA[-/A]AAAAAAAAAAAAAAA | 25831 |
rs376639276 | snp | C/T | 0.000169986 | 0.00921759 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139974 | ACAGCTATTAACTTT[C/T]GAATTAACGCAACTG | 25831 |
rs376676379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152313 | TGGGATCATAGGGGT[A/G]AAGTTCCCTAGAGTA | 25831 |
rs376702330 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199962 | AGGCTTCACCTCCAA[C/T]TTCCATTTATACAAC | 25831 |
rs376703131 | in-del | -/TT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130349 | GCATACTGAACTCTT[-/TT]ATTAGAACTATCTGC | 25831 |
rs376711430 | snp | A/T | 3.31246e-05 | 0.00406955 | missense | HECTD1 | GRCh38.p7 | 14:31113372 | CAAGAGTTCTGTCCA[A/T]TGCCTGCTTTGGCCT | 25831 |
rs376739293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148309 | TAAACTAAGTATCAA[A/C]ATAATCTGAATTTAG | 25831 |
rs376751993 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147425 | ACAGGAAATAAAGAT[A/G]TGAACATCTTTATAT | 25831 |
rs376755167 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195756 | CAAACTCGCGACATC[A/G]GGTGATCCACCCGCC | 25831 |
rs376792673 | snp | A/G | 1.65605e-05 | 0.0028775 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135066 | CTTATCATCATTGCT[A/G]TGACAATTTAAAGCT | 25831 |
rs376813182 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110123 | TCTCCTGCCTCAGCC[C/T]CCCCAGTAGCTGGGA | 25831 |
rs376837224 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118804 | GAGGCGGAGGCAGGA[C/G]AATTGTTTGAACCTG | 25831 |
rs376837628 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198364 | CAAACATTTTTTCAA[A/C]ATTTAATCACGTATG | 25831 |
rs376852934 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193531 | TGTTCTTCATAAAAG[C/T]TGTTTTGGCAAGCAT | 25831 |
rs376890789 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118106 | GCCTCCCGGGTTCAA[A/G]CAATTTCTCCTGCCT | 25831 |
rs376897373 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142897 | ATCATGGCGAACACA[C/T]AGATGCACATACACA | 25831 |
rs376902746 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171367 | AGTGAGTCGCTACTG[C/T]GCCACTGCCCTCCAG | 25831 |
rs376937320 | snp | C/T | 0.000398589 | 0.0141115 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128048 | TACAAATAGGTGAGA[C/T]TGTAGAAACCTCAGA | 25831 |
rs376969740 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139328 | GGAACTTCTGGGGGG[G/T]CTCTGCCCTCATGAA | 25831 |
rs376972726 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179227 | AGTTCAAGAACAGAC[C/T]GGCCAACACAGTAAA | 25831 |
rs376976045 | in-del | -/GTGTAGAAT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31150228 | TTCATCTTCCTAAAT[-/GTGTAGAAT]TATTCAATTAAACAT | 25831 |
rs377010799 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171678 | GAACACATATATATA[C/T]ATTTGTTTTTATTGA | 25831 |
rs377055705 | snp | C/T | 3.3134e-05 | 0.00407012 | missense | HECTD1 | GRCh38.p7 | 14:31113307 | TTGAATAAGGGTCAC[C/T]TGCAACTATATATAG | 25831 |
rs377057083 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191505 | TGCACTCCAGCCTGG[A/G]CTGGAGATGGGGTTT | 25831 |
rs377060106 | in-del | -/A | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119302 | CCACAATCTAAAATA[-/A]GAGTTTTGTAAGGGA | 25831 |
rs377110842 | snp | A/G | 1.65605e-05 | 0.0028775 | missense | HECTD1 | GRCh38.p7 | 14:31109470 | AGTGACTCGCCACGT[A/G]GAACTTTTACTCTTT | 25831 |
rs377124634 | snp | A/C | 0.000169985 | 0.00921758 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107740 | TTGTGGGTTAAACGT[A/C]AAGTTTGGGGTGTTT | 25831 |
rs377130302 | snp | G/T | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127833 | CACTCTCACTGGAAG[G/T]TGATGTGAGGCTGGT | 25831 |
rs377165703 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162222 | TGAGTGACAGAGCAA[A/G]ACTGTCTCAAAAAAA | 25831 |
rs377173334 | snp | C/T | 0.000399873 | 0.0141342 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157118 | TTTTATTTCAGACTA[C/T]TAGCTAAAGGAAATT | 25831 |
rs377182098 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143820 | TCTATTTTATATAAC[C/T]TATGTAAAAATCAGA | 25831 |
rs377184731 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101999 | CCAGCAAAATAATTA[C/T]CTTGTGATAAATTTA | 25831 |
rs377187618 | snp | A/G/T | 0.000149392 | 0.0086415 | missense, synonymous-codon | HECTD1 | GRCh38.p7 | 14:31112495 | GACATTTGCTGGTTA[A/G/T]TTGTTCACACCAGTC | 25831 |
rs377189733 | snp | A/C/G | 6.62453e-05 | 0.0057549 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129021 | CGTTTCCGCTGTTAA[A/C/G]GTGCTGGTGCTTGCA | 25831 |
rs377201482 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191151 | CCTCATTTTTCCATA[C/T]ACTTAAACATTTTAT | 25831 |
rs377236853 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190124 | CAGCTAGAAGCCAGG[A/C]TCGACCACATGCAAC | 25831 |
rs377240234 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135825 | GAGATGGAGACCACC[C/T]TGGCCAACATGGTGA | 25831 |
rs377289892 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181999 | CCTGGGGTCAAGTAA[C/T]TCTCCTGCCTCAGCC | 25831 |
rs377311130 | snp | A/G | 0.000145106 | 0.00851658 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175180 | AAGAATGCAAGCCTG[A/G]TTTTCAAGAATCACA | 25831 |
rs377313402 | snp | C/G | 0.000159987 | 0.00894247 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129318 | TGTGCCTGAAACAGT[C/G]GATGAAACAGGTTTG | 25831 |
rs377381396 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186277 | TCAAAACAAAACTCC[C/T]GATGTGTGCCTCTAT | 25831 |
rs377420662 | snp | A/G | 1.73896e-05 | 0.00294865 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140038 | AGGTTTTGTATAACT[A/G]CATGTAAATGTTCAT | 25831 |
rs377423641 | snp | C/G | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178082 | CAACTACAACCAAAC[C/G]ATTACAAAGTGCTTT | 25831 |
rs377426150 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203447 | TAGTAAATCATATCT[A/G]ACTTAACTTTAGGTT | 25831 |
rs377428994 | snp | C/T | 3.31274e-05 | 0.00406972 | missense | HECTD1 | GRCh38.p7 | 14:31105435 | CATACAAAAGTCAAA[C/T]ATCAAATCCACATAT | 25831 |
rs377432052 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166559 | TTACGATTTAAAGAT[A/T]TAATTCTCAAGCCAA | 25831 |
rs377435037 | snp | C/T | 0.000333944 | 0.0129175 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121530 | AACAATCCCAAGAGA[C/T]ACATGTCTAATTATT | 25831 |
rs377481441 | snp | A/G | 0.000293384 | 0.0121081 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114371 | TTCAAGTTAATTCAT[A/G]TATAATTTGTGATTA | 25831 |
rs377484984 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117370 | GAACGAGACTCCATC[A/T]CAAAAAAAAATTTTT | 25831 |
rs377520083 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197977 | TTCCTGTGTTGACAT[A/G]CGCACTAATGATGCA | 25831 |
rs377566485 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31172146 | TGAAGGAAAAAAAAA[-/A]GAAACGTATTTTTAA | 25831 |
rs377587239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180991 | GTTAAAGTGTTAATA[C/T]TAAAGAAAAAACACA | 25831 |
rs377619162 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162524 | TACACACTACTCTGC[C/T]AGTTATCATAAAAAT | 25831 |
rs377632309 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114787 | AGCATTAGGTGATCT[A/G]GTGGTTGTGAAACAT | 25831 |
rs377632454 | snp | A/G | 5.0446e-05 | 0.005022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140002 | CTGCTGGTCGACTGC[A/G]AAGAAATAATTATTA | 25831 |
rs377639423 | snp | C/T | 1.65855e-05 | 0.00287967 | missense | HECTD1 | GRCh38.p7 | 14:31105616 | CACTTGGCTTGAGAT[C/T]CACAGCTGTAAAACC | 25831 |
rs377640342 | snp | C/T | 0.000149287 | 0.00863836 | missense, nc-transcript-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121405 | CCAATAGGTCGGCTC[C/T]CTGCTCCAGCAGGTA | 25831 |
rs377668706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151552 | GGCCCGCCACTACGC[C/T]GGACTAATTTTTTGT | 25831 |
rs377675318 | in-del | -/C | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206672 | GTAAATGCAATGGAC[-/C]AGCAGGTTACGGATC | 25831 |
rs377687158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132398 | GCTGATATTGCGCCA[C/T]TGCACTCCAGCCTGG | 25831 |
rs377717360 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31128280 | AAACAAAAGCTATAC[C/T]TATATGATGCTTTGG | 25831 |
rs377726775 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101674 | GCGCACGCCTGTAAT[C/T]CCAGCTACTTGGGAG | 25831 |
rs386776082 | multinucleotide-polymorphism | GA/TT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138263 | TAATAAACTTTAAAA[GA/TT]TGCAAAATAGTTTTT | 25831 |
rs386776083 | in-del | A/TT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146890 | GCAAATAAGGTGTCT[A/TT]AAACAAAAACATACT | 25831 |
rs386776084 | multinucleotide-polymorphism | CA/TG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179227 | AGTTCAAGAACAGAC[CA/TG]GCCAACACAGTAAAA | 25831 |
rs386776085 | in-del | CTTC/GA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189858 | TCTTTTTTAAAATGT[CTTC/GA]CTTTGATAGTCTTCC | 25831 |
rs397690491 | in-del | -/A | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155359 | CAAAAAAAAAAAAAA[-/A]GGAAAAGAGCAACTT | 25831 |
rs397695630 | in-del | -/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140945 | TTCTTTTTTTTTTTT[-/T]GTTATAGAGTCTCAC | 25831 |
rs397725366 | in-del | -/A | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132454 | AAAAAAAAAAAAAAA[-/A]TACATATATATACAC | 25831 |
rs397757411 | in-del | -/AG | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108117 | TATTTTTTGAGACAG[-/AG]TTTCACTCTTGTCGC | 25831 |
rs397760909 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192352 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAACA | 25831 |
rs397785105 | in-del | -/T | 0 | 0 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208937 | CTGGTTCTTTTTTTT[-/T]CTTTCTTTTTTACTA | 25831 |
rs397799763 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183087 | AAAGGTAAAAAAAAA[-/A]TCCCAGATTCCTAAA | 25831 |
rs397835632 | in-del | -/ATATAT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139054 | CAGATATATATATAT[-/ATATAT]CTGTATGGGGAGGAG | 25831 |
rs397852050 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163922 | TGTCTCAAAAAAAAA[-/A]TTTTTTTTTCAAAAG | 25831 |
rs397852415 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191563 | AAAAAAAAAAAAAAA[-/A]TTACTAACTGATTGA | 25831 |
rs397852443 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131043 | AAAAAAAAAAAAAAA[-/A]TAGAGTCAGTAATGA | 25831 |
rs397852789 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102446 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCAC | 25831 |
rs397852921 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154812 | GGATTCTACAATTAT[-/T]AACTCATATACCACC | 25831 |
rs397853501 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180025 | TACTAAAAATACAAA[-/A]TAATTAGCCGGGTAT | 25831 |
rs397949873 | in-del | -/GT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122400 | TGTGTGTGTGTGTGT[-/GT]CATTCTGTGGCTCAG | 25831 |
rs398024695 | in-del | -/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122641 | GTGTGGGACTACAGG[-/G]CATGAGCCCTATACC | 25831 |
rs398024696 | in-del | -/A | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161881 | GTCTCAAAAAAAAAA[-/A]GAAAAAGAAAAAGCC | 25831 |
rs398024697 | in-del | -/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188253 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 25831 |
rs527241048 | in-del | -/AT | 0.176219 | 0.238865 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139041 | ACATATTATATACAG[-/AT]ATATATATATATATA | 25831 |
rs527261650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156629 | TTGGATAGAGAGTAT[C/T]CTGATATTCTTTAAC | 25831 |
rs527301095 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100227 | AAAGAAAATACAACC[A/G]AAAGTAAAACTCGCT | 25831 |
rs527314449 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149939 | AATGGTAGCAAAAAT[A/G]TGAGAAAAAAACCAA | 25831 |
rs527352296 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163920 | TCTGTCTCAAAAAAA[A/C]AATTTTTTTTTCAAA | 25831 |
rs527375396 | in-del | -/A | 0.000250847 | 0.0111964 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105678 | TTAAACTGGGAGGAC[-/A]AAAAAAGATTAAATT | 25831 |
rs527391486 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205556 | AAATTAATATTCCTA[C/T]TAATTCCCATTCATT | 25831 |
rs527391524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198208 | ACTTAAAGGAAATGG[A/G]AATTAATTATAAAGC | 25831 |
rs527392068 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113581 | AGGGTTGGAATTTTT[A/T]AAAGTGCCTTCTTTT | 25831 |
rs527430739 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106090 | CAATCACGCTGTGTA[A/C]AAAAATATATATTAA | 25831 |
rs527478229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169542 | CTATGTAAACTAAAG[A/G]TTTTCCAGAATTACT | 25831 |
rs527502227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163439 | CAGAGTGAGCCCCTT[C/T]CCTCCCCCAAAGAAT | 25831 |
rs527605822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126251 | AATGATGTACATCAA[A/C]GCTGGTTGTCTGGTA | 25831 |
rs527695752 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157837 | AGCTACTCAGGAGCC[C/T]GAGGCGGAATAATCA | 25831 |
rs527795278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121250 | GTAGGGGAAGTTTCT[C/T]TGTGTAACTGTTTGG | 25831 |
rs527823681 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170979 | TACCAAATAACTTCA[C/T]GATTGGCAGATTACA | 25831 |
rs527843921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186269 | GAGTATATTCAAAAC[A/C]AAACTCCTGATGTGT | 25831 |
rs527844957 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181083 | AGTTGATAGTCCAAG[-/T]TATCAAATGACAAGA | 25831 |
rs527848532 | snp | A/G | 1.70208e-05 | 0.00291721 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177994 | GTCTGAGAAAAATAA[A/G]TAATGAGCCAATAAG | 25831 |
rs527858435 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157869 | TTGAACCTAGGAGAT[C/G]GTGCCACTGTACTCC | 25831 |
rs527915547 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170484 | ACTAACACCTTAAAC[C/T]TTTCATAATTTCATA | 25831 |
rs527921698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127134 | CCGCCACCACGCCCA[A/G]CTAATTTTTTTTATA | 25831 |
rs527944044 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171444 | ATATTTTATTGATGA[A/G]TACAAACAAGAGAAA | 25831 |
rs527990866 | in-del | -/A/AA | 0.444799 | 0.156695 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192335 | GCGAGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 25831 |
rs528021224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185734 | CCTGTTTAAAAAAAA[A/G]AAGAAGATAATTCAA | 25831 |
rs528031330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192685 | AAATTCCTTACAAGA[C/T]ATTCTACTGGCCGAG | 25831 |
rs528048592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117440 | AAACCACATATTCTG[A/G]GCCAATGACGTGTCA | 25831 |
rs528088994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175342 | CCAAGGTTGGCAGTT[C/T]GCTTGAGCCCAGAAG | 25831 |
rs528158600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131881 | TTCAACTCAGTATAA[C/T]AATAATAGTTGATAT | 25831 |
rs528160832 | in-del | -/AAAAAAAAA | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203604 | AGGCCCCAGTCTCTT[-/AAAAAAAAA]AAAAATTACATCATA | 25831 |
rs528161637 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157712 | GAGGCTGAGGGAGGC[-/G]GATCGCTTGAGGTCA | 25831 |
rs528186186 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124798 | TAATTTTTTTCATCA[C/T]CTAACAATAAATTTT | 25831 |
rs528195766 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124120 | TACCCTTTAACACTT[G/T]TAAGGAGCCACCTGC | 25831 |
rs528226996 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174564 | AAAAAATAATAAAAA[A/T]AAAAAATACCGTCTT | 25831 |
rs528315179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182350 | GTATGCCAACACGCC[A/G]AGCTAGTTTTTAAAA | 25831 |
rs528316343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131181 | AAAACTAAATTTCTA[C/G]ATTTGTCAGATTAGC | 25831 |
rs528321727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139262 | AATGTTTGTGTCCCC[A/G]CAAAATTCATGTGTT | 25831 |
rs528394625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138528 | TGAGACTTATCTCCA[A/G]CTCATCCACTTACCA | 25831 |
rs528396575 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197505 | TTTCTGCATAATCTA[C/G]GACCATATTAGAAAT | 25831 |
rs528401668 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146784 | GTTGAACCTGGAAGG[C/T]GGAGGTTGCAGGGAG | 25831 |
rs528415679 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188146 | AGATAGATAGATAGA[C/T]AGACAGATAAAAGCT | 25831 |
rs528425075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195588 | CACAGTGGTGCAATT[C/T]CGGCTCACTGCAACC | 25831 |
rs528433015 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183993 | GATTACAGGTGTGAG[A/C]CACCACACCTTGCCC | 25831 |
rs528436278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188524 | CAGGCGTGAGAAACC[A/G]CGCCCGGCCTTGTTA | 25831 |
rs528452043 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167595 | AAACCCTTTGGTAGT[C/T]TGGATCAGAGTACTG | 25831 |
rs528525541 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131556 | AGGAATGTCACAGTG[C/T]AAGATGCTGCTAGTA | 25831 |
rs528581084 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140893 | CAACCCAGCTTTAGC[A/C]ATTAGCTACTAATGG | 25831 |
rs528586286 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197940 | CAAAACAATTGCCCT[C/T]TCTCTTCTTGAATCA | 25831 |
rs528669166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203904 | CCCTCCCCCCTCCCC[A/C]TACCCCACAACAGCC | 25831 |
rs528692583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147753 | AGAGCGAAACCGAGT[C/T]TCAAAAAAAACATTA | 25831 |
rs528772182 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31210053 | TTTGAGACGGAGTCT[C/T]GTTCTGTTGCCCAGG | 25831 |
rs528781358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111813 | GAATCTTGCCCTTGT[C/T]TGTTTACAACAATGC | 25831 |
rs528802375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203481 | TTCCTTAAAATTACA[C/T]TATAAAGCCAGGTGT | 25831 |
rs528817240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112154 | TAGATTTGCATATAC[A/G]TGGCCAAAGGAACAA | 25831 |
rs528839781 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202074 | GTGGATCACAAGGTC[-/A]AGGAGATTGAGACCA | 25831 |
rs528866148 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177796 | ATAAGATTTCTTTTC[A/G]CAAGTCCCATGGAAC | 25831 |
rs528893675 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168770 | TTGGTCAGCCGGGAG[C/G]AGTGGCTCACGCCTG | 25831 |
rs528895567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161504 | CTGTGCCATGGAATT[C/G]AAGGTTGCAGTGAGC | 25831 |
rs528899038 | in-del | -/AAT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177510 | AACTGTCTCAAAAAC[-/AAT]AATAATAATAATAAT | 25831 |
rs528908263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162208 | ACTGCACTCCAACCT[C/G]AGTGACAGAGCAAGA | 25831 |
rs528923622 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124023 | CAAGTCAGAATTAAA[C/T]TGCAACATTTTTAAC | 25831 |
rs528930747 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196038 | TTTTTTTTTGAGACG[A/G]AGTCTCACTCTGTCT | 25831 |
rs528984005 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118284 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC | 25831 |
rs529079828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175496 | ACTTGAGCCCAGGAG[A/G]TCAAGGCTGCAGTGA | 25831 |
rs529132558 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191816 | CCAGCCTGACCAACA[C/T]GGAGAAAACCCCGTC | 25831 |
rs529140458 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127011 | GAGTCTTGCTTTGTC[A/G]CCCAGGCTGAAGTGC | 25831 |
rs529158619 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157073 | ATGCAGTAATTTGCA[A/C]AACATGATTTACTGA | 25831 |
rs529188055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131951 | AAACCTGTTTTGATT[A/G]CAATGATTTGCAATT | 25831 |
rs529216679 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160113 | CAGTAACCTTTTTAT[A/G]TACTTTAAAAACATA | 25831 |
rs529230102 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135705 | TCTCTTTAATGTGAA[C/T]TGTTTTCTTTTATTA | 25831 |
rs529261222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177000 | ACAAATAGTTCCAAA[A/G]AAGTATGGATCTAGC | 25831 |
rs529285241 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135063 | ATTCTTATCATCATT[A/G]CTATGACAATTTAAA | 25831 |
rs529309182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126459 | TTTGCAAGAATCATG[C/T]ATTACCTAACTAAGG | 25831 |
rs529311388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141405 | GTGTTCAAATTTTCA[A/G]CTATCTTAAACAGGC | 25831 |
rs529311760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133739 | AAGAAATTCAAGATG[C/G]GAAAGATTTTTTATA | 25831 |
rs529363882 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132209 | TTGGGAGGCCGAGGT[A/G]GGTGGATCACCTGAG | 25831 |
rs529452729 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197978 | TCCTGTGTTGACATG[C/T]GCACTAATGATGCAA | 25831 |
rs529454526 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148423 | AAAAATATCCTAGTA[A/T]CATTAATAATCTCAA | 25831 |
rs529463153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197930 | CACTAGTATTCAAAA[C/T]AATTGCCCTTTCTCT | 25831 |
rs529465425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190626 | CTCTGTAGGCCAGAC[C/T]GGAGTAGGATGGCAC | 25831 |
rs529516951 | snp | G/T | 1.65674e-05 | 0.00287809 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148997 | AGCTTGCTGACCATC[G/T]GAATTATGAATAGCA | 25831 |
rs529529434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191353 | CAACACAGCAAAACT[C/T]TGTCTCTACAATAAA | 25831 |
rs529533051 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112712 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCCTA | 25831 |
rs529535818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155301 | GGTGAGCCGAGATCA[C/T]GCCATTGCACTCCAG | 25831 |
rs529539879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204058 | GCTCCATCCATGTCC[C/T]TACAAAGGACATGAA | 25831 |
rs529582307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104653 | TCAAGTAATCTAGAA[C/T]GTATGCAACCTATGT | 25831 |
rs529617976 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195596 | TGCAATTTCGGCTCA[C/T]TGCAACCTCCGCCTC | 25831 |
rs529619246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153163 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCACGAGG | 25831 |
rs529663190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172711 | TAAATACACAACTAA[A/G]TAAGGTAGTAGTTGC | 25831 |
rs529679275 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181496 | AGTGTGCACCTGTGG[G/T]CCCAGCTACTCGGGA | 25831 |
rs529696077 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182966 | ACTCCTTTCATTTAC[A/G]TGGTATTTCCTGTAA | 25831 |
rs529708174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145121 | ACCTATGTATGTTCT[C/G]GGTCTGATGAAATTT | 25831 |
rs529721694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137374 | ACCTCAGGTGACCCG[C/G]CTACCTTGGTCTCCC | 25831 |
rs529738198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130162 | TTGGGCTAACCTCTC[A/C]AAATATTCATATATT | 25831 |
rs529768866 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185404 | GGAATTTCATAGCAT[A/C]ATTTTCAGAGAAACC | 25831 |
rs529797299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194059 | AATATTACTTAGCAA[C/G]TAAAGAGAATGAACT | 25831 |
rs529800901 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137720 | ACTCCAGCCTGTGCA[A/C]CAGAGCTAGACCCAG | 25831 |
rs529860009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101921 | TAAAAACACAGGATG[C/T]ACTTGCAAAATCATT | 25831 |
rs529865297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144332 | ACTTATCAGAACATC[A/G]ATTATCATGACAATA | 25831 |
rs529885871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200722 | GGAGGTGGAGGTTGC[A/C]GTGAGCTCAGATCAC | 25831 |
rs529927808 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115243 | AAAAAAACTGAAGGG[A/C/T]GGGAGAATACCGTTA | 25831 |
rs529982561 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207256 | AGCGGGGAAGTCGGC[A/G]GCAGCCTGGCCGACC | 25831 |
rs529989949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195732 | TCACCATATTGGCCA[C/G]ACTGGTCTCAAACTC | 25831 |
rs530007406 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103830 | AAATTAGCCGGGTGT[C/G]GTGGTGCATGCCTAT | 25831 |
rs530108101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146098 | TTGGTTGGTTAATAC[A/G]ACATATTAGATATTC | 25831 |
rs530114920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201730 | TGCCAGGCTGGTCTT[G/T]AACTCCTGACCTCAA | 25831 |
rs530173377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194996 | CAGGCACTTCATTTT[A/T]AAAAAATGAAATATT | 25831 |
rs530178364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202394 | CCATTGCAGAGGCCA[C/G]TGTTTCTACCACACC | 25831 |
rs530214522 | snp | A/T | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119427 | TGATCCAGTAGAAAA[A/T]ACAGTAAAAATTTCC | 25831 |
rs530231491 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166865 | CTAAAAAAAATTTTT[A/T]AAAAAATGTATATAA | 25831 |
rs530238586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103410 | AGCCGGGCGTGGTGG[C/T]GGCTGCCTGTAGTCC | 25831 |
rs530268216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116761 | TCAGCCTCCCGAGTA[C/G]CTGGGATTATAGGTG | 25831 |
rs530308721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130868 | TGAAATAATCTCTGA[A/G]GAACCAACATTTAAC | 25831 |
rs530348409 | in-del | -/ACAT | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156520 | AAAAAAAAAGTACAC[-/ACAT]ACACACACACACACA | 25831 |
rs530361249 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173677 | GTCCTGAAACAGTAC[C/T]ACCAGCAGCAGCCAT | 25831 |
rs530363227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166048 | ACAGGGTTTCGCCAC[A/G]TTAGCCAGGCTGGTC | 25831 |
rs530437336 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160801 | TCAGCCTCTCGAGTA[C/G]CCAGGACTACAGGTA | 25831 |
rs530463475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131687 | ATGCAATTGCTTCAG[C/T]TGACTCCATCCTGAG | 25831 |
rs530506767 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182213 | TTTTTTTTTTCCAGA[C/T]AGGGTCTTGCTCTGT | 25831 |
rs530507461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138443 | CACATTCCTGGCCTT[C/T]CTCTCTTTGGATCTT | 25831 |
rs530519223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173904 | AAAGGCAACTGCAGC[A/G]AAGTGATTAAGCATG | 25831 |
rs530536173 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117016 | ATACATGTGTATGAT[A/G]GAGAGCTCTCTCATT | 25831 |
rs530586199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103309 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAT | 25831 |
rs530716461 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185653 | GATCACATGAGCCCA[C/G]GGAGGTCCAGGCTGC | 25831 |
rs530736775 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183659 | AATAATTTTGTGTCA[A/T]CACTACTCAACTTAA | 25831 |
rs530738213 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188380 | AGCTAGGATTACAGG[C/T]GCCTGCCACCACACC | 25831 |
rs530766597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189886 | TTCCCTATGAGAGGG[C/G]CTGAGTTCTTTCCTC | 25831 |
rs530799064 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194970 | GATATTTTATAAAAT[A/G]GTCTGTAAATCAGGC | 25831 |
rs530808240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152509 | CCCAATATTCTTTAC[A/G]AAAGACCACAAAGCC | 25831 |
rs530812298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200762 | CTCCAGCATGGGTGA[C/G]AGAGCAAGACTCTTG | 25831 |
rs530827191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190376 | TCCACAAGTATTGTG[C/G]TGCGGCTGGAAATCA | 25831 |
rs530845690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145229 | CAAACCCAGCATAAC[G/T]CTAATGCAACAGAAA | 25831 |
rs530885611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154493 | TGTAGAGATGGGGTT[C/T]CACAATGTTGGCCAG | 25831 |
rs530917974 | in-del | -/AC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160394 | TTTATTTTTGTGTAA[-/AC]AGTTTCTTCATATTC | 25831 |
rs531007231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147068 | TGTAATCCCACTACT[C/T]TGGGAGGCCGAGGCA | 25831 |
rs531075690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167529 | CAAACATTGTAAAGG[A/G]GCAAGAGAGAAAAAG | 25831 |
rs531089927 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124041 | CAACATTTTTAACCT[C/T]AGTAACAGAAAAAAA | 25831 |
rs531097150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202593 | ATATGCACATCATCT[G/T]GCTTTTTTTGCCTGC | 25831 |
rs531101476 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31210029 | TTTTGTTGTTTTTTT[G/T]TTTTTTTTTTTGAGA | 25831 |
rs531114016 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103541 | GCCTGAGACTCCGTC[C/T]CAAAAAAAAAAAAGA | 25831 |
rs531168318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153946 | TGGTGGTCTTAGCAC[C/T]TTTGTTGAAAATCAA | 25831 |
rs531325781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150779 | GTGAAGTGTGTAACA[C/G]AATCACCAAAGAAGC | 25831 |
rs531335573 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100331 | AAGACTTTGATCTTC[A/C]TAGTATGGCATTTAG | 25831 |
rs531344269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192143 | CTCAGGTCAGGAGTT[A/C]AAGATCAGCCTGGAC | 25831 |
rs531360557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143214 | AGGTCAGGAGTGCGA[A/G]ACCAGCCTGGCCAAC | 25831 |
rs531370892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205703 | CGTGTTAAAATTCAC[C/T]AGAGAAATTTCTACA | 25831 |
rs531386872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157679 | CAGCGGCTCACGCGT[A/G]TAATCCCTGCATTTT | 25831 |
rs531413477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206621 | CTATTCTTAAAAGTT[A/T]AAAAAATAAAAAAAT | 25831 |
rs531444051 | snp | C/T | 0.00129566 | 0.0254195 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156805 | AAAAAAAAAAAAAAA[C/T]TCTTCCTGATACCTC | 25831 |
rs531467148 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170001 | ATGTCACCTTCTCCA[A/T]CAAACTCTGCCTCCC | 25831 |
rs531469954 | in-del | -/TAAC | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138352 | TTTCTGTATAAATCT[-/TAAC]TAATTCCTATAAAAA | 25831 |
rs531475873 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199747 | AAAAAAAACAACTTC[C/T]CAGTTTCATTCTGAA | 25831 |
rs531487010 | snp | C/T | 1.65776e-05 | 0.00287898 | synonymous-codon, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119711 | AAAACATTCTGTACC[C/T]GGGGGTGGTATTTCT | 25831 |
rs531488743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114192 | GTTAGTCATTATTCC[C/G]TTCAACGTTCAACTG | 25831 |
rs531525918 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190543 | CAAAGAGGTAATACT[G/T]TATCTAAAGATTGAT | 25831 |
rs531554095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115979 | GATAGTTAGTACTCA[C/T]ACACGATCTTAGACA | 25831 |
rs531609254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126949 | GTGCTGGGATTATAG[A/G]CGCAAGCCACCACTT | 25831 |
rs531644448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151934 | GAAAGCAAACAAAGC[A/G]AGTCTCTTAGAACCA | 25831 |
rs531653318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120310 | AATCGCTTGAACCTG[C/G]GAGGCGGAGGTTGCA | 25831 |
rs531657149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113645 | GCATTCTAAACCATT[A/T]AAATTCCCAAATAAA | 25831 |
rs531713622 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-5-prime, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207396 | AGGCTCTTACTCGGG[C/T]TTGTCGTTCCAAACC | 25831 |
rs531801259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171069 | TCTCTAACTGTAAAA[A/G]TAACTCCCCAAAGTC | 25831 |
rs531804515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165462 | GTGATCTTGATCAAC[A/G]GAAATCCAGATGTGT | 25831 |
rs531828743 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134213 | TTAAGAAGCTCCTCT[A/C]ATACCATATCAAATG | 25831 |
rs531851468 | snp | A/C | 3.32369e-05 | 0.00407644 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121367 | ATGGTAGGGAAGATA[A/C]ACATGAAGATATTAC | 25831 |
rs531888608 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155263 | GGCATGAGAGTCGCT[G/T]TAACCCAGAAGGTGG | 25831 |
rs531919422 | in-del | -/A | 0.0260105 | 0.111035 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108505 | CTACAGCATATGGTT[-/A]AAAAAAAAAGATTAT | 25831 |
rs531922706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179824 | ATGGAATAATTTATC[C/T]TCCTATTCTTAGTGT | 25831 |
rs531937133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179006 | ACTGCTCAATTCATA[C/T]TTTTCAGAAAGAAGC | 25831 |
rs531942706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187228 | GGGGCAGTGGCTTGT[A/G]CCTGTAGTCCCAGCT | 25831 |
rs531997717 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141143 | ATGTTGGCCAGGCTG[A/G]TCTCGAACTCCTGAC | 25831 |
rs532001065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179923 | GCTCACGCCTGTAAT[C/T]CTTGCACTTTGGGAG | 25831 |
rs532047465 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200007 | CTCCACTGAGATGTC[C/T]CAAAAGTACCTCATA | 25831 |
rs532061190 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145574 | TACTCAGGAGACTGA[A/G]GCGGGACAATCATTT | 25831 |
rs532077840 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143341 | ATCACTTGAGCCCAG[A/G]AGGCAGAGGCTGCAG | 25831 |
rs532177289 | in-del | -/A | 4.97991e-05 | 0.0049897 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148807 | CTGAACCTTGGGGGG[-/A]AAAAAAAGAATATTC | 25831 |
rs532180500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199840 | TTAAGAGCTTAAGGA[A/T]GTCCTGAGACCATAG | 25831 |
rs532216604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158300 | TCGCTCTGTTGTCTC[A/G]GCTGGAGTGTAGTGG | 25831 |
rs532263677 | in-del | -/AAG | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108675 | TTAAAAAAAAAAAAA[-/AAG]AAGAAGAAGAACATA | 25831 |
rs532292895 | in-del | -/CTTT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127523 | CTCCCGGATAATTTT[-/CTTT]TGTATTTTTAGTAGA | 25831 |
rs532317404 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108086 | CCAAAGCCTAGACTC[C/T]TCCACTTTTTAATTT | 25831 |
rs532343598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102726 | TGAGCCACCGCGCCC[A/G]GCCTGCTGTCAGTTG | 25831 |
rs532353298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108688 | AAAAGAAGAAGAAGA[A/T]CATAAGGGTAGGAGG | 25831 |
rs532380548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103371 | CACAGTGAAACCCCG[C/T]CTCTACTAAATATAC | 25831 |
rs532382430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159739 | CCGACTCCCAGGTTC[A/G]AGTGATTCTCGTGCC | 25831 |
rs532469119 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114720 | ATTATTACAAAGAAA[A/G]CATGTATCAAATCTA | 25831 |
rs532479793 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208562 | AACAAAAAGAAAAAT[G/T]AATACGACATGATAG | 25831 |
rs532500385 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131238 | ACTCTGAGATTTCTA[A/G]GCTAGGTGATTTTTT | 25831 |
rs532530430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116727 | CCTCCGCCTCCCAGG[C/T]TCAAGCAATTCTCCT | 25831 |
rs532566961 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115728 | ATCGCACCACTGCAC[C/T]CCACTGCACTCCATC | 25831 |
rs532582626 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153185 | ATCACGAGGTCAGGA[A/G]ATCGAGACCATCCTG | 25831 |
rs532620553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159331 | GTTTTGTTGTTTTTA[A/G]TTTAATTTAATTTAT | 25831 |
rs532657182 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155445 | TTATCATAACCAACA[A/G]GGTAAACAGACACAA | 25831 |
rs532674214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110258 | TCCACCCGCCTCAGC[C/T]TCCCAAAGTGCTATG | 25831 |
rs532677086 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137697 | GCGAGCTGAGATCAC[A/G]ACACTGCACTCCAGC | 25831 |
rs532697532 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100258 | GTAAGTGTGCCTTGC[A/G]CTTAGACCAGGTTTT | 25831 |
rs532700244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180672 | CTGGTATTGAACTCC[C/T]GGCCTCAAGTGATCT | 25831 |
rs532736857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105248 | TCAGGTGATCCTCCC[A/G]CCTCAGCCTCCCAAA | 25831 |
rs532741181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204646 | AATAAAAATAAATTT[C/T]AAAAAATCTACTTTA | 25831 |
rs532772027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105971 | CTTTCTATATTTTAC[C/T]TCTAACTTATGGCAC | 25831 |
rs532847409 | snp | A/G | | | missense | HECTD1 | GRCh38.p7 | 14:31113309 | GAATAAGGGTCACTT[A/G]CAACTATATATAGAA | 25831 |
rs532875201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204147 | ATCCAGTCTATCATC[G/T]ATCGACATTTGGGTT | 25831 |
rs532882209 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118825 | TTTGAACCTGGGAGG[C/T]GGAGGGTGCAGTGAG | 25831 |
rs532889461 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130709 | AAGTTCATATGTTTA[C/T]GATAGCACTCAGAGG | 25831 |
rs532911860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113544 | GAAAAACAGTGTATC[A/G]TTGTATCAATACCAC | 25831 |
rs532937605 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163236 | GAGACCAGTCTGGGC[A/T]ACACAGCAAGACTTC | 25831 |
rs532987505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168898 | ATACAAAAAAAATTA[A/G]CTGGGCACGGTGGCG | 25831 |
rs533014150 | snp | C/T | 6.67635e-05 | 0.00577731 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169491 | AGAAAAGCATTTAAT[C/T]TGAATATAACAATAC | 25831 |
rs533047626 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171325 | GCTGAGGCACGAGAT[C/G]GTTTGAACACAGGAA | 25831 |
rs533082349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119592 | AAATTTTTTATAACC[C/T]GCATACACAAAACTA | 25831 |
rs533086688 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127358 | GTTTGTTGTTTTCTG[-/T]TTTTTTTTTTGAGAA | 25831 |
rs533090829 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174716 | AATAAACATATATCA[C/G]ACTTATAATCTTAAA | 25831 |
rs533117727 | snp | C/G/T | 1.65633e-05 | 0.00287774 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127834 | ACTCTCACTGGAAGT[C/G/T]GATGTGAGGCTGGTG | 25831 |
rs533118588 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125456 | AGGATTACAGGCGTG[A/C]GCCACAGCGCCCGGC | 25831 |
rs533239121 | snp | A/G | 6.62943e-05 | 0.00575698 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135145 | CTTCCTTCTGATGAC[A/G]TTACTACTACAAGTC | 25831 |
rs533239874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140794 | TTTGAAATTAACACA[A/G]TTATCTGAATAAATT | 25831 |
rs533277456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125101 | GTGAGCCACTGTGCC[C/T]GGCCAACAATAAATT | 25831 |
rs533287490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175524 | TGAGCCATTATCGCC[C/T]ATTGCATTCCCATCC | 25831 |
rs533326794 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192240 | AATCCGCTGAGGTAG[A/G]AGGACAATCGCTTGA | 25831 |
rs533350361 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171205 | TCACTTGAGGCTAGG[A/G]GTTTGAGACCAGCCT | 25831 |
rs533366374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170830 | TCTAATTCTCACAAT[A/C]ATCTTGCTAAGAATA | 25831 |
rs533406047 | snp | G/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136559 | TACTGTTCCAGAGAT[G/T]CAACTGTAGCCAAAG | 25831 |
rs533444686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198061 | CCTAACCTGTACTAG[A/G]TAACTGTATTCTTCA | 25831 |
rs533465110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141477 | ATGCCTATAATCCCA[A/C]CACGTTGGGCAGCGA | 25831 |
rs533493845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177818 | CCATGGAACCTCCTT[C/T]GGTGCCACAAGTGTT | 25831 |
rs533503394 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191467 | TGGGAGGTCAAGGCT[A/G]CAGTGAGCCAAGATG | 25831 |
rs533592304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103473 | CGTGAATCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 25831 |
rs533623850 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175327 | CAGCACTTTGGGAGG[A/C]CAAGGTTGGCAGTTC | 25831 |
rs533654478 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136987 | CCACCACGCCCGGCT[A/G]ATTTTTTGTATTTTT | 25831 |
rs533659150 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190840 | GATTTTTTTAAGAGA[G/T]AAGTTCTCTCTCTGT | 25831 |
rs533688739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149895 | GTGACAGAGTGAGAC[G/T]CCGTCTCAAAAAAAT | 25831 |
rs533691667 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202939 | ACTAAAAATACAAAA[A/C]TTAGCCAGGTATGGT | 25831 |
rs533704315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168696 | TGGATACTCCACTTC[A/G]TTCCAAAAATTATTT | 25831 |
rs533841260 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203754 | ACATGGCAACACTTT[G/T]TTTTTTTATTATACT | 25831 |
rs533941522 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206324 | AAGGCAAAGAACACC[C/T]AACTAAAGGTTCTGT | 25831 |
rs533950262 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112969 | AATTAGGAAATAAAT[A/G]CAAAGGACCATATAG | 25831 |
rs533988166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162483 | ATAACTGGCTCTATT[A/G]GGGGGACTATTTTAT | 25831 |
rs534000640 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155568 | CAAAGAAACATGACA[A/C]AAAGTTAGGCTCTTT | 25831 |
rs534006362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120657 | TTACTATGAGGCAGA[C/G]AGCATGTAAGTACAC | 25831 |
rs534011990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113750 | TTTGTGCATTAACAG[G/T]GTTAATTCAACCTCA | 25831 |
rs534014693 | in-del | -/T | 3.69898e-05 | 0.00430041 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141989 | AAGTCCAAAAAAAAA[-/T]AATTTAAGGATCTTA | 25831 |
rs534048342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106337 | TTGCAAAGTGAATCA[C/T]ATATTAGCAGATGAA | 25831 |
rs534069894 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156402 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 25831 |
rs534152238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199108 | TGTTGAATTTTGACA[C/T]GTTATCAAAGAAGCA | 25831 |
rs534191177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125874 | TTAAAGAAAAACAGG[C/T]AGTATGATCAAGGAT | 25831 |
rs534196410 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157207 | TTCCACTAGTATTGT[A/G]GGCAAATTGTGACCA | 25831 |
rs534306083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206178 | GATATCATACCAAAT[A/G]AAAACCAGTTTTGCA | 25831 |
rs534332947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153395 | AAAAATAGAGACTGG[G/T]TCTCACCTCACCATG | 25831 |
rs534336479 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164256 | CATGGACACTCTTAA[C/G]TGTCTGAATCAGTGT | 25831 |
rs534349651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169857 | CCATTGCACTCCAGC[C/T]TGGTCTACAAGAGTG | 25831 |
rs534367325 | snp | C/G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158551 | AGGCGTGAGCCACCA[C/G/T]GCCCGGCCAAATTAA | 25831 |
rs534380831 | snp | A/G | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099906 | AGTTCTAGCTGAGGC[A/G]TACTTTAAAACTGAA | 25831 |
rs534399436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123482 | TCATGTTATCCATAT[C/T]ATCTAGCACATAAGG | 25831 |
rs534441832 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124811 | CATCTAACAATAAAT[-/T]TTTTTTTTTTTTTTG | 25831 |
rs534445631 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133105 | CTTATTTTCTTTACC[G/T]TTTTTCCATTTGTAA | 25831 |
rs534452919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167070 | CCTAGCTACTTGAGA[A/G]GCTGAGGTGGGGGAT | 25831 |
rs534480074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176701 | AGCACTTTGGGAAGC[C/T]GAGGCAGGTAGATCA | 25831 |
rs534482069 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147980 | GGAGGATTACTTGCA[-/C]TCAGGTATTTTAGAC | 25831 |
rs534489297 | snp | A/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185203 | AAAAATTAGCTGGGT[A/G]TGGTGGCAGGCGCCT | 25831 |
rs534503843 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117873 | CTTTTTTATAATTCA[-/T]TTTTTTTCTCTGAGA | 25831 |
rs534510880 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137101 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 25831 |
rs534512747 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126659 | CTAGATCTACTTCAT[A/G]TATAATCAGATAATT | 25831 |
rs534553180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122757 | AAGTGGAGAATCATA[A/G]ATGCTCAGATTAAAA | 25831 |
rs534563224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180657 | ACCATGTTGGCCAGG[A/C]TGGTATTGAACTCCT | 25831 |
rs534596239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188018 | ACCTTGGCCTCCCAA[A/G]GAGATGGTATTACAG | 25831 |
rs534613484 | in-del | -/T | 0.0611083 | 0.163768 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151391 | TATTTTAGTTAGAGC[-/T]TTTTTTTTTTTTTTT | 25831 |
rs534634857 | in-del | -/AT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153844 | AAAGAAATGATACAA[-/AT]ATATATATATATGTG | 25831 |
rs534661432 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208211 | AAGGAAGGCGTCTCC[C/G]CCCGCTCCTGGGAGG | 25831 |
rs534662672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175634 | GTTGGGAGGCCGAGG[C/T]GGGTGGATCACTTGA | 25831 |
rs534727346 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208842 | ATCCCTCGAGCCCAA[G/T]AAATTGAGGCTGCAG | 25831 |
rs534739659 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147313 | GTGAGAATCCATCTC[-/A]AAAAAAAATAAAAAT | 25831 |
rs534767445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173057 | CGAAGGGGTGCCACT[C/T]TGTTATCTGGATTTC | 25831 |
rs534780682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182590 | GGCGCAATGGCTCAC[A/G]CCTGTAATCCCAGCA | 25831 |
rs534792681 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166028 | TTTTTTTATTTTTCA[C/T]AGAGACAGGGTTTCG | 25831 |
rs534832156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174030 | AAATGGGGATATTAA[C/T]GGTACCTATATCTCA | 25831 |
rs534838198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166364 | GGATGTACTTGGAGG[A/G]TTCCACAACAGAAAG | 25831 |
rs534839907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174852 | CATAATTATAAACAG[A/G]GGAACACTAAAAAAA | 25831 |
rs534875111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189272 | ATCTTGTTGGTTCTA[C/T]CTCCTAACTCGGTTT | 25831 |
rs534878107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158324 | GTAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 25831 |
rs534878398 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31150988 | GTAGTCCTAGCTACT[A/G]GAGAAGTTGAAGCAC | 25831 |
rs534879978 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192981 | ACTCCACCTCAAAAA[A/G]AAATAAAGTAAGACA | 25831 |
rs534902490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180309 | TATGGCGGCTCACAC[C/T]TGCAGTCTCAGCACT | 25831 |
rs534939817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146335 | TTGCTTCAGGTCTCA[C/T]ACTATAAACAAGTGC | 25831 |
rs535003148 | in-del | -/CTTT | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116621 | GCGTCGACATTTTTG[-/CTTT]CTGTTTCTTTTTTTT | 25831 |
rs535014035 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189933 | TTATGATTATAGTGA[A/C]AGTGACCACTGTGTG | 25831 |
rs535058067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125200 | TTTTTTTGAGACAGA[A/G]TCTTGCCCTGTTGCC | 25831 |
rs535060874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103962 | ACAAGAGCAAAAACT[C/T]CGTCTCAAAAAAACA | 25831 |
rs535064824 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126534 | TTTACAAAGCTTATG[-/A]AATCTATTACACTTC | 25831 |
rs535068268 | snp | G/T | 0.000372301 | 0.0136386 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123638 | AACTGAAAAAAAGAG[G/T]ACTAAAGGGATTATA | 25831 |
rs535105104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154132 | TAGACTCTCCTTGTT[G/T]TTTTTTTTTTTGAGA | 25831 |
rs535124081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132607 | TCTGCTAATAAGTCA[G/T]CCTTATAGTTTGAAG | 25831 |
rs535156999 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111492 | CTCCTAACCTCATGA[C/T]CTGCCCGCCTCGGCC | 25831 |
rs535159285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117530 | AATTAGTTTCATAAT[G/T]TATTTGGAGAATGCT | 25831 |
rs535164577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183001 | GCCACTGATTTACGG[C/T]AAATACAGCCAAATT | 25831 |
rs535174724 | in-del | -/AAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200509 | AAAAAAAAAAAAAAA[-/AAA]GGTCACACCTGTAAT | 25831 |
rs535191304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111841 | TGCCATTAGCCACGC[A/G]TGGTGGCGTGCACCT | 25831 |
rs535197103 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209584 | TTTTGAAAGAAGATA[C/T]ATCAGAATTTAAATG | 25831 |
rs535201470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202981 | GTTGTCCCAGCTACT[C/T]GGGAGGCTGAAGCAG | 25831 |
rs535214148 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138928 | AAAGTGATAAAGTTC[C/T]GGGCTAGGACATTAG | 25831 |
rs535308942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117015 | AATACATGTGTATGA[C/T]AGAGAGCTCTCTCAT | 25831 |
rs535329835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202796 | AAGAAGGCCCACTGG[A/G]AAAAAGACTACTGGC | 25831 |
rs535350874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131306 | CAAAAAACACTCAAA[A/T]TATTCAGATGTACAT | 25831 |
rs535377157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103915 | GAGGTTGCAGTGAGC[C/T]GAGTTCGTGCCATCA | 25831 |
rs535404766 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196047 | GAGACGGAGTCTCAC[C/T]CTGTCTCCCAGGCTG | 25831 |
rs535434571 | snp | A/C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190379 | ACAAGTATTGTGGTG[A/C/T]GGCTGGAAATCAGAG | 25831 |
rs535445608 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169005 | GCCGAGATAGCGCCA[C/T]TGCACTCCAGCCTGG | 25831 |
rs535459492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162885 | CCAGTCTGGGCAACA[C/T]AGTAAGACCTTGTTT | 25831 |
rs535504693 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204617 | TGAGAGTCAGGATGA[C/G]GAAAAAAATAAAAAA | 25831 |
rs535512516 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129522 | AGTAGCTCCACAATA[C/T]GGGATCAGCTTTTCA | 25831 |
rs535524975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202024 | GGGCGCGGTGGCTCA[C/G]GCCTGTAATTCCGGC | 25831 |
rs535553660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103474 | GTGAATCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 25831 |
rs535630537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183138 | GTAAAACTCAGTAAC[C/T]CTCTAGCAATCAGTA | 25831 |
rs535639481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160080 | CTATCTCTCTCTCGT[A/G]TACTGAGCCATCATG | 25831 |
rs535642514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140422 | AGAACTTTCAAAAAT[C/T]GTCTTGCAGAGCTGG | 25831 |
rs535666847 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208971 | CTTTAGAAAAAGAAC[A/C]AGTATTTTGGAAATG | 25831 |
rs535693642 | snp | A/C | 0.000183773 | 0.00958398 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144045 | CTAAAAACCACTCTA[A/C]CGAAGGAGTAACTAC | 25831 |
rs535740021 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193255 | TAAAAATATATATAG[A/T]GTGAGATAGTATCAA | 25831 |
rs535757488 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163582 | TACTCCAGCCTGTGC[A/G]ACAGTGAGACCCTGT | 25831 |
rs535775880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174090 | TAAAGAATCTAGATG[C/G]ATAATAAAAGCTCAA | 25831 |
rs535805630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172206 | ACTGAACCATTTTAA[G/T]ATCGTCATTAGTCAT | 25831 |
rs535833054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165173 | TACTGGTATTTGAGG[C/T]ACTTGAATCTTATAA | 25831 |
rs535871103 | in-del | -/CTG | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187246 | TGTAGTCCCAGCTCC[-/CTG]CTGGGAGGCTGAGGC | 25831 |
rs535892710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119155 | TTACACTGTGTCCAC[C/T]TGGATGATCCAGGAT | 25831 |
rs535906896 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126256 | TGTACATCAAAGCTG[G/T]TTGTCTGGTAGGTGG | 25831 |
rs535919655 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105140 | CCCAGTAGCTGGGAT[C/T]ACAGGTATGCGCCAC | 25831 |
rs535948620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125698 | TATAATGACTCTCTT[A/G]AAACTATGGAACATC | 25831 |
rs535958070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118454 | CTTACTTCATTTAAG[A/C]TTTTTAACTACCTTG | 25831 |
rs535969071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171250 | AACCCTGTCTCTACT[A/G]TAAGTACAAAAACTA | 25831 |
rs536008288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180035 | ACAAAATAATTAGCC[G/T]GGTATAGTGGCAAGC | 25831 |
rs536032640 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180341 | TGGGAGGCTGAGGCA[A/G]TTCAAGATCAGCTTG | 25831 |
rs536095498 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151079 | GCCTGGGTAACAGAT[C/T]GGGACTCTGTCTCTA | 25831 |
rs536095510 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142773 | GTGCATCAGCACATA[A/C]AATGATTAAGATCAA | 25831 |
rs536131514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189426 | ATATATTTTTAAAAC[A/C]CAAATCTGTTAATTT | 25831 |
rs536155068 | in-del | -/ACTC | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180370 | TGGCAACATGGCAAG[-/ACTC]ACTATTAAAAAAATA | 25831 |
rs536156942 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132255 | CCAGCCTGACCAACA[C/T]GGAGAAACCCCGTCT | 25831 |
rs536172707 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177354 | TCTACTAAAAATACA[A/C]AACAAATTAGCCGGG | 25831 |
rs536181839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101478 | TGGTTAAGTATGAAA[C/T]GGGCTAATATAAGCT | 25831 |
rs536194775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186048 | GACTCCCCTGGTTTT[C/T]CACTCTAGCTTCCTT | 25831 |
rs536207002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188564 | TCTCAGCCTAAATGT[C/T]ACCTCCTAGACTTTT | 25831 |
rs536265636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182019 | CTGCCTCAGCCTCCT[C/G]AGTAGTTGGGACTAC | 25831 |
rs536295089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115038 | ACTGAAAAGTTGTTA[C/T]ATAGCACATGGCTAT | 25831 |
rs536328106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194371 | AAAAGCTAACTTCCC[C/T]GTATGTAATTTAAAC | 25831 |
rs536359752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110382 | GAAGCTGAAGGTTCT[A/G]CTCTCATGTGTGCTA | 25831 |
rs536360370 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148128 | ATGAGATTATCTTAC[-/T]TTTTTTTTAAAAATG | 25831 |
rs536373618 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186284 | AAAACTCCTGATGTG[A/T]GCCTCTATTCCCAAA | 25831 |
rs536413676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200989 | TGTATTTGTTTTGGT[C/T]ATCACCATATCTTTC | 25831 |
rs536415656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193724 | AGGTCAGGAGTTCGA[C/G]ACCAGCCTGGCCAAC | 25831 |
rs536446505 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159371 | TTGGGACAGAGACTC[A/G]CTCTGTCACCCAGGC | 25831 |
rs536461740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179213 | CACTTGAGGTCAGGA[A/G]TTCAAGAACAGACTG | 25831 |
rs536530997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200082 | ATGGTCCTCTTTCCA[A/G]TGTTCTCTCTCAGTG | 25831 |
rs536600543 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181155 | CATTTTTCTTACCCA[A/G]GGTAAAAACTGTACA | 25831 |
rs536602982 | snp | C/T | 1.65658e-05 | 0.00287795 | missense | HECTD1 | GRCh38.p7 | 14:31116317 | AGCAATTTTTGTACA[C/T]AGTAAAAGATGGTTG | 25831 |
rs536637435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138131 | CTCAAATGCTCACTG[A/G]AGCATTTCAGATTTT | 25831 |
rs536640624 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166138 | GGCGTGAGCCACCGC[A/C]CCCAGCCAAGATAGC | 25831 |
rs536642460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158950 | CTCTGTCTTAAACAA[A/C]AACAAACAAACAAAA | 25831 |
rs536653603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159526 | TGTAGTTTTAGTAGA[A/G]ACGGAGTTTCATCAT | 25831 |
rs536657964 | snp | A/G | 2.21188e-05 | 0.00332549 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173146 | TATATTTAAAAAAAT[A/G]TTTTCTGACCTCCTG | 25831 |
rs536773350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151624 | GTCTCTATCTTCTGA[C/T]CTCACGATCTGCCCT | 25831 |
rs536805922 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102450 | TTTTTTTTTTTTGAG[A/T]CAGAGTTTCACTCTT | 25831 |
rs536830943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152195 | CAACTGGAAAGTTAT[A/G]AGAGATCATACAAGT | 25831 |
rs536831361 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199366 | TTTTCACAAAAAAAT[G/T]TTAACATGTAAGGGG | 25831 |
rs536833244 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110864 | TCGAACTCCTGGCCT[C/T]GAGTGATGTGTCTGC | 25831 |
rs536851873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144732 | CCCTACTCAATACCC[A/G]TGACATAAAGGATAG | 25831 |
rs536918938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144493 | CAGCTATTCAACCAC[A/G]CCCCTGTAGCACCAA | 25831 |
rs536942055 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207596 | GTTCTCGCGTGCGGC[A/C]GCAGCCAGCGGACGT | 25831 |
rs536966633 | snp | A/G | 3.75559e-05 | 0.00433319 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31109585 | CACGTCGGTTCTGTA[A/G]CCATACTATTGCTCT | 25831 |
rs536987670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179298 | GTGGCACATGCCTGT[A/G]GTCCCAGCTACTTGG | 25831 |
rs537003122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182459 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 25831 |
rs537079902 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208172 | CCACGATCTTCCCTC[C/T]TCGCGCACGGAAGTG | 25831 |
rs537111540 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189702 | ACTCGAGCCCAGGAG[A/G]TAGAGGCTGCAGTGA | 25831 |
rs537133067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188732 | AGTTTCCTGCACAGA[A/C]GTGACACTAGCCTTT | 25831 |
rs537168415 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158073 | CATCAAATTTAAAAT[C/G]CACGTTCACTGCAAC | 25831 |
rs537168873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115624 | AATTAGCTAGGCCTC[A/G]TGGTGCACACCTGTA | 25831 |
rs537188347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189136 | CCAAAACTAAAAGAC[A/G]CTTCTCTACCAAAAG | 25831 |
rs537203698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180109 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 25831 |
rs537320223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193559 | CATAAGTCCTTTGCA[G/T]TTCCATATAAATTTT | 25831 |
rs537371748 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146963 | CCTAGAAGAAATCTA[A/G]CCCAGTATTTCTCCC | 25831 |
rs537398766 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177366 | ACAAAACAAATTAGC[C/T]GGGCGTGGTGGTGGG | 25831 |
rs537399736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185846 | AAATGAACGACCCCC[C/G]ACATTCCCTAGGTCT | 25831 |
rs537411410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174176 | AAAATAACATCTGAA[C/T]AATAAAAAGTCATTA | 25831 |
rs537502502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123770 | AAGACAATTTATAAT[C/T]GCTCAGAAACTTACA | 25831 |
rs537549772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131479 | TTTACCTTTGTATAG[A/G]CAATTGCTTAAGTTA | 25831 |
rs537611378 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103424 | GCGGCTGCCTGTAGT[C/G/T]CCAGCTACTCGGGAG | 25831 |
rs537642508 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199679 | AAGATTGTGCCACTG[C/T]ACTCCAGCCTGGGTG | 25831 |
rs537674185 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138203 | AAAACACTTCTGGTT[C/T]CAAGCATTTTGGATA | 25831 |
rs537738510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204286 | GATTGCTGGGTCAAA[C/T]GGTATTTCTAGTTCT | 25831 |
rs537749225 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197641 | TCTATACAAAAGCCA[A/C]TTCTCTCCCAGTTTT | 25831 |
rs537769002 | snp | C/T | 1.66001e-05 | 0.00288094 | missense | HECTD1 | GRCh38.p7 | 14:31105639 | GTAAAACCATATATT[C/T]TTGAGGAAGGGCAAA | 25831 |
rs537774626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111356 | TTCCCAGGTTCACGC[C/T]ATTCTCCTGCCTCAG | 25831 |
rs537888401 | snp | C/T | 0.000430792 | 0.01467 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135657 | GTCACCTTAATAATG[C/T]TGTTTTCAAGCACGT | 25831 |
rs537912135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150350 | TAATACTCAATTGCC[C/T]GTAGCTTAATCTTTT | 25831 |
rs537928085 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114838 | ACAAAATGGTATAGC[C/G]TACTATCTACGTAGG | 25831 |
rs537937940 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099667 | TCCTTTCACCTATAA[A/G]CACAGATATGGTAAT | 25831 |
rs537942672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107395 | TATAATTTTATTAAA[C/T]AGCTTTTGGTGACTA | 25831 |
rs537960037 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133822 | CATTACAAGAATCAA[C/G]AAATCAAAGGAAAAA | 25831 |
rs538019222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101969 | TACCAAAGGGGATCT[A/G]AAATAATTTTTATTC | 25831 |
rs538021551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156178 | CGTGAACCCAGGAGG[C/T]GGAGCTGGCAGTGAG | 25831 |
rs538083077 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180966 | TAGATGGAAGAAATG[-/AA]AAGAGACTGTTAAAG | 25831 |
rs538092689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206323 | AAAGGCAAAGAACAC[A/C]TAACTAAAGGTTCTG | 25831 |
rs538118806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113037 | GAGGTAGAAAAGAAA[A/G]TAAAGGGAATATTAG | 25831 |
rs538144890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204902 | AGTAATATAAACTTT[A/C]TTCCCACCTAAAACA | 25831 |
rs538151665 | in-del | -/A | 0.450357 | 0.149522 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131028 | CCCAAAAGATAAACC[-/A]AAAAAAAAAAAAAAA | 25831 |
rs538194586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101564 | TTGGGAGGCTGAGGC[A/G]GGTGGATCATCTGAG | 25831 |
rs538219376 | in-del | -/T | 0.00874735 | 0.0655527 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099663 | CTTTCCTTTCACCTA[-/T]TAAGCACAGATATGG | 25831 |
rs538235231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151341 | CCACCCTTAGCCAAG[C/T]GAATCAAATATACTC | 25831 |
rs538272752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143533 | TTTCACATAAACTTC[C/G]TAAACTTTTTTCCTT | 25831 |
rs538284145 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148223 | ACCTGATGGAAGCAT[-/A]AAAAAAATTAGTCAA | 25831 |
rs538304636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120908 | TGCTGGCAAGGCACA[A/G]TGGCTCATGCCAAGG | 25831 |
rs538316775 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138274 | AAAAGATGCAAAATA[A/G]TTTTTAATCCAATAC | 25831 |
rs538325604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206860 | CCACGTAACGCAGCC[A/G]CAAGTGTGGGAAGCC | 25831 |
rs538333076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185992 | CTACATTTCTTTCAC[A/G]GTCTGGAATGAGTAT | 25831 |
rs538338095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200130 | TTGTAACCTGAGTCA[A/T]CCACGACACTTCCTT | 25831 |
rs538364083 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136845 | CTTTTTTTCTGAGAC[A/G]GAGTCTCACTCTGTT | 25831 |
rs538378060 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101780 | CTGGACAATAAGAGC[A/G]AAACTCCATCTCAAA | 25831 |
rs538395954 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186482 | CACCTGAGGTCAGGA[A/G]TACGTGACCAGCCTG | 25831 |
rs538432564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164347 | CCACCTTGTTTTTTC[A/G]AGACAGGGTCACATT | 25831 |
rs538441061 | snp | A/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150106 | TTAGATAATTCCAAG[A/G]CTGCTGCATCACTCC | 25831 |
rs538441397 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31173916 | AGCAAAGTGATTAAG[-/C]ATGTGATCTGCCTAT | 25831 |
rs538444738 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157403 | CAATGTTACATTTTA[C/T]ACACTCTGCTAAAAA | 25831 |
rs538450463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141797 | TAGACTTATTTTAGA[A/G]GAAGTATACCAACTG | 25831 |
rs538495317 | snp | C/T | 1.69183e-05 | 0.00290841 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101342 | AAAAGAACAAAAATA[C/T]AGTTATATTGAGTTG | 25831 |
rs538513861 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149635 | TTTGTTTCTACAGTG[A/G]CTCACACCTGTAACT | 25831 |
rs538554688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198344 | ATTCAGACTTGGCTA[C/T]CTGGCAAACATTTTT | 25831 |
rs538555046 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104034 | GTATCAGAGGCTGGG[A/T]ATGTTGCATGTGGGG | 25831 |
rs538615035 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104471 | AACAGAGAGAGAACA[C/T]TCAGTTGCTATGGTC | 25831 |
rs538652924 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147274 | AGCCGAGATCGCACC[A/G]CTGCACTCCAGTCTG | 25831 |
rs538683316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128340 | TCATCTATTTCCTCA[C/T]GCAACTTTGCTTAAT | 25831 |
rs538687077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145254 | CAGAAAAAAACGTAT[C/T]TCTCTAAACTACTTA | 25831 |
rs538692104 | in-del | -/ATTC | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151302 | TTATAAGTAAATAAA[-/ATTC]ATTCATTCATTCATT | 25831 |
rs538743743 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200516 | AAAAAAAAAAAGGTC[A/C]CACCTGTAATCCCAG | 25831 |
rs538749012 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141589 | GAGCAAAATCTTGTC[C/T]GAATTTACAAAATAA | 25831 |
rs538753947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109336 | TGCAGTGAAGATACA[C/T]ATTGGGCTGGTTCCC | 25831 |
rs538782956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102325 | AAAGTTTAATATAAA[C/T]GTAGTATATAGCCCA | 25831 |
rs538800532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192203 | ATACAAAAATTAGCC[A/G]GGTGTGGTCTTGAGC | 25831 |
rs538808869 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100504 | TCTCTATGTTTTAAG[A/G]AAGCAGGATTTTTGA | 25831 |
rs538842839 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147265 | GTTGCAGTCAGCCGA[A/G]ATCGCACCGCTGCAC | 25831 |
rs538852808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165593 | TCCTCTCTACTTTCT[C/T]AACATTATTCTCGGA | 25831 |
rs538859663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142690 | AAGTGTTCTGCCCAC[C/T]TCAGCCTCCTAGAGT | 25831 |
rs538880028 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207535 | GAAAAGCCGCGCCTC[C/G]TCCCTCCCCTTCCTC | 25831 |
rs538934397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198973 | TCTAGGAGGTGGAGG[C/T]TGCAGTGAGCCAAGA | 25831 |
rs538966717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206917 | CGGCGGCGACCAGCG[A/G]GGTTGACCCCACACC | 25831 |
rs539016067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144616 | TGTCCTTCTGGTTTG[C/T]TTTCAATCATTTAAA | 25831 |
rs539031466 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184698 | GTGAGCCATGATCAC[A/G]CACAATGCACTTTAG | 25831 |
rs539091043 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152066 | GAATATGTGGAGGCT[C/G]AGTTCACTATTACGG | 25831 |
rs539096251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140465 | ATGCTGGAGTCCCAG[A/C]TACAAGGGAAGCTGA | 25831 |
rs539100509 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160767 | CCTCGACCGCCCAGG[C/T]TCAAACAATCCTCCC | 25831 |
rs539142315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104001 | AAAGTTGATCTCATA[A/T]AGGTAAAGAAAAGAA | 25831 |
rs539144105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112334 | ATTCCCTCTATCAGT[A/C]TTGACAGTATAGTTG | 25831 |
rs539157239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203620 | AAAAATTACATCATA[C/T]TATATATGAATAAAG | 25831 |
rs539164227 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181178 | ACTGTACATCAAAAA[A/T]AAAATAAAATTTAAG | 25831 |
rs539164659 | in-del | -/ACTTTGG | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125625 | CAATGAATTTATAAC[-/ACTTTGG]TGTAATCATCATCAT | 25831 |
rs539169271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196748 | GACAGAGCAAGACTC[C/T]GTCTCAAAACAAAAA | 25831 |
rs539181471 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104777 | TCCCAGGCTCAAACT[A/G]TTCTCCCACTTCAGC | 25831 |
rs539206013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111912 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 25831 |
rs539268622 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141224 | TGAGCCACCGTGCCT[C/G]GCCTACTTCTTCTTA | 25831 |
rs539325099 | snp | C/T | 8.28988e-05 | 0.00643759 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121475 | CAGAGCGGGAGCCAG[C/T]TCGACGTTGCAGGGA | 25831 |
rs539335803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124383 | AAACACAACATGGTA[C/T]AGTATTCGTGCCTGC | 25831 |
rs539351134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165139 | AGCAGACTGCTTGTA[C/T]TTTAATGTCAGCTCA | 25831 |
rs539354585 | in-del | -/AAAAACAAAAAC | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111983 | GAGACTCTGTCTCAA[-/AAAAACAAAAAC]AAAAACAAAAACAAA | 25831 |
rs539372104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117655 | AACAGAGGCATATCC[C/T]AGTTACTGGACATAA | 25831 |
rs539394163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197364 | CATCAAACCCAAAAC[A/G]TGTGCATCTAACGTC | 25831 |
rs539398363 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138620 | ACAAAACACAAAGTA[A/G]CCCTCCACATCTTTT | 25831 |
rs539453252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148541 | GGTATTTAGTATAGG[C/T]ATAAAAATTATATGT | 25831 |
rs539454466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156301 | TGGAATGCGGTGGTG[C/T]GATCTCGGCTCACTG | 25831 |
rs539518170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196107 | CAACCTACACCTCCC[A/G]AGTTCAAGCGATTCT | 25831 |
rs539572837 | snp | G/T | 3.38862e-05 | 0.00411606 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113237 | ATAAACTGACTTGCT[G/T]TAAAACTGCTATAGA | 25831 |
rs539576169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118204 | TAGAGACGGGATTTC[A/G]CCATGTCGGTCAGGC | 25831 |
rs539577265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163021 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 25831 |
rs539613139 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168381 | GGGTGCCATTTCCGG[A/G]TCTCCTTTGGGCTCA | 25831 |
rs539654507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202986 | CCCAGCTACTCGGGA[A/G]GCTGAAGCAGGAGAA | 25831 |
rs539664002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154243 | TCAAGCAATTCTCCT[A/G]TCTCACCCTCCCAAG | 25831 |
rs539665746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169176 | AGTCACAATCTCAAA[C/G]AACATAGAAAATTAA | 25831 |
rs539714103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132932 | CAAGATAAAGAAAAA[C/T]ATAAGAAATTAAAAT | 25831 |
rs539750826 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134056 | TTAAAAAAAAAAAAA[A/G]GATGGTTTACAAAGA | 25831 |
rs539768702 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129951 | ATAGATGTGAGCCAC[C/T]GCACCTGGCTTGGTT | 25831 |
rs539781522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113692 | CCATGGTCAAAGTCT[A/G]CATTCAGATCCAATG | 25831 |
rs539800890 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31140591 | AAGACTCCATCTCTT[-/A]AAAAAAAAAGAAATC | 25831 |
rs539835627 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125005 | GTAGAGACAGGTTTC[A/G]CCATATTGGCCAGGC | 25831 |
rs539872643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125328 | TGCAGGAGTGGGCCA[C/T]CACACCTGGCTAATT | 25831 |
rs539875159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205048 | CTGGAGTTCAAAACT[A/G]TAAATACAAATGTAA | 25831 |
rs539927685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182803 | TTGCAGTGAGCCAAG[A/G]TCAAGACACTGCACT | 25831 |
rs539936628 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181901 | AAGAATGTCTTTTTC[-/T]TTTTTTTTTTTTTTG | 25831 |
rs539937965 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182775 | AGAATGGCATGAACC[C/T]GGGAGGCAGAGCTTG | 25831 |
rs539946222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119906 | AAACATAATAAGATG[A/C]AAAATTTCATTGTTG | 25831 |
rs539956032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169749 | GCCGGGTGTGGTGGC[A/G]CATGCCTGTAATCCC | 25831 |
rs539979598 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126928 | CTCCCACCTTGGCGT[C/T]CCAAAGTGCTGGGAT | 25831 |
rs540018836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189653 | TATAGTCCCAGCTAC[C/T]GGATGGGGGTTAGAG | 25831 |
rs540129325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203025 | ACCTGGGAGGCGGAG[G/T]TTGCAGTGAACCAAG | 25831 |
rs540133219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103766 | TGAGGGTGGGAGTTC[A/G]AGACCAGCCTGACCA | 25831 |
rs540182829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184360 | TTGGGAGGCCGAGCC[A/T]GGTGGATCTCTTGAG | 25831 |
rs540212243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132989 | ACTAGGGGAAAAAAC[C/T]GGAAGTGTGTCTTGA | 25831 |
rs540212494 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130478 | ATTAACTTCCAAAAG[C/T]AAAAAAAAAATTGTC | 25831 |
rs540248005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168756 | GAAAACTTAAAACTT[C/T]GGTCAGCCGGGAGCA | 25831 |
rs540274931 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140547 | GGCACCCGTAAATAG[A/C]CACTGGACTCCAGCC | 25831 |
rs540284313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134387 | AACATTTTAAGTCAG[C/T]CTTAATTCTATAACG | 25831 |
rs540299247 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162191 | TGAGCCAAGATCATG[C/T]TACTGCACTCCAACC | 25831 |
rs540364837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183284 | TACATGAGTAACAAA[C/T]TTTTGAAAGTTAACT | 25831 |
rs540365906 | snp | C/T | 4.97715e-05 | 0.00498831 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148844 | CTTACTTTGTTACAA[C/T]TTAACATATTCATTT | 25831 |
rs540369802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175381 | TAACCTGGGCAACAC[A/G]GCAAAACCTGATGTC | 25831 |
rs540375032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191265 | GTGCAGTGGCTCACG[C/T]CTGTAATCCTAGCAC | 25831 |
rs540383158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148585 | AGAAAACACAGAAAA[C/T]AGAAAAACTAAAAAT | 25831 |
rs540406115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147582 | GCCAACATGGTGAAA[C/T]CCCGTCTCTACTAAA | 25831 |
rs540432756 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194340 | GTTACATGACTCATA[A/G]CAATGTACAATAATA | 25831 |
rs540493290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118758 | AATGAGCTGGGCATG[A/G]TGGTGCATGCCTGTA | 25831 |
rs540495919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111962 | CTCCTGCCTGGGCGA[A/C]AGAGCGAGACTCTGT | 25831 |
rs540510955 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105093 | CCGCAACCTCACCTC[C/T]CGGGTTCAAGCAATT | 25831 |
rs540526080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119361 | TAGAGGGCATGACTG[A/T]AACCACTGGATAGCC | 25831 |
rs540534677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104180 | AGAAGCTAGAAGAGA[A/G]TAATTTGAATGTTCC | 25831 |
rs540570718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146806 | TGCAGGGAGCTGAGA[C/T]TGTGCCACTGCCCTC | 25831 |
rs540596075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162004 | GGAGGCTGAGAAGGG[C/T]GGATCACATGAGGCC | 25831 |
rs540603492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152902 | GAGGCAGGAGAATTG[C/T]TTGAACCCGGGAGGC | 25831 |
rs540628976 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185326 | CCTGGGCGACAGACA[A/C]AGAGAGACTCAGTCT | 25831 |
rs540674880 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120859 | TTGTTTTGTTGGAAA[C/G]AATTAGTTAATATAC | 25831 |
rs540699509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105832 | CCTCTCCTCCTCCAA[C/T]AAAATCAGTACACCA | 25831 |
rs540703776 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194582 | GTGAGTACTATATTA[C/T]TAATATAATACCAAT | 25831 |
rs540722267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197869 | GACCTTGAGAATGTT[A/G]CTAAATCTAAAGGAC | 25831 |
rs540734412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198399 | TCATTTCAAGGAAAA[C/T]GATCAACTGTATTTG | 25831 |
rs540745662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109926 | AAATGTTTCCTATCA[C/G]AGAAATTTAGAAATG | 25831 |
rs540759489 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201938 | AGCACTGACACATCA[C/T]AGAAGAAGTTATATT | 25831 |
rs540766945 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152393 | CAGAGTTTTGCCATG[A/T]TACCTAGGCTAGGCT | 25831 |
rs540770817 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182827 | CTGCACTCCAGCCTG[C/G]GCAATAGAGTGAGAC | 25831 |
rs540782200 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163143 | GAAAAGAAAACCAGA[C/T]CACACACGGTGGCTC | 25831 |
rs540829393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165890 | TTGCTCTGTTGCCTA[A/G]GCTGGAATGCAGTGG | 25831 |
rs540829550 | in-del | -/AAC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192628 | AAAGGGAATATCACA[-/AAC]AACTCTATGCCCATA | 25831 |
rs540857229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204550 | ATTTTTAAAATACCA[A/G]AAGTAACTTTCAGGT | 25831 |
rs540907494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115679 | GTGGGAAAATCACCT[A/G]AGCCTGTGGAGTTTG | 25831 |
rs540930171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122419 | TCTGTGGCTCAGGTT[A/G]GAGTGCAGTGATGCA | 25831 |
rs540943030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203949 | TTCCCCTTCCTGTGT[A/C]CAAGTGTTCTCATTG | 25831 |
rs540975600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169230 | ATAAGGATATACATA[C/T]ATAATTATTTGACTT | 25831 |
rs540990017 | snp | A/G | 0.000201484 | 0.010035 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103074 | AAACCCATCTACATC[A/G]TACATGTAACGGAAA | 25831 |
rs541035422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137704 | GAGATCACGACACTG[C/T]ACTCCAGCCTGTGCA | 25831 |
rs541107490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111591 | TGAATTCACAGAGAA[C/G]AGGTTCCAGCAGCTC | 25831 |
rs541112054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174346 | GGTCAGGAGTTCAAG[A/C]ACAGCCTGGCCAATA | 25831 |
rs541141083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102630 | AAACGAGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 25831 |
rs541183290 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209141 | TTTAGATGTCATGAG[C/T]GTGAATTGGAGCTGC | 25831 |
rs541243048 | in-del | -/AT | 0.00914312 | 0.0669923 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162532 | ACTCTGCTAGTTATC[-/AT]AAAAATTTCATTGCT | 25831 |
rs541258037 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207703 | CGCGGCGGGGAGGCC[A/C]AGTCCATCGCGAACC | 25831 |
rs541258500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130848 | CTCTATTTTTTTCTG[C/T]ATGCTGAAATAATCT | 25831 |
rs541258613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108724 | AATGAAAGTCTGTAT[A/G]TAAAGTGAAAGATGT | 25831 |
rs541290180 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152697 | TGAGACCCGCATCTC[C/T]ACAAAAATAAAATAA | 25831 |
rs541313638 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191126 | TACAGACCTGAGTCA[C/T]TGCGCCTGGCCTCAT | 25831 |
rs541317781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138304 | CATTTTAGTAAGCAA[A/C]AAGCACAGGACTAGC | 25831 |
rs541354872 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207243 | GAACAAAGGGGCCAG[C/T]GGGGAAGTCGGCAGC | 25831 |
rs541363874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165386 | AGTTCCTATCTCAAT[C/G]AACACTTGTCTGTTT | 25831 |
rs541420965 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156132 | GGCGTCTGCAGTCCC[A/C]GCTACTGGGGAGGCT | 25831 |
rs541424772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146590 | ATCAACAATACATAT[C/T]AGGCTGGGCGCAGTG | 25831 |
rs541438680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153756 | TATATAATGTATATA[C/T]ATAATGCTATATATA | 25831 |
rs541459563 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139054 | CAGATATATATATAT[A/C]TATATCTGTATGGGG | 25831 |
rs541478780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116745 | AAGCAATTCTCCTTC[A/G]TCAGCCTCCCGAGTA | 25831 |
rs541486298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145814 | CAGTAATTTTTAAAA[C/T]TTTTTTCTTACAATT | 25831 |
rs541501161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166769 | GGTGGGAGGATTCCT[C/T]GAGCCCAGGAGTTCA | 25831 |
rs541605327 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170953 | CTTCAGAGTGGACTA[A/G]CCTCGTACTATACCA | 25831 |
rs541649128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159618 | CGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 25831 |
rs541662002 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154193 | TGCAATGGCACGATC[C/T]GATCTCGGCTCACTG | 25831 |
rs541666072 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110920 | ATAGGCATGGGCCAC[C/T]GTGCCCAGCCTGAAA | 25831 |
rs541681024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153110 | AAAATAGAGATGGGT[C/T]GGCCAGGCGTGGTGG | 25831 |
rs541723045 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207177 | AAAGGAGCCGGCCTG[A/G]GGCTCTGGCGCGGGC | 25831 |
rs541724580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116543 | AGGAAACAAGGCTAC[A/G]TGAAATCCAAACCTC | 25831 |
rs541776108 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181513 | CCAGCTACTCGGGAG[A/G]CTGAGGCAGGAAGCT | 25831 |
rs541808173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188925 | CCACCTCACTCTACC[C/T]ACCTGCCCCCAACTT | 25831 |
rs541811072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188850 | ATGCCCAATCCCTCA[C/T]AAATATACCCCCATC | 25831 |
rs541842473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154454 | AGCCAAGTGCTACCA[C/T]GCCTGGCTCATTTTT | 25831 |
rs541845386 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131115 | TAAGAACCCTCTCTG[A/C]CATAGAGACTCAAAG | 25831 |
rs541847184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196423 | TTCATTTCCCTATTA[C/T]TCTGCCATTGGGTAG | 25831 |
rs541882200 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185419 | CATTTTCAGAGAAAC[C/G]CTGTGTTGACAGATA | 25831 |
rs541921877 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209931 | CCCTTAACGTAGAAA[G/T]AGGACTTGGAAGCTA | 25831 |
rs541933861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194816 | AGAAAGAATTTCCCT[A/G]GGAACTGTAATATTT | 25831 |
rs541947220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161002 | ATATTAATTTTTTGC[C/T]GTGTTTCCTCTTGAA | 25831 |
rs541971293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203186 | CCAAGAATCTGAACC[C/G]AAGTCTCTGATGCCA | 25831 |
rs541973614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167349 | TAGTCTCAGCTATTC[A/G]GGAGGCTAAGGTGGG | 25831 |
rs541992778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152436 | CTCAAGCGACCTGTC[C/T]GCCTCGGCCTCCCAA | 25831 |
rs542028126 | snp | G/T | 5.3843e-05 | 0.00518832 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116506 | ATACTAAAACAAGCA[G/T]TCCAAGAAAGGCCAC | 25831 |
rs542034879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160390 | ACTATTTATTTTTGT[G/T]TAAACAGTTTCTTCA | 25831 |
rs542035227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167966 | GCCAAATCTCATTTA[C/T]CTGTATAACTCCTCC | 25831 |
rs542058218 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207826 | CCGGCGGCGACCCCG[C/T]CGGCGGCCACCTGGG | 25831 |
rs542119546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200723 | GAGGTGGAGGTTGCA[G/T]TGAGCTCAGATCACG | 25831 |
rs542133834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159083 | CCTTGAGGTGAATGA[C/T]AGAAGGATAAAGAGG | 25831 |
rs542134279 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151696 | GCCTGACTCAGCATG[-/T]TTTTTTTTTTTAAAA | 25831 |
rs542138852 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170029 | CCCAATTTCTTTAAA[G/T]AGAGGTACTGTTTAA | 25831 |
rs542172959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166491 | GAGCTGAGTTTTTGT[C/T]AAAGCCAATTAGAAG | 25831 |
rs542200702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174406 | AAAAATTAACCAGGC[A/G]TGGTGGTGGGCACCT | 25831 |
rs542230729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155162 | CTGGCCTGGCCAATA[C/T]GATGAAACCCTGTCT | 25831 |
rs542232948 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203809 | AACGTGCAGGTTTGT[G/T]ACATATGTATACATG | 25831 |
rs542325681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111696 | TACCTTTCTCTTTGG[C/G]TTCCTTCTTTTTCTG | 25831 |
rs542348223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112067 | CTTCCAGTTTAGCCA[C/T]GGTAACACTTGTGGG | 25831 |
rs542360247 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136008 | GGCAACAGAGCAAGA[-/CT]CTGTCTCAAAACAAA | 25831 |
rs542409262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178567 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 25831 |
rs542596931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157631 | TCAAGTAAAAAGTAC[C/T]ACAACTACTAAGAAA | 25831 |
rs542602886 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122104 | GAGTAGCTGGGATTA[C/T]AAGCACAAGCCACTG | 25831 |
rs542646513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129752 | CTTTTATTTCCCTTA[C/T]TTCTGAACTATTCAG | 25831 |
rs542648238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107822 | TACCTTTTTTCAAAA[C/T]AGCAGTGTATATATA | 25831 |
rs542669632 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150669 | TTAGAGCACTACACA[A/C]AACAACATAATAACC | 25831 |
rs542712556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121030 | TTAGTGATCATTAAG[C/T]GTTAGCTATTAATAA | 25831 |
rs542721763 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206555 | CGACAATTATATACA[A/C]GATTTATCTATGAAT | 25831 |
rs542791929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180479 | TTTGTTTTTTGATAG[G/T]CTCGTTCTGTTGACC | 25831 |
rs542799665 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101970 | ACCAAAGGGGATCTG[A/C]AATAATTTTTATTCC | 25831 |
rs542872156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120228 | TCTCTACTAAAAATA[A/C]AAAAAATTAGCTGGG | 25831 |
rs542887484 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185317 | GCACTCTAGCCTGGG[A/C]GACAGACAAAGAGAG | 25831 |
rs542914382 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151707 | GCATGTTTTTTTTTT[A/T]AAAAAAAATGTATAA | 25831 |
rs542930820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108550 | TGTAAACAACTGGGC[A/G]TGGTGGCTCAAGCCT | 25831 |
rs542967589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101667 | CGTGGTGGCGCACGC[C/T]TGTAATCCCAGCTAC | 25831 |
rs542994678 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172400 | CAGGAGTTTGAGACC[A/C]GCATGGCCAACATGG | 25831 |
rs543054690 | in-del | -/AACATCTTTATATAA | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147428 | GGAAATAAAGATGTG[-/AACATCTTTATATAA]AACATCCGCTTCAAA | 25831 |
rs543105776 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196838 | GATACTGTATCTGCT[-/A]AAAAAAAAAACAAAA | 25831 |
rs543143805 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158284 | TTTTGGAGACAGAGT[C/G]TCGCTCTGTTGTCTC | 25831 |
rs543232197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165207 | TGCCTGCTCTACAGA[C/T]CTCCTGAACTGAAAA | 25831 |
rs543242808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143761 | AACTTTCATTGTTCA[C/T]ACATTATGCATATAA | 25831 |
rs543243688 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190826 | TTTTTTATACATTGA[-/T]TTTTTTTAAGAGATA | 25831 |
rs543285280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101143 | AGTAAAGTAACTAAA[C/T]TTCATTTGGATTCCC | 25831 |
rs543296854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121776 | TTAAAACTCAACTTA[C/T]CAATTTTTTTGAAAT | 25831 |
rs543304538 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143199 | CGGGCGGGTCACTTG[A/C]GGTCAGGAGTGCGAA | 25831 |
rs543331902 | snp | C/T | 0.00279258 | 0.0372817 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106435 | TAATCTTCTAAAGGT[C/T]TGATGATTAATAAAC | 25831 |
rs543365424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101772 | ATTCCAGCCTGGACA[A/G]TAAGAGCGAAACTCC | 25831 |
rs543388306 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151744 | TGTAGCTCAGCCTGT[G/T]TTCCTAAAACTTTTT | 25831 |
rs543425013 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143896 | AACCTTTAGCAAATT[A/G]TAACTGGGAACTTAG | 25831 |
rs543458479 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208472 | TTTCACACGCATTCA[C/G]AATAAAGGATGCATG | 25831 |
rs543500620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116614 | TCTCTAGGCGTCGAC[A/G]TTTTTGCTTTCTGTT | 25831 |
rs543503209 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207127 | GAGCTGCGCCCGGAA[C/T]TCGAAGGCCTGGCAG | 25831 |
rs543525940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115132 | AGAAATAACAATGAT[A/C]AGGAGTGCTTATGTT | 25831 |
rs543526551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200335 | TACTCATCCTTCCTA[C/G]CTCTAGGAAAAACCA | 25831 |
rs543564118 | snp | G/T | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122942 | TATTCTTGGTCCTCC[G/T]GATTGTCATCTTCAT | 25831 |
rs543564437 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192655 | CCCATAAATTTAAAT[G/T]CAGATTAAACAGACA | 25831 |
rs543598628 | snp | C/T | 1.65636e-05 | 0.00287776 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173385 | TTCATCACCCTGCAA[C/T]GCACTTTCAATTGAA | 25831 |
rs543677245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127511 | CGTGTGCCACCACTC[C/T]CGGATAATTTTCTTT | 25831 |
rs543707549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121054 | TTAATAAACTACTAC[C/T]GCTGCATCTACTACC | 25831 |
rs543717074 | snp | C/T | 0.000160304 | 0.00895132 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144955 | ACCTACCAAAATAAA[C/T]ACAACAAATGTGAAT | 25831 |
rs543741836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170791 | ATATGCTGATTACTA[C/T]AGTAAATCTATACAA | 25831 |
rs543757395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193849 | GAATCGGTTGAACCC[A/G]GGAGGTGGAGGTTGC | 25831 |
rs543793676 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185167 | CTAACACGGTGAAAC[C/G]CCATCTCCACTAAAA | 25831 |
rs543883193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172457 | AAAAATTAGGCGGGT[A/G]TGGTGGCACATGCCT | 25831 |
rs543897803 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115626 | TTAGCTAGGCCTCGT[C/G]GTGCACACCTGTAGT | 25831 |
rs543908091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115984 | TTAGTACTCATACAC[A/G]ATCTTAGACAAAGAA | 25831 |
rs544029772 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112923 | CCTATAAGGCAATTA[C/T]TAAAAATTACCAAGT | 25831 |
rs544042520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183770 | TAAAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 25831 |
rs544089694 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196973 | AAGCAATCTCTTCAA[G/T]TCACTCCTTCAGTAT | 25831 |
rs544089985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189810 | TATTTTCCAATGATG[A/T]CCACAACATTATCTA | 25831 |
rs544104098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190298 | CTGTTAGCATAATTC[A/T]TGTTTAATACTACTA | 25831 |
rs544153145 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194948 | AAAGGGCATTATCTG[C/T]AGTAGAGATATTTTA | 25831 |
rs544184201 | snp | A/G | 3.31653e-05 | 0.00407204 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169465 | CACCATGCCGTAACA[A/G]AGTCTAGAGAAGAAA | 25831 |
rs544194864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140444 | CAGAGCTGGGCAAGG[C/T]GGTATATGCTGGAGT | 25831 |
rs544195129 | snp | C/T | 9.93624e-05 | 0.00704779 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135091 | AAAGCTGAATTATCA[C/T]GACTTAGTATGTCTT | 25831 |
rs544215628 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163063 | GGGTAAGATCCTGAC[A/G]CACACACACACACAC | 25831 |
rs544235490 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136000 | TCCAGCCTGGCAACA[C/G]AGCAAGACTCTGTCT | 25831 |
rs544241120 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119519 | AAATTTGAAATAATT[G/T]GTAATTTGCTCCTTT | 25831 |
rs544252648 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177735 | GGAACTGAAGTGCAC[C/T]GAAGCAGCACATAAC | 25831 |
rs544282466 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131193 | CTACATTTGTCAGAT[G/T]AGCAAAAATAGGCCT | 25831 |
rs544306434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126092 | ATTAAATGATGATCA[C/T]ACAGTGAAATATTTG | 25831 |
rs544311970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126951 | GCTGGGATTATAGGC[A/G]CAAGCCACCACTTCT | 25831 |
rs544414734 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127197 | CCAGGCTGGTTTCGA[A/T]CTCCTGACCTCAAGT | 25831 |
rs544442982 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130151 | TTTCTTACAATTTGG[A/G]CTAACCTCTCAAAAT | 25831 |
rs544476586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104976 | AGCCACCACCACACC[C/T]GCACACCCGACCACC | 25831 |
rs544524430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105956 | ATTGCATGAAACCAC[C/G]TTTCTATATTTTACT | 25831 |
rs544539695 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204589 | ATGAAATCTATGAAC[A/G]CAATTTTTAACTTGA | 25831 |
rs544649101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205451 | AATCAATTTCATGGT[A/G]CAGAAATAGATACCT | 25831 |
rs544686076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177502 | AGACACAGCAACTGT[C/G]TCAAAAACAATAATA | 25831 |
rs544687198 | snp | A/C | 0.000399281 | 0.0141238 | splice-donor-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31100114 | TCACATGACACAGTT[A/C]TGTACGCTGCAAACA | 25831 |
rs544691629 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206590 | AGTTGGTTAGGAATT[C/T]TGGCAGTCTTGGCAA | 25831 |
rs544716227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191957 | GAGGTTGCAGTGAGC[C/T]GAGATCACACCATTG | 25831 |
rs544729856 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175205 | ATCACAGAAACAATG[A/C]GCTCTCCAAATTTAT | 25831 |
rs544743726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119607 | TGCATACACAAAACT[A/G]AAAAAAAATTTTTAA | 25831 |
rs544763776 | snp | C/T | 1.70214e-05 | 0.00291726 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169520 | ACTTTATTTCTTTGA[C/T]ATCCAACTATGTAAA | 25831 |
rs544779185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176852 | TAAGGCAGGAGAACC[A/G]CTTGAACCCAGGAGG | 25831 |
rs544779254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185271 | GTGAACCTAGGAGGC[A/G]AAGCTTGCAGTGAGC | 25831 |
rs544898014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183882 | CCAGTTAATTTTTTT[A/G]TTTTTGGTAGAGACA | 25831 |
rs544914074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205341 | TGAAATTTACAAACC[A/G]ATAATCGGCTTTAAC | 25831 |
rs544946340 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167538 | TAAAGGAGCAAGAGA[C/G]AAAAAGCAGAATGAT | 25831 |
rs544946900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163848 | AACCCAGGAGGCGGA[A/G]GCTGCAGTAAGCCAA | 25831 |
rs544949693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163778 | AGCCGGGCATGGTGG[C/T]GCGTGCCTGTAATCC | 25831 |
rs544958929 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131448 | AATCGAGAAGAAAAA[A/T]AACCCACAGTGTCTA | 25831 |
rs545009674 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131520 | AACATTTGTACTTCA[A/G]TAAAATGCTTATGTA | 25831 |
rs545030319 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128704 | GTGGCATTAGTCCGT[A/G]CTATGTTTGCCACTC | 25831 |
rs545043815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156595 | AGGAAATGGGGCAAA[A/G]TGTTAATAACTAGTG | 25831 |
rs545065723 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137071 | TCGTGATCCACCCTT[C/T]TTGGCCTCTCAAAGT | 25831 |
rs545098742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120149 | CAGCACTTTGGGAGG[C/T]TGAGGCAGGCGAATC | 25831 |
rs545133789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169914 | AGCAGCCTATCGTAA[C/G]TTGAAAAACTTATGA | 25831 |
rs545165898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193012 | TGCTACCAAAACTCA[C/T]GCAAGCAGCATTAGA | 25831 |
rs545244011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141250 | TCTTATATATTTTGA[A/G]AAAATACTAAAGAGC | 25831 |
rs545283306 | snp | G/T | 0.000172747 | 0.00929214 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106604 | CAAAAGCTTTAAAAC[G/T]TATTCATGCATTGGA | 25831 |
rs545320249 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170028 | TCCCAATTTCTTTAA[A/G]GAGAGGTACTGTTTA | 25831 |
rs545334156 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198655 | TTTTTGCAAAAGTAA[A/C]CATGGGTAAAACAGT | 25831 |
rs545391407 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131875 | CTACTATTCAACTCA[A/G]TATAACAATAATAGT | 25831 |
rs545429598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124093 | CAGCATCTTAAATTT[A/G]ATAAAATATGTTACC | 25831 |
rs545513588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186181 | ATCACAAAAACTCCC[C/T]AAGTATTTTCTCCAC | 25831 |
rs545529529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178747 | GAGGTTGCAGTGAGC[C/T]GAGATTACGCCACTG | 25831 |
rs545538863 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139203 | CTTGACTTTTTTTCT[A/C/T]ATGTTTACAATATAG | 25831 |
rs545551963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103690 | AAGTTGATCTTGGCC[A/G]GACAAGGTGGCTCAC | 25831 |
rs545597345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150466 | CCTGGCCTCAGGCAA[G/T]CCTTCCACCTCAACC | 25831 |
rs545621946 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175721 | AATATCAAATTAGCC[A/G]GGCATGGTGGCGCAT | 25831 |
rs545639781 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100124 | CAGTTCTGTACGCTG[C/G]AAACATTTTAATGAT | 25831 |
rs545713158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111560 | CCTGGCTATTTTTTT[A/T]AAACACTATTATGCA | 25831 |
rs545714972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195497 | TCCTTGTATTTTTCC[C/T]GTTGAAACTATTAAG | 25831 |
rs545715176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103366 | GCTAACACAGTGAAA[C/T]CCCGTCTCTACTAAA | 25831 |
rs545750330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157600 | AATGTTAACATGTCA[C/T]GATAATTTTAGAAAA | 25831 |
rs545754859 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174558 | TCAAAAAAAAAATAA[A/T]AAAAATAAAAAATAC | 25831 |
rs545756816 | snp | A/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206656 | AAAGGAAAGGCTAAA[A/T]GTAAATGCAATGGAC | 25831 |
rs545786895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155870 | AATTATACTACAACT[A/C]TGTCCTGGCTTTTTT | 25831 |
rs545794643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112124 | CCCTTAATGTCTACA[A/G]TATCACCTCTCTTTT | 25831 |
rs545801210 | in-del | -/AA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197752 | CCAATTCAATTCTTC[-/AA]AAAAGTTTCCACATG | 25831 |
rs545802441 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202130 | TTTCTACTAAAAATA[A/C]AAAAATTAGCTGGGC | 25831 |
rs545840733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147353 | TAAATAAAAAAGCTA[C/T]GTTCTTTCCAAAGTA | 25831 |
rs545858074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148141 | TACTTTTTTTTAAAA[A/G]TGAAAAAAAAAATGC | 25831 |
rs545885117 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190873 | CCCAGACTGGTCTCC[A/G]ACTCCTGGCCTCAAA | 25831 |
rs545894438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140856 | ATTCAAATGTACACA[A/G]AATAATATAATGAAC | 25831 |
rs545925756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189602 | CCCATCTCTACAAAA[A/T]TTTTAAATAATTAGC | 25831 |
rs545926150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155239 | AATCCCAGCTACGCC[A/G]GAGGCTGAGGCATGA | 25831 |
rs545933240 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167611 | TGGATCAGAGTACTG[A/T]CTAGCAAAAGATGAA | 25831 |
rs545948941 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161188 | TTTCTATTCTGAGAC[A/T]TTTGTGGCTGCAGGT | 25831 |
rs545992119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154497 | GAGATGGGGTTTCAC[A/G]ATGTTGGCCAGGCTG | 25831 |
rs546002875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197033 | CTATGCTTAGCAATG[A/G]GAAAACAAAGACGAG | 25831 |
rs546006561 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161913 | TTCTTCCTATCAAGG[A/T]CTGATAAACATTCAA | 25831 |
rs546022737 | in-del | -/A | 0.131038 | 0.219882 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161580 | GTCTCAAAAAAAAAG[-/A]AAAAAAAAAAAGAAA | 25831 |
rs546023083 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205665 | GTAAACACAAAACTC[-/T]TTCAGGAATATTTTT | 25831 |
rs546036723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201596 | TTCACTGCAACCTCC[A/G]GCTCCCAGGTTCAAG | 25831 |
rs546061131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117068 | CTGTATGAATACTTC[A/G]GAAACATTTTAATTT | 25831 |
rs546100347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125264 | AATGCAACCTCCGCC[C/T]CCCAGGTTCAAAAGA | 25831 |
rs546130247 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112110 | GAACAGTACCCATTC[A/C]CTTAATGTCTACAGT | 25831 |
rs546171520 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151708 | CATGTTTTTTTTTTT[A/T]AAAAAAATGTATAAA | 25831 |
rs546180920 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117450 | TTCTGGGCCAATGAC[A/C/G]TGTCAACCTTTTATC | 25831 |
rs546199292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154075 | CCTTCTACGCTGCTC[C/T]TTTTCCAGGTTGCTT | 25831 |
rs546212401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197802 | ACTCACTCCTCAACC[C/T]ATTCAGATCTGCCCC | 25831 |
rs546225722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168113 | CTAGTAATCTTTTCT[A/G]AAACTTCTCTTCGTT | 25831 |
rs546264519 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209509 | CGAAATGCTGCAATA[A/G]TGGAGGAAAGAAAAG | 25831 |
rs546278381 | snp | C/G/T | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203897 | ATGCTATCCCTCCCC[C/G/T]CTCCCCCTACCCCAC | 25831 |
rs546307388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111824 | TTGTTTGTTTACAAC[A/C]ATGCCATTAGCCACG | 25831 |
rs546341610 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204355 | TTGAACTAGTTTACA[A/G]TCAGTCCCACCAACA | 25831 |
rs546399107 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31210038 | TTTTTTTTTTTTTTT[G/T]TTGAGACGGAGTCTC | 25831 |
rs546406475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31123558 | ATCTCTTGCCTTCGA[C/T]GGAGACTGGGTCAAA | 25831 |
rs546426588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118519 | TGAAGAAATTCAAGC[C/T]TGGATAGTTTTGGTG | 25831 |
rs546438943 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126615 | CTTCTTTTGTGACAA[A/C]ATACAAAAAAAAATG | 25831 |
rs546454670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131289 | TAAAACGAACAAACA[A/C]ACAAAAAACACTCAA | 25831 |
rs546464407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203385 | ACTGGTACACTACCC[C/G]AAACACGGCTAACCC | 25831 |
rs546570988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188543 | CCGGCCTTGTTATTC[C/T]TTCTATCTCAGCCTA | 25831 |
rs546588038 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161391 | AAGACCAGCCTTGGG[C/T]AGCAAAGCAAAACTA | 25831 |
rs546592790 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131896 | CAATAATAGTTGATA[C/T]CTCAACTATTACTGG | 25831 |
rs546608899 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180196 | ATCTGTATGAATGTT[-/A]AAAGTATATCTAATT | 25831 |
rs546658572 | snp | A/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202871 | TAAGGCAGGTGGATC[A/G]GGAGATCAAGAGATG | 25831 |
rs546727794 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167928 | ACATCCTTACTAGCC[C/T]GCAAGGGGAAGAGTA | 25831 |
rs546737415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132633 | TGAAGAAAATAATTA[G/T]CCACTATAATTGCTT | 25831 |
rs546738689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182367 | GCTAGTTTTTAAAAA[A/T]TTTTTTGTAGAGATG | 25831 |
rs546767198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183039 | ATTATCTCTTTAATA[C/T]GAAAACTTAACTAAA | 25831 |
rs546776299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147773 | AAAAAACATTACAAG[C/G]GTTTCACTAAGTTTG | 25831 |
rs546780580 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174037 | GATATTAATGGTACC[G/T]ATATCTCATTGTGTT | 25831 |
rs546787235 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131901 | ATAGTTGATATCTCA[A/G]CTATTACTGGTATTT | 25831 |
rs546806605 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161019 | TGTTTCCTCTTGAAC[A/T]CTGTGCCTTAATTTC | 25831 |
rs546879094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188937 | ACCCACCTGCCCCCA[A/G]CTTTCCCACAACACA | 25831 |
rs546916238 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118314 | CCAGCCTAATACTAT[A/C]AGGCTAAAAAATACA | 25831 |
rs546917598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181879 | TATCAAGGTTTCAAG[A/G]AAAATCAAAGAATGT | 25831 |
rs546945032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103916 | AGGTTGCAGTGAGCC[A/G]AGTTCGTGCCATCAC | 25831 |
rs546953960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179940 | TTGCACTTTGGGAGG[C/G]TGAGGCAGGTGGATC | 25831 |
rs546958650 | in-del | -/ATT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156744 | TTATTTCATATTGTC[-/ATT]ATCCTGTCAAAAACC | 25831 |
rs546987849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125674 | ACGTTTAATAAGCAG[A/C]AACAGAAATATAATG | 25831 |
rs547140829 | in-del | -/T | 0.347914 | 0.230028 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208929 | CCAAAATACTGGTTC[-/T]TTTTTTTTCTTTCTT | 25831 |
rs547155054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150995 | TAGCTACTGGAGAAG[C/T]TGAAGCACGAAGACT | 25831 |
rs547178497 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187266 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACC | 25831 |
rs547186704 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195249 | CAATTAAAATACACA[C/T]ACAAATTTGACTGCA | 25831 |
rs547191859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151826 | ATCTAAATACGTCCA[G/T]CATAAACAACTAAAA | 25831 |
rs547202335 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177315 | AGTTCAGGACCAGCC[C/T]GGCCAACACAGTGAA | 25831 |
rs547205192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159726 | CTCACTGCAACCTCC[A/G]ACTCCCAGGTTCAAG | 25831 |
rs547331618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196612 | TACAAAAATTGGCTG[C/G]GCATGGTGGTGTGCG | 25831 |
rs547336020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157798 | AAAAACTAGCTAGAC[A/G]TGGTGGCAGGCACCT | 25831 |
rs547336878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114721 | TTATTACAAAGAAAG[C/T]ATGTATCAAATCTAG | 25831 |
rs547361846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31164752 | TACCTGGGAAAATTT[A/G]GCATCAAATTTTCTA | 25831 |
rs547375970 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108155 | GGAGTGCAGTGGCAC[A/G]ATCTCAGCTCACTGC | 25831 |
rs547429166 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129209 | TGGCCACGCTACACA[C/T]AGAACTGCTGCTTCC | 25831 |
rs547434954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137277 | TTGGGATTACAGGTG[C/T]GTGCCACCACGCCCG | 25831 |
rs547440556 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200945 | CAATTATCTGTTTTC[C/G]CTATTAGACTATTAG | 25831 |
rs547460950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186558 | ATAGGCGTGGTGGCA[C/T]GTGTCTGTTATCCCA | 25831 |
rs547501239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201711 | GATGGGGTTTCACCA[C/T]GTTTGCCAGGCTGGT | 25831 |
rs547507895 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136882 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGTTCAC | 25831 |
rs547538652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110290 | TTACAGGCATGAGCC[A/G]CCACACCCGGCCACA | 25831 |
rs547560414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159340 | TTTTTAATTTAATTT[A/T]ATTTATTTATTTTTT | 25831 |
rs547572186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143370 | AGTGAGTCAGGACTG[C/T]GCCACTGCACTCAAG | 25831 |
rs547598573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192819 | CGTTTCTACTAAAAA[C/T]GCAAAAAATTAGCCG | 25831 |
rs547642462 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200374 | TTCTTGGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 25831 |
rs547643727 | in-del | -/AAC | 0.267987 | 0.249352 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136027 | GTCTCAAAACAAAAC[-/AAC]AACAACAACAAAAAC | 25831 |
rs547644719 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31150349 | ATAATACTCAATTGC[C/T]TGTAGCTTAATCTTT | 25831 |
rs547650634 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101442 | TCCTCACACCAGAAC[A/G]ACAACACATCTAGAG | 25831 |
rs547666776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206667 | TAAAAGTAAATGCAA[C/T]GGACCAGCAGGTTAC | 25831 |
rs547701254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116056 | ATAGACTGTAAATGT[C/T]CTTCTACTTCTAAAA | 25831 |
rs547723906 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172653 | TGGAGATTCACAAGG[C/T]TTTAAGTCTTAAAAA | 25831 |
rs547750411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172863 | CATTATTATAATTCA[C/T]TCACATCAGTTCCTA | 25831 |
rs547776290 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153205 | AGACCATCCTGGCTA[A/C]CACGGTAAAACCCTG | 25831 |
rs547778199 | snp | A/G | 1.6591e-05 | 0.00288015 | missense | HECTD1 | GRCh38.p7 | 14:31116416 | GCTAATCGAGGTGAC[A/G]GAGTACATTCGACTT | 25831 |
rs547823681 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208571 | AAAAATTAATACGAC[A/T]TGATAGTGTTTGAGA | 25831 |
rs547826403 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186104 | ATCTCTTTAATTACC[A/T]TTTTAATGGATTTCA | 25831 |
rs547836497 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161682 | CAGCACTTTGGGAGG[-/C]CAAGGCAGGCAGATC | 25831 |
rs547842701 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137753 | TTGAAAAGAAAAAAA[A/G]AAAAAAAAGAAAACA | 25831 |
rs547872095 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111263 | TTATCTTTATTTTTT[A/T]TTTTTTTGAGATGGA | 25831 |
rs547875651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130182 | ATTCATATATTGCCA[C/T]AGAAATTTTAGTCAC | 25831 |
rs547910331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122619 | AGCCAGGACTACAAA[C/T]GTCAAAGTGTGGGAC | 25831 |
rs547914337 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153263 | CGGGCATTGTGGCGG[C/G]CGCCTGTAGTCCCAG | 25831 |
rs547915955 | snp | C/T | 1.73438e-05 | 0.00294476 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113853 | CATTTGCAATCAAAA[C/T]AGTGTTTTGATGCCA | 25831 |
rs547963229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115437 | ATAACATTTACTGAG[C/T]ACTTAATATATCCTA | 25831 |
rs547976660 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181173 | TAAAAACTGTACATC[-/A]AAAAAAAAATAAAAT | 25831 |
rs547984139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180943 | ATGCTCTATATATGC[A/G]TATGTAGTAGATGGA | 25831 |
rs547998040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122537 | CTGGAGTGCAGTGAT[A/G]CAATTATAGCTCACT | 25831 |
rs548060712 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130116 | TTTTTTTCTACAAAA[A/C]CATGCCAGCTTACCA | 25831 |
rs548092670 | in-del | -/A | 0.221141 | 0.248329 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183078 | ACACACAAAAAAGGT[-/A]AAAAAAAAATCCCAG | 25831 |
rs548153675 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108842 | CCCTGTGACAGGAGA[C/G/T]GTATTTCCACTCTTC | 25831 |
rs548230741 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129305 | TCCATGATTGCGTTG[C/T]GCCTGAAACAGTGGA | 25831 |
rs548234707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151858 | ATAGACAAGATATAC[A/G]AAAAATGTGTTTTCA | 25831 |
rs548258969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180054 | ATAGTGGCAAGCACC[A/T]GTAATCCCAGCTACT | 25831 |
rs548299437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188631 | TTTTTCTCTTTAGAA[A/T]TTATATTTTATTTCT | 25831 |
rs548372706 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134216 | AGAAGCTCCTCTCAT[A/T]CCATATCAAATGCCA | 25831 |
rs548432199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194111 | ATGAATCTCAAATGC[G/T]ATATGCTAAGTGAAA | 25831 |
rs548435907 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155935 | GTATTCACCTTACCA[C/T]CAATTTTTTTTTTTT | 25831 |
rs548443925 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188947 | CCCCAACTTTCCCAC[A/T]ACACAAACAACTGAA | 25831 |
rs548446887 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101544 | ATACCTGTAATCCCA[A/G]CACCTTGGGAGGCTG | 25831 |
rs548453901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166097 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 25831 |
rs548506678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153260 | AGCCGGGCATTGTGG[C/T]GGGCGCCTGTAGTCC | 25831 |
rs548511962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166929 | TACAATCCCAACACT[C/T]TGGGAGGCCAAAGCA | 25831 |
rs548513300 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180577 | AACCTCCAGGGTAGC[C/T]AGGATTACAGGCACA | 25831 |
rs548546962 | snp | A/G | 0.000798881 | 0.01997 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146925 | AAACAAGGTGAAAAA[A/G]TGTTGTCACAACAGG | 25831 |
rs548574381 | in-del | -/A | 0.35809 | 0.225425 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191845 | CTCTGCTAAAAATAC[-/A]AAAAAAAAAAAAAAT | 25831 |
rs548587666 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178807 | AAACTCTGTTTCAAA[-/G]AAAAAAAAAAAAAAA | 25831 |
rs548594316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192096 | ACTTTGGGACACTGA[C/G]ACAGGTGGATCACCT | 25831 |
rs548618393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198218 | AATGGGAATTAATTA[C/T]AAAGCACTGCATACG | 25831 |
rs548623638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139396 | TTGTTCATCCCTTCT[A/T]CAATGTGAGAACACA | 25831 |
rs548682033 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103852 | CATGCCTATAATCCC[A/G]GCTACTCGGGAGGCT | 25831 |
rs548710520 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153867 | TATATGTGGTAAGGG[G/T]TGAGGTTTAATTATT | 25831 |
rs548713672 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207922 | CCCCGGAGCTCTCGC[A/C]CCCGCCGCCTCGGGC | 25831 |
rs548747388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146122 | GATATTCCAAAAAAC[C/T]CTTGAGGTAGGTGAT | 25831 |
rs548762065 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161094 | TTGTAAATACCCTTT[C/G]TATATAATAAAGACA | 25831 |
rs548808379 | snp | A/G | 1.72086e-05 | 0.00293326 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106614 | AAAACTTATTCATGC[A/G]TTGGATTGAAGAATG | 25831 |
rs548830981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156647 | GATATTCTTTAACTA[C/T]ATTTGCAACATTTCT | 25831 |
rs548841598 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168969 | GAATGACGTAAACCC[A/G]GGAGGCGGAGCTTGC | 25831 |
rs548841650 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176930 | AGACAGAGCAAGACT[A/C]TCTCTCAAAAAAAAA | 25831 |
rs548844281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111339 | CTCACTGCAAGCTCC[A/G]CTTCCCAGGTTCACG | 25831 |
rs548898184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113019 | GGAAGGGAAAGATGG[A/T]GAGAGGTAGAAAAGA | 25831 |
rs548903630 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169578 | AAGCAGGTGGCAATC[C/T]ATATCTCTGCCTTTG | 25831 |
rs548908749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116776 | GCTGGGATTATAGGT[A/G]CCCAACACCACATCT | 25831 |
rs548914069 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114467 | CTGAACACTGAACTC[-/AAG]GAGGATTCTTTTTTT | 25831 |
rs548959392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126257 | GTACATCAAAGCTGG[C/T]TGTCTGGTAGGTGGG | 25831 |
rs548986620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149944 | TAGCAAAAATATGAG[A/G]AAAAAACCAAACTGT | 25831 |
rs548988761 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196481 | AGGTACAGGTCGGGC[A/G]CAGTGGCTCACACCT | 25831 |
rs549009172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171764 | TAAGGGGGAATGAAG[G/T]GGATGGAGATGGCAT | 25831 |
rs549110635 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203807 | TCAACGTGCAGGTTT[G/T]TTACATATGTATACA | 25831 |
rs549124625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158401 | GCTGGGACTACAGGC[A/G]CACACCGCCACGCTC | 25831 |
rs549147014 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207354 | GCCCTTCCGACGGTC[C/G]GAGGCGCTCCCGCCT | 25831 |
rs549176413 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174173 | CTGAAAATAACATCT[-/G]AACAATAAAAAGTCA | 25831 |
rs549227901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113614 | AATAAAAACATAACA[C/T]AAGACATAAATCAAG | 25831 |
rs549252624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119108 | CCTGTTTCCTTAGTC[A/C]CATGTTCTTCTCTGT | 25831 |
rs549254810 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192219 | GGTGTGGTCTTGAGC[A/G]CCTGTAATCCGCTGA | 25831 |
rs549320316 | in-del | -/AT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171668 | AAAAGGAGGGAACAC[-/AT]ATATATATATATTTG | 25831 |
rs549325856 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178968 | ATTTCCTTATTCACT[G/T]AAAATCCCAGAAGGC | 25831 |
rs549346055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206789 | AAGCAACCCCAACAG[C/G]TAAGTCATTACAAAA | 25831 |
rs549347333 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128120 | CACACTAATAATAAA[A/C]TGGTTCCTGAAAAGC | 25831 |
rs549403455 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186454 | GCACTTTGGGAGGCC[A/G]AGCCGGGTGGATCAC | 25831 |
rs549412734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186291 | CTGATGTGTGCCTCT[A/G]TTCCCAAATCTCCAT | 25831 |
rs549422297 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192150 | CAGGAGTTCAAGATC[A/G]GCCTGGACAAGTTGG | 25831 |
rs549478466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171004 | ATTACAGACACCTAG[C/T]TCATACATTTGATGT | 25831 |
rs549489310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192732 | TATAATCTCAGCACT[C/T]TGGGAGGCCAAGGCA | 25831 |
rs549518571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179903 | GTATGAGGCCAGGCC[C/T]GGTGGCTCACGCCTG | 25831 |
rs549541447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31164846 | TTACATGGTAGCATA[C/T]TTTATAATTTTCTGA | 25831 |
rs549558571 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103756 | GCAGATCACCTGAGG[A/G]TGGGAGTTCGAGACC | 25831 |
rs549568000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170326 | TTCTATAGTGACTCC[A/G]GAGGCTGAGGCAGGA | 25831 |
rs549613501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135403 | AGAGTGCTAACAATT[C/T]TATTCTACTTCCTAG | 25831 |
rs549656494 | snp | A/G | 5.05506e-05 | 0.0050272 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178005 | ATAAGTAATGAGCCA[A/G]TAAGTAATACTTACC | 25831 |
rs549670453 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176390 | TTTTTCATTAACCTG[C/T]TATGTATAACATGTA | 25831 |
rs549708449 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156196 | AGCTGGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 25831 |
rs549746453 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160820 | GGACTACAGGTATGC[A/G]CCACCATACTCAGCT | 25831 |
rs549748852 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207947 | TCGGGCTGTGTCGTA[C/T]GTTTCTGCCGCGGCT | 25831 |
rs549778514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204934 | ATTAGGATAATTATA[C/G]CAAATTTTTTAGGTC | 25831 |
rs549782596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120366 | TCTGTACTCCACCCC[A/G]GGAGACAGAGTGAGG | 25831 |
rs549812768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102120 | CTACATGATTTCATA[C/T]ATTAAAAGTTCAAAA | 25831 |
rs549832369 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100397 | AAGTTTGGTGCATGA[C/T]TATATGCCAAACAAA | 25831 |
rs549833378 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207431 | CGATCCAGCTCCCAA[C/T]AGGCCGCCGGCAGAG | 25831 |
rs549859343 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31173036 | CACAGGGATAGGGGA[A/G]AATATCGAAGGGGTG | 25831 |
rs549874395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109251 | TGAAAAAGATGCTCT[A/G]CCAGAGGAGAAGGCT | 25831 |
rs549913432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152552 | TCATCACATTTACAA[A/T]ATCCAGTAGCAAATC | 25831 |
rs549979083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115338 | GTGATGTTAAGAGAA[C/T]ATCAGAAAACATACT | 25831 |
rs549994351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198942 | TCAGGAGGCTAAGGC[A/G]GGAGAACTGCTTGAA | 25831 |
rs550034855 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133119 | CTTTTTTCCATTTGT[A/T]ATGTGGTATCAACAG | 25831 |
rs550048862 | snp | A/G | 0.00011665 | 0.00763619 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31106879 | GGGTTTTGGTTTAGG[A/G]GGATCAAGAATAAAT | 25831 |
rs550055601 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165015 | AAAAAAAAAAAAAAA[-/A]GTGACCCCACTAACA | 25831 |
rs550073756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113656 | CATTAAAATTCCCAA[A/G]TAAAATATAACCACT | 25831 |
rs550083357 | in-del | -/AGG | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192946 | ACACCACTGCACTCC[-/AGG]AGCCTGGCGGCAGAG | 25831 |
rs550129999 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200461 | GATCAGCCTGGGGAA[A/C]CTAGTGAGACCTTGT | 25831 |
rs550143011 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122154 | CTGTGTGTGTGCTTG[G/T]GTGTGTGTGTGTCAG | 25831 |
rs550154474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144500 | TCAACCACGCCCCTG[A/T]AGCACCAAAGTAGTC | 25831 |
rs550181761 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145669 | TTTGCCTCAAAAAAT[-/A]AAAAAAAAATAAATA | 25831 |
rs550193060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193603 | CAATTTCTACATCTT[A/G]TTGAATTTATCTCCA | 25831 |
rs550214715 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179846 | TCTTAGTGTATGCAA[A/T]TGAGTACTTCCCATA | 25831 |
rs550276104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154791 | CTCTCTCTTTCACCA[A/C]CCTCGGGATTCTACA | 25831 |
rs550291608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203548 | CGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGC | 25831 |
rs550344251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158529 | CCTCCCAGAGTGCTG[A/G]GATTACAGGCGTGAG | 25831 |
rs550353013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196733 | CACTCCAGCCTACAC[A/G]ACAGAGCAAGACTCC | 25831 |
rs550368986 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165020 | AAAAAAAAAAAGTGA[A/C]CCCACTAACACCTAC | 25831 |
rs550393312 | snp | C/T | 1.656e-05 | 0.00287745 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129185 | AACCCAAGCTGATGT[C/T]GCTGCTACTGGCCAC | 25831 |
rs550443484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179007 | CTGCTCAATTCATAT[G/T]TTTCAGAAAGAAGCA | 25831 |
rs550456663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128283 | CAAAAGCTATACTTA[C/T]ATGATGCTTTGGTTT | 25831 |
rs550457647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171106 | TAGTCTGAGTCTAGT[G/T]ATTCTTCTACAAACA | 25831 |
rs550467973 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104047 | GGAATGTTGCATGTG[A/G]GGGTGGATGAAGAGA | 25831 |
rs550551648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162226 | TGACAGAGCAAGACT[C/G]TCTCAAAAAAAAAAA | 25831 |
rs550692903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135855 | AAACCCCGTTTCTAC[C/T]AAAAATACAAAAATT | 25831 |
rs550743176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140976 | TCTGTCACCTAGGCT[C/G]GAGTACGGTGGCTCA | 25831 |
rs550758806 | in-del | -/AA | 0.0146672 | 0.084371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174729 | CACACTTATAATCTT[-/AA]AAGTTTCATTCCCAA | 25831 |
rs550782555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125048 | CCTGACCTTGTGATC[C/T]GCCCACCTTGGCCTC | 25831 |
rs550783674 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133808 | TTAACTCAACAGTTC[A/G]TTACAAGAATCAAGA | 25831 |
rs550783840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141454 | GATCAGGCTAGGAAC[A/G]GTGGTTCATGCCTAT | 25831 |
rs550795034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132432 | ACAAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 25831 |
rs550845376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105227 | GCTGGTCTCGAACTC[C/G]CAACCTCAGGTGATC | 25831 |
rs550923856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169707 | CCAACCTGGAGAAAC[C/T]CCGTCTCTACTAAAA | 25831 |
rs550925459 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125261 | CTCAATGCAACCTCC[A/G]CCTCCCAGGTTCAAA | 25831 |
rs550973520 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195768 | ATCAGGTGATCCACC[C/T]GCCCTGGCCTCCCAT | 25831 |
rs550989302 | snp | C/T | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119838 | CATGTTCTCCGGCGT[C/T]CTCCTTTAGTTTCGT | 25831 |
rs551000470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106022 | TTTGCAATGAATTAT[C/G]ACAGCAACATGTTTG | 25831 |
rs551018726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204150 | CAGTCTATCATCGAT[C/T]GACATTTGGGTTGGT | 25831 |
rs551061761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105292 | AGGTGTGAGCCACCG[C/T]GCCCAGCCGACCACC | 25831 |
rs551092040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141052 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 25831 |
rs551092975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185070 | GCTTCTGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 25831 |
rs551161019 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168538 | CAAGGAAAAAAACCT[G/T]AAGATATATCCAACT | 25831 |
rs551189993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113545 | AAAAACAGTGTATCA[C/T]TGTATCAATACCACT | 25831 |
rs551215251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197278 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 25831 |
rs551230650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191357 | ACAGCAAAACTCTGT[C/G]TCTACAATAAATACA | 25831 |
rs551232425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184343 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCGAGC | 25831 |
rs551262426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175526 | AGCCATTATCGCCCA[C/T]TGCATTCCCATCCTG | 25831 |
rs551302806 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148428 | TATCCTAGTATCATT[A/T]ATAATCTCAATGAGT | 25831 |
rs551302926 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198097 | AGCACTGGTATTAAG[-/A]AAAAAAGCCAGTTTC | 25831 |
rs551312521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112342 | TATCAGTCTTGACAG[C/T]ATAGTTGTACATTTT | 25831 |
rs551353423 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198375 | TCAAAATTTAATCAC[A/G]TATGCCTTTCATTTC | 25831 |
rs551380372 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180293 | AAAATTTTAGGGCCC[A/G]TATGGCGGCTCACAC | 25831 |
rs551386764 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198090 | CACTGCCAAGCACTG[G/T]TATTAAGAAAAAAGC | 25831 |
rs551396462 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168412 | TTACATTCTTCTTCA[C/T]CTTTGTTTGTATCTT | 25831 |
rs551424783 | in-del | -/AACAAC | 0.0243523 | 0.107625 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136024 | TCTGTCTCAAAACAA[-/AACAAC]AACAACAACAAAAAC | 25831 |
rs551458099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170850 | TGCTAAGAATATATA[C/T]TTATTTTATAGACAA | 25831 |
rs551509672 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175635 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACTTGAG | 25831 |
rs551521245 | in-del | -/GGCG | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149629 | ATATTTTTGTTTCTA[-/GGCG]CAGTGGCTCACACCT | 25831 |
rs551527920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168904 | AAAAAATTAGCTGGG[C/T]ACGGTGGCGGGTGCC | 25831 |
rs551548829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155516 | TAGTATCACCTCTAT[A/G]GGACTTTTGCTAAAA | 25831 |
rs551618006 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128653 | AAAGTATTAGTGTTG[G/T]TATCACTGCTGCTTC | 25831 |
rs551653285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125102 | TGAGCCACTGTGCCC[A/G]GCCAACAATAAATTT | 25831 |
rs551657049 | snp | A/G/T | 0.000184347 | 0.00959905 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133257 | GTGTAGTTCTCCTGT[A/G/T]ACAGTGCCTTCTCCC | 25831 |
rs551699307 | snp | A/G | 0.000132694 | 0.00814429 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135156 | TGACGTTACTACTAC[A/G]AGTCCATAGGCAGCT | 25831 |
rs551727434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164218 | TGCACAGGCCTACAC[A/C]GGTAATAGCTAATGT | 25831 |
rs551807912 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192025 | AAAAAAAAGAAAGAA[A/G]GAAAGAAAAACAGAG | 25831 |
rs551808966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131165 | GCCATGTTGATTAGG[C/T]AAAACTAAATTTCTA | 25831 |
rs551815502 | snp | C/G | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099734 | ATACAGTCCCTTCTT[C/G]AAAACCAGAAAACAG | 25831 |
rs551824402 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132676 | CAATTTATTAAGTGG[A/T]TGACTTTGCTAAACT | 25831 |
rs551829271 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117194 | GCCTGGGTAACACAG[A/T]GAACCCCGTCTCTAC | 25831 |
rs551913526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116819 | TATTTTTAGTAGAGA[C/T]GGCAGGTTTCACCAT | 25831 |
rs551969752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130258 | AAGTTCAGTGGTTCC[C/T]TGGTTCTCTTATATT | 25831 |
rs551970063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138457 | TCCTCTCTTTGGATC[C/T]TGCACAATCTCCTGA | 25831 |
rs551997582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173916 | AGCAAAGTGATTAAG[C/G]ATGTGATCTGCCTAT | 25831 |
rs552010079 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191486 | TGAGCCAAGATGACA[A/C]CACTGCACTCCAGCC | 25831 |
rs552025622 | in-del | -/AATTCAGAT | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183574 | AAGTGAACAATGTTA[-/AATTCAGAT]AATTCAGTCTTCAGA | 25831 |
rs552083055 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31168813 | TTTGGGAGGCCGAGA[C/T]GGGCGGATCACGAGG | 25831 |
rs552083078 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203209 | TGATGCCACAGCCCA[C/T]TCTTTCCATCTCACT | 25831 |
rs552094378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141490 | CAACACGTTGGGCAG[C/T]GAAGACAGGAGAAAT | 25831 |
rs552144387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171320 | GGGAGGCTGAGGCAC[A/G]AGATCGTTTGAACAC | 25831 |
rs552202900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122738 | TAAGCAACTTATTTT[C/T]TTTAAGTGGAGAATC | 25831 |
rs552232477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145249 | TGCAACAGAAAAAAA[C/T]GTATCTCTCTAAACT | 25831 |
rs552232911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192834 | CGCAAAAAATTAGCC[A/G]GGTGTGGTGACAGGC | 25831 |
rs552276070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182511 | ATTCCTATTAAACTA[G/T]TTACATGATAATGAG | 25831 |
rs552284989 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31121828 | AAATTTTAAATTTAC[A/G]GTTAGTTACAATAAA | 25831 |
rs552291858 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125586 | GGCCACCATGAGAAA[C/T]AATAAATCAGAAAAC | 25831 |
rs552319019 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153968 | GAAAATCAATTGGCC[A/C/G]TATGTGTAGTGGGTC | 25831 |
rs552371909 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189878 | TGATAGTCTTCCCTA[C/T]GAGAGGGCCTGAGTT | 25831 |
rs552425887 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183955 | TCCAGCAATCTTCCC[A/T]TCTCGGACTCCTAAA | 25831 |
rs552430685 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160452 | TAACAGCCTAAACAC[C/T]TTCATTAAGTATTGA | 25831 |
rs552438393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181013 | AAAAACACAGTCTAA[A/G]AGAGTAATGTGTTTT | 25831 |
rs552480696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153317 | GAATGGCTTGAATCC[A/G]GGAGGCAGAGCTAGC | 25831 |
rs552485396 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31150770 | GTATCCAAAGTGAAG[C/T]GTGTAACAGAATCAC | 25831 |
rs552500858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147087 | GAGGCCGAGGCAGGT[A/G]GATCACTTGAGGTCA | 25831 |
rs552520550 | snp | A/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187991 | AAACTCCAGACCTCA[A/G]GTGATCTGCCCACCT | 25831 |
rs552524525 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140282 | TATTTGATAAATAAA[A/T]AAGAATATAAAGCAA | 25831 |
rs552541532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195834 | CCTGGCCTCTACATT[G/T]TTTTAGCTGACAGAA | 25831 |
rs552596579 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196537 | AGGCGGGAGGATCAC[C/G]AGGTCAGGAGTTCGA | 25831 |
rs552603599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116891 | GCCCGTCTCAGACTC[C/T]TGAAGTGCTGGGATT | 25831 |
rs552614766 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131670 | AAGATTCTAATTTCC[C/G]TATGCAATTGCTTCA | 25831 |
rs552660853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189944 | GTGAAAGTGACCACT[A/G]TGTGACTTCAAATGC | 25831 |
rs552685686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152909 | GAGAATTGCTTGAAC[A/C]CGGGAGGCAGAGGTT | 25831 |
rs552688147 | snp | C/T | 0.000152733 | 0.00873745 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103090 | TACATGTAACGGAAA[C/T]ACAAAAAACAAACAT | 25831 |
rs552690853 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104526 | CAGTCTGGAGTTCAC[C/T]AGCTCTTTCTGTCAT | 25831 |
rs552793934 | snp | A/G | 0.000335542 | 0.0129483 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101330 | GAAACCAGGGCTAAA[A/G]GAACAAAAATATAGT | 25831 |
rs552807891 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122427 | TCAGGTTGGAGTGCA[A/G]TGATGCAATTATAGC | 25831 |
rs552854303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103871 | ACTCGGGAGGCTGAA[A/G]CAGGAAAATCGCCTG | 25831 |
rs552857825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166389 | AGAAAGAAGGCTAGC[A/G]TAAGTGTAATGGGCC | 25831 |
rs552872982 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209318 | AGTAAGCAACAGAGA[A/G]AGAAATTTGGAGCTA | 25831 |
rs552892766 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208243 | CGACCGCCTGGCGGT[C/T]CACCCCAAAGAAAAC | 25831 |
rs552915762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111794 | ACATTAATTCTCTTG[A/G]TAAGAATCTTGCCCT | 25831 |
rs552915915 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103450 | GGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAATC | 25831 |
rs552970514 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114743 | CAAATCTAGAACTTT[C/T]AAAGATATGACTGTA | 25831 |
rs552980916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201956 | AAGAAGTTATATTCG[C/T]TGAACTTCAGAAAGA | 25831 |
rs552981323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194625 | CTATTTAGGAAACTT[G/T]AGGATCAATCAGTCT | 25831 |
rs553010335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167109 | CCCAGGAGTTCAAGG[C/T]TACAGTGAGCTATGA | 25831 |
rs553068842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201402 | TTTAGTAGCAAGATC[C/T]AGAAATGCCCATAAT | 25831 |
rs553125536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112013 | AACAAAAACAAAAAA[A/T]CAGCAATGCCAACAG | 25831 |
rs553237076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165891 | TGCTCTGTTGCCTAG[A/G]CTGGAATGCAGTGGC | 25831 |
rs553277229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131646 | CCATTGTATCTTGGG[A/G]AAAAAAAAAAGATTC | 25831 |
rs553296169 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172370 | GCACTCTGGGAGGCC[A/G]AGGTGGGAGGAGGTC | 25831 |
rs553298874 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158922 | GCACTCCAGCCTGGA[C/T]GACAGAGCCAGACTC | 25831 |
rs553299443 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31123654 | ACTAAAGGGATTATA[A/G]CAGAAGTTTTTACTG | 25831 |
rs553342594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188833 | AATGAACTCCACCAC[A/C]CATGCCCAATCCCTC | 25831 |
rs553399734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125204 | TTTGAGACAGAGTCT[C/T]GCCCTGTTGCCCAGG | 25831 |
rs553410924 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125848 | TAAAATTACTCCCAA[-/T]TTTTTTTTTTTTAAA | 25831 |
rs553436600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118243 | AACTCCTGACCTTGT[A/G]ATCCACTCGCCTCAG | 25831 |
rs553439142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138949 | AGGACATTAGTAAAA[C/T]GTATTGTTTGTTTGC | 25831 |
rs553462890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124689 | TCACCATTTGAGTGA[C/T]AAGATCAATAGAAGT | 25831 |
rs553494359 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104706 | GAGGCAAGGTCTCCC[G/T]CTGTTGCCCAGGCTG | 25831 |
rs553503197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174459 | CTGAGGCAGGACAAT[C/T]GCTTGAACCCGGGAG | 25831 |
rs553554071 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132211 | GGGAGGCCGAGGTGG[A/G]TGGATCACCTGAGGT | 25831 |
rs553576772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177514 | TGTCTCAAAAACAAT[A/G]ATAATAATAATAATA | 25831 |
rs553629908 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104592 | GTAATTTACCTTGTA[A/C]TATACTTTGTTCCCA | 25831 |
rs553638743 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205140 | AAGTTATGACTTATA[C/T]AAGAGGGAAAAAAAT | 25831 |
rs553694363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164502 | TATCACTTTTCAAAT[A/G]CCTCTAACATTGTAG | 25831 |
rs553812820 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101783 | GACAATAAGAGCGAA[A/T]CTCCATCTCAAAAAT | 25831 |
rs553814787 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102331 | TAATATAAACGTAGT[A/G]TATAGCCCAACAGCT | 25831 |
rs553896328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134780 | ATTTTGCTTCAATAT[C/T]TCACAAGGAAGAGAG | 25831 |
rs553896859 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201825 | ATGTTTACATTACTA[C/T]ATTTTAGAACTCGAT | 25831 |
rs553900902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129701 | CAAGAAATATGTACT[C/T]TATACAAGGTTTCCA | 25831 |
rs553924629 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207576 | TGGTGACAGGGAAGC[A/G]AGAGGTTCTCGCGTG | 25831 |
rs553926282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200226 | TATATTCAACTTTCT[A/G]CTTTTATCACAAAAC | 25831 |
rs553928529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193690 | GCACTTTGGGAGGCT[A/G]AGGCAGGCAGATCAC | 25831 |
rs553945728 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130479 | TTAACTTCCAAAAGC[-/A]AAAAAAAAATTGTCT | 25831 |
rs553951012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138286 | ATAGTTTTTAATCCA[A/G]TACATTTTAGTAAGC | 25831 |
rs553974225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101664 | GGGCGTGGTGGCGCA[C/T]GCCTGTAATCCCAGC | 25831 |
rs553987874 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191755 | TGTAATCCCAGCACT[G/T]TGGGAGGTCGAGGCA | 25831 |
rs554007159 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166547 | CGTGTGATATAATTA[C/T]GATTTAAAGATATAA | 25831 |
rs554008509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206949 | GGGGCCCGGCCGAGC[C/T]GGGCGCTGAGAGGCG | 25831 |
rs554011883 | snp | A/G | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126907 | GTTCCTGAGCCTCAG[A/G]TGATCCTCCCACCTT | 25831 |
rs554063082 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108536 | CTATATTAGAAGAAT[G/T]TAAACAACTGGGCAT | 25831 |
rs554137782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138029 | TACTCCGCTAGAATA[C/T]ATTCTACAGGATAAG | 25831 |
rs554160601 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184708 | TCACGCACAATGCAC[-/T]TTTAGCCTGGGCAAC | 25831 |
rs554162636 | snp | C/T | 0 | 0 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148086 | GTAAAATAAACATAC[C/T]AGTCACCAGAAAATG | 25831 |
rs554224130 | in-del | -/TATC | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151101 | TGTCTCTATTATCTA[-/TATC]TATCTATCTATCTAT | 25831 |
rs554235283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171290 | GATGGCACACGCCTA[C/T]AATCCCAGCCACTTG | 25831 |
rs554249390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165175 | CTGGTATTTGAGGTA[C/T]TTGAATCTTATAAAA | 25831 |
rs554277761 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207600 | TCGCGTGCGGCAGCA[A/G]CCAGCGGACGTCCAG | 25831 |
rs554280216 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102249 | ATACAGGTGTGTTCA[C/T]TTTGACAAAATCCTC | 25831 |
rs554288868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137073 | GTGATCCACCCTTCT[C/T]GGCCTCTCAAAGTGC | 25831 |
rs554292688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158556 | TGAGCCACCACGCCC[A/G]GCCAAATTAACCTCA | 25831 |
rs554297561 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181236 | TTTCATGGGGGAATG[C/T]AGTATTTGCTAATTT | 25831 |
rs554324655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121582 | CAGCCATGACCTGAA[C/T]ATATTAACCCCTATT | 25831 |
rs554325219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136915 | CAAGCTTCACCTCCC[A/G]GGTTCATGCCATTCT | 25831 |
rs554349841 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146809 | AGGGAGCTGAGACTG[C/T]GCCACTGCCCTCCAA | 25831 |
rs554351427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105805 | ATGGCTATCAAAACC[A/G]TAAATCCCACCCCTC | 25831 |
rs554381115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151593 | GAGATGGTGTTTCAC[C/T]GTGTTAGCCAGGATG | 25831 |
rs554382844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193020 | AAACTCACGCAAGCA[C/G]CATTAGATAACCTGG | 25831 |
rs554418213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143621 | CCATCCACAAGACTG[A/G]GTCTGAGTTATTTTT | 25831 |
rs554418343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152159 | TATACGGGGTGATAC[C/T]GCATAAGATTGGGCA | 25831 |
rs554431194 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31140138 | TAGATTATGTCTGAG[C/T]AGAAATACTCTCACA | 25831 |
rs554488547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143432 | AATAAATAAATATAT[A/C]AACAAAGGAAAAAAG | 25831 |
rs554517874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158174 | AAATTAGTATGCCTC[A/C]TTTCCCTTTTATTCA | 25831 |
rs554583073 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108559 | CTGGGCATGGTGGCT[C/T]AAGCCTGTAATCCCA | 25831 |
rs554590248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186602 | CTGAGGCATGAGAAC[C/T]GCCTGAACCCAGGAG | 25831 |
rs554605143 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188118 | AGATAGATAGATAGA[C/T]AGATAGATAGATAGA | 25831 |
rs554649023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130466 | TTTAAAAAGGTAATT[A/C]ACTTCCAAAAGCAAA | 25831 |
rs554689843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122792 | TTTTCTTAATTAACT[A/G]CATTTTTTATACTGG | 25831 |
rs554700082 | snp | A/G | 1.65688e-05 | 0.00287821 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173208 | TTTACTTCGAATACA[A/G]TCTATAAGCTGCCGA | 25831 |
rs554729865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193774 | ACTAAAAATACAAAA[A/C]TTAGCCGGGCATGGT | 25831 |
rs554732173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127427 | CGCGATCTCTGCTCA[C/G]TGTAACCTCCGCCTC | 25831 |
rs554792989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194387 | GTATGTAATTTAAAC[A/C]AATTTAAGAAAAAGT | 25831 |
rs554808222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186049 | ACTCCCCTGGTTTTC[C/T]ACTCTAGCTTCCTTC | 25831 |
rs554864434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192885 | AGGAGACCGAGGCAG[A/G]AGAATCACTTGAACC | 25831 |
rs554884290 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185109 | GCATTTTGGGAGGCC[A/G]AGGAGGACGGATCAT | 25831 |
rs554893734 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135890 | AGGCGTGGTGGCAGG[G/T]GCCTATAGTCCCAGC | 25831 |
rs554937136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200647 | GTAGCCAGGCATGGT[A/G]GCGTGTGCATGTAAT | 25831 |
rs554945412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158761 | CCAGCCTGACCAATA[A/T]GGTGAAACCCCGTCT | 25831 |
rs554968450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131310 | AAACACTCAAAATAT[C/T]CAGATGTACATGTTA | 25831 |
rs554980932 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182038 | AGTTGGGACTACAGG[C/G]ACCTAACACATGCCC | 25831 |
rs555084989 | in-del | -/C | 0.00637825 | 0.056111 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162412 | ACTTAATAAATAGTA[-/C]CCCCTCCCCTGAATG | 25831 |
rs555094889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185211 | GCTGGGTGTGGTGGC[A/G]GGCGCCTGTAGTTCC | 25831 |
rs555115498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152748 | TAAAAAAATAAAGAG[G/T]CCAGGTGCGGTGGAT | 25831 |
rs555128840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196923 | AATACCTTCCATGGG[C/T]ATTTTAGGCATTAGG | 25831 |
rs555129914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201022 | AGACCTAACATAAAG[C/T]AGACAATTTAAAGTT | 25831 |
rs555144741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138177 | AATCGGTAACAAATA[C/T]TATAAAATCCAAAAC | 25831 |
rs555150771 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115127 | AGGATAGAAATAACA[A/G]TGATCAGGAGTGCTT | 25831 |
rs555169467 | snp | A/G | 6.76064e-05 | 0.00581366 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144795 | ATCATTAAAATCTAG[A/G]GGATGACATACTTGT | 25831 |
rs555181856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197506 | TTCTGCATAATCTAG[G/T]ACCATATTAGAAATG | 25831 |
rs555231843 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194480 | CACAAAATTTTATAT[A/G]TAATTACAGTTGCTC | 25831 |
rs555247708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204208 | ACACAATAAACATAC[C/G]TGTGCATGTGTCTTT | 25831 |
rs555298441 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120647 | TTGCTTTAAATTACT[A/G]TGAGGCAGACAGCAT | 25831 |
rs555304505 | snp | A/C | 0.000215305 | 0.0103733 | missense | HECTD1 | GRCh38.p7 | 14:31105443 | AGTCAAACATCAAAT[A/C]CACATATTCTTCTGC | 25831 |
rs555312861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190274 | TCCAGTTTCCAAAAT[C/G]CAGATAATCTGTTAG | 25831 |
rs555328243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134117 | GGACTTAAAAACATT[G/T]TTGCAAACTTTTAAA | 25831 |
rs555345699 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190934 | GCGATTACAGACATG[-/C]CCCCACTGCACCCCA | 25831 |
rs555350212 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142839 | TGTAATCCCAGCACC[C/T]TGGGAGGCCAAGGAA | 25831 |
rs555365184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125886 | AGGCAGTATGATCAA[A/G]GATATATGGTAAAGG | 25831 |
rs555393414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190912 | CCACTTCAGCCTCCC[A/G]AAGTGCTGCGATTAC | 25831 |
rs555410474 | snp | G/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133388 | TCTGCCGTCTAAGAT[G/T]AGCTTCTGCTTCTTT | 25831 |
rs555413392 | snp | C/T | 2.23416e-05 | 0.0033422 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31114340 | TTCTCTGTACATGAT[C/T]CTAAACATGAAGATA | 25831 |
rs555430786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176728 | ATCACCTGAGGTCAG[C/G]AGTTCGAGACCAGCC | 25831 |
rs555445895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150292 | TCATACATATTTTAA[A/G]AACATGAATCTAATT | 25831 |
rs555475167 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149683 | CGAGGTAGGGGGATC[A/T]CCTGAGGTCAGGAGT | 25831 |
rs555488136 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166202 | TATAAAAAGTGTAAC[A/G]GGGTAAATTTAAATC | 25831 |
rs555502703 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209276 | AGACATAGGAAAGGT[C/T]ACCTGTGCCCCCAGC | 25831 |
rs555523316 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100842 | AAGTGTCATTAGCAT[A/G]GTGGATCATATACTT | 25831 |
rs555552197 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206231 | GTTGCTGCTTAACTA[A/G]AAACCAGAGCTGTCT | 25831 |
rs555553767 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183769 | CTAAAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 25831 |
rs555560910 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196702 | GAGGTTACAGTGAGC[A/C]GAGATTGCGCCACTG | 25831 |
rs555586603 | snp | A/T | 0.000425087 | 0.0145727 | missense | HECTD1 | GRCh38.p7 | 14:31107235 | ATCCAGGAGGTTTCA[A/T]TCCACCTCCAAGATC | 25831 |
rs555604037 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146203 | TAAAATTTGTAACCT[C/T]AAAATCAATCATTGC | 25831 |
rs555614026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161748 | CATGGCAAAACCCCA[C/T]TTTTACTAAAAACAC | 25831 |
rs555621662 | snp | A/G | 1.65641e-05 | 0.00287781 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157216 | TATTGTAGGCAAATT[A/G]TGACCAACATCAGAA | 25831 |
rs555642274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104916 | CTCCTGGGCTCAAGC[A/G]ATCCTCCTGCTTCAG | 25831 |
rs555663344 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163693 | GGCAGGCGGATCACT[G/T]GAGGTCAGGAGTTTA | 25831 |
rs555668786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154995 | GTGGGTTAAATTTAC[C/T]GAGGAACAGCATATT | 25831 |
rs555682815 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189259 | AATCTAAGACTTAAT[C/G]TTGTTGGTTCTACCT | 25831 |
rs555733145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204744 | AATGACAAAAACTAA[C/T]GGAAATAAATGGACC | 25831 |
rs555751242 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174672 | CAAGTACAGCTGTAA[A/G]AACATTTTTATGATA | 25831 |
rs555776380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177316 | GTTCAGGACCAGCCC[A/G]GCCAACACAGTGAAA | 25831 |
rs555785507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199177 | CCTTTCCCAAATACA[C/T]CTGTGGATGATTTTT | 25831 |
rs555800419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106401 | CACAGGCATATAAAT[A/T]CACATTGGCTAAGTC | 25831 |
rs555810575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156410 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAATTA | 25831 |
rs555896962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163680 | TTTAGGAGGCAGAGG[C/T]AGGCGGATCACTTGA | 25831 |
rs555921888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191016 | GCTGGAGTACAGTTG[C/T]GCAATCATAACTCCC | 25831 |
rs556053793 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149477 | AGGAGCTATATTTGT[A/G]AAGATATTTTTTAAA | 25831 |
rs556068142 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198278 | GACTGAACTAGCCAC[C/T]TTTTTCTTGCAACAC | 25831 |
rs556078389 | in-del | -/AAAT | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136244 | GGCTATATGATACTC[-/AAAT]TAATAGAAATAATTA | 25831 |
rs556086213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169248 | AATTATTTGACTTCA[C/T]AGGAATAGTTCATTT | 25831 |
rs556103721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126779 | CCTTGAACTTCAGGG[C/T]TCAAGTAACCCTCTC | 25831 |
rs556131638 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099682 | GCACAGATATGGTAA[C/T]AACTGGAATTTGGAA | 25831 |
rs556213850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108370 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCT | 25831 |
rs556213896 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183741 | AAGACAGGGTCCCAC[C/T]CTGTCACCCAAGCTA | 25831 |
rs556221160 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141636 | GTAAACTAAGTGATC[A/G]GCTGCATTCATACCA | 25831 |
rs556249415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177371 | ACAAATTAGCCGGGC[A/G]TGGTGGTGGGCACCT | 25831 |
rs556250146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143568 | CTCATCTGTATTTGT[C/T]GTAACTTTAAGCAGA | 25831 |
rs556275261 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201211 | TTTCCTCTGGGAAGA[C/G]GAACCAAGTAACCAG | 25831 |
rs556299263 | in-del | -/TAG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181039 | GTTTTCTTTAGAAAA[-/TAG]TAGTTTTTTGAATAA | 25831 |
rs556346496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206881 | GTGGGAAGCCGGCGG[C/T]GGGGCGCGGTGGGCA | 25831 |
rs556352099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200135 | ACCTGAGTCATCCAC[A/G]ACACTTCCTTCTCCC | 25831 |
rs556363327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141217 | ACAGGCGTGAGCCAC[C/G]GTGCCTGGCCTACTT | 25831 |
rs556392027 | snp | C/T | 1.65864e-05 | 0.00287974 | synonymous-codon, intron-variant | HECTD1 | GRCh38.p7 | 14:31113925 | GTTTTTCCTAATACT[C/T]TTATTAGTGCCAGTT | 25831 |
rs556396565 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114459 | TGCCTGCACTGAACA[C/T]TGAACTCAAGGAGGA | 25831 |
rs556405113 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155742 | TTCATTGTGGACCAG[A/G]AAAAAAAATTACTAT | 25831 |
rs556411625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151350 | GCCAAGTGAATCAAA[C/T]ATACTCATTCCCATG | 25831 |
rs556469477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105762 | TCTGCCATCAGTGGG[C/T]ACAAGAGAAAAAATT | 25831 |
rs556574094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170562 | AGCTGACTTTAAAAG[C/T]ACTTGAAAGGGAAAC | 25831 |
rs556595092 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100910 | TAAAGTCTCTGATGT[A/C]TCCCATTGCACTTCA | 25831 |
rs556598025 | in-del | -/CTT | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144605 | TGTCTTGAAATTGTC[-/CTT]CTGGTTTGTTTTCAA | 25831 |
rs556612415 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111854 | GCGTGGTGGCGTGCA[A/C]CTGTAATCCCAGCCA | 25831 |
rs556647854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142947 | GAACTGAGTAGTCCA[C/T]GTTTCAGCAGTACAT | 25831 |
rs556677461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157898 | CCATCCTGGGAGACT[A/G]AAGGAGACTCCATCT | 25831 |
rs556704547 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159505 | CCACCACACCCAGCT[A/C]ATTTTTGTAGTTTTA | 25831 |
rs556734408 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186040 | GATTTATGACTCCCC[-/T]TGGTTTTCCACTCTA | 25831 |
rs556737283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117028 | GATAGAGAGCTCTCT[A/C]ATTTTTACATGAAAA | 25831 |
rs556773801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153487 | GTGCTGGGATTACAG[C/G]CATGAGGCATCATGC | 25831 |
rs556808661 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146625 | TTGGGAGGCCAAGGC[A/G]GGCAGATCACTTGAG | 25831 |
rs556835395 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31106578 | ATTGCAAATCAGTGA[C/T]GACAAAGAAACAAAA | 25831 |
rs556886006 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202051 | CGGCACTTTGGGAGG[A/C]TGAGATGGGTGGATC | 25831 |
rs556893951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163781 | CGGGCATGGTGGTGC[A/G]TGCCTGTAATCCCTG | 25831 |
rs556904144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164386 | TAAGCTGGTCTCAAG[A/C]GATCCTACTACCTCA | 25831 |
rs556906938 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162933 | AAAATTAGTCAGGTG[C/T]GGTGGTGCTCGCCTG | 25831 |
rs556923435 | in-del | -/C | 0.00835141 | 0.0640778 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209284 | GAAAGGTCACCTGTG[-/C]CCCCAGCAAAGAACC | 25831 |
rs556938242 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193558 | GCATAAGTCCTTTGC[A/C]TTTCCATATAAATTT | 25831 |
rs556989854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202982 | TTGTCCCAGCTACTC[A/G]GGAGGCTGAAGCAGG | 25831 |
rs557027419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155210 | ATTAGCTGGGCGTGG[C/T]GGTACGTGCCTGTAA | 25831 |
rs557028590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103973 | AACTCCGTCTCAAAA[A/G]AACAAAAACAACAAA | 25831 |
rs557029780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168569 | TCAAATAATAATTAT[A/C]TCTAATTAACAAATA | 25831 |
rs557063088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195386 | TTCAATCTAATGATA[C/T]AGTCAAGAACTATGC | 25831 |
rs557063554 | in-del | -/C | 0.00280055 | 0.0373153 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162412 | CTTAATAAATAGTAC[-/C]CCCCTCCCCTGAATG | 25831 |
rs557075234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160784 | CAAACAATCCTCCCA[A/C]CTCAGCCTCTCGAGT | 25831 |
rs557115690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132905 | ACCATAAAAATTATG[C/G]TGTGAGACTAACAAG | 25831 |
rs557123117 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209585 | TTTGAAAGAAGATAT[A/G]TCAGAATTTAAATGA | 25831 |
rs557161358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160126 | ATGTACTTTAAAAAC[A/G]TAATTCATTTAACCC | 25831 |
rs557181893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169113 | TATTCTTTATCTGAC[A/T]TTCCCATATTCCTTG | 25831 |
rs557257693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124850 | TCTCGCTCTGTCACC[C/T]AGGCTGGAGTGCAAT | 25831 |
rs557279138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126208 | AGGATATAATCCTTT[C/T]ATGTTAAAAAAACAA | 25831 |
rs557284597 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182347 | GGTGTATGCCAACAC[A/G]CCGAGCTAGTTTTTA | 25831 |
rs557287644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166496 | GAGTTTTTGTTAAAG[C/G]CAATTAGAAGCTATG | 25831 |
rs557333290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204305 | ATTTCTAGTTCTAGA[G/T]CCTTGAGGAATCGCC | 25831 |
rs557388730 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175068 | CTGTCACGAATGAAG[A/G]TAAGCACACAATTCA | 25831 |
rs557426195 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113044 | AAAAGAAAGTAAAGG[A/G]AATATTAGGAAAAGT | 25831 |
rs557426597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104984 | CCACACCCGCACACC[C/G]GACCACCATCAATTC | 25831 |
rs557508787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202996 | CGGGAGGCTGAAGCA[A/G]GAGAATCACTTGAAC | 25831 |
rs557554161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125250 | CACAATCGTGGCTCA[A/G]TGCAACCTCCGCCTC | 25831 |
rs557555662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147418 | CATTCAAACAGGAAA[C/T]AAAGATGTGAACATC | 25831 |
rs557559063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104126 | TAATGTTTTCTAGCA[C/T]AGTAGGGTGACTATA | 25831 |
rs557573650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203680 | CTGTTATGTTAGGAT[A/G]GAAGGATTTTACATA | 25831 |
rs557602120 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209669 | CTTTGGGAGGCAGAG[A/G]CAGGGGGATCACTTG | 25831 |
rs557648671 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190134 | CCAGGCTCGACCACA[A/T]GCAACAGAACAAATC | 25831 |
rs557708935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196117 | CTCCCGAGTTCAAGC[A/G]ATTCTCGTGCCTCAG | 25831 |
rs557719364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111582 | TATTATGCATGAATT[C/T]ACAGAGAAGAGGTTC | 25831 |
rs557761812 | in-del | -/TATT | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136309 | TTAATATGAATTATC[-/TATT]TAACATTAATTTATT | 25831 |
rs557790528 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196749 | ACAGAGCAAGACTCC[A/G]TCTCAAAACAAAAAA | 25831 |
rs557816198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183189 | AAAAAATAAATTATA[C/T]AGAATTTGTTATATT | 25831 |
rs557844166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197835 | ACCACCACTCCACTC[A/G]GCTCTCATTAAGATC | 25831 |
rs557867979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155902 | TGGTGAAATATTTAG[A/G]TTAAAAGGTAAAACT | 25831 |
rs557923614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111958 | TGCACTCCTGCCTGG[A/G]CGACAGAGCGAGACT | 25831 |
rs557936353 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194263 | GGGTTTGAGTTCAAA[-/G]GGACAGCACTAGATG | 25831 |
rs557936387 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180730 | GATTACAGGCATGAG[C/T]CACTCCACCCAGCCA | 25831 |
rs558072816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125266 | TGCAACCTCCGCCTC[C/T]CAGGTTCAAAAGATT | 25831 |
rs558136653 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207642 | CGGCTCCTCAGGCCC[G/T]GCAACTCAGAGGCCC | 25831 |
rs558169501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168695 | TTGGATACTCCACTT[C/T]GTTCCAAAAATTATT | 25831 |
rs558211033 | snp | C/T | 0.00013796 | 0.00830426 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106304 | GATAAAGCTGACATA[C/T]CAACCAATTTTTGAG | 25831 |
rs558240620 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158970 | AACAAACAAAAAAAA[G/T]GCTTGTCTATTATGT | 25831 |
rs558294786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169200 | AAATTAAGCTGTTAA[A/G]CAGGTTTATTAAATA | 25831 |
rs558309918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129594 | CTGCCCACTAAAATA[C/T]ATGTAAATTTTTGGA | 25831 |
rs558322467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115644 | GCACACCTGTAGTCC[C/T]AGCTACTCAGGGGAC | 25831 |
rs558348187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119284 | GGAGAAATTAGTATG[A/C]CTACCACAATCTAAA | 25831 |
rs558478236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175796 | TTGAACCTGGGAGGC[A/G]GAGGTTGTCGTGAGC | 25831 |
rs558480229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31184415 | GGACAACAAAGTGAG[A/G]CCCTGTCACTACAAA | 25831 |
rs558508149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172346 | CCGTGGCTCACGCCT[A/G]TAATCCCAGCACTCT | 25831 |
rs558514626 | snp | C/T | 1.65663e-05 | 0.002878 | missense | HECTD1 | GRCh38.p7 | 14:31116360 | TGAGTGGTAATTCAA[C/T]TTCACGAGTCGTTCC | 25831 |
rs558532240 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209045 | CGCAGGTAATGGTCC[A/G]TTTAGGTATCCTGTT | 25831 |
rs558549513 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147128 | ACTATCCTGGCTAAC[A/G]CAGTGAAACCCTGTC | 25831 |
rs558567975 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208177 | ATCTTCCCTCCTCGC[G/T]CACGGAAGTGCGTCG | 25831 |
rs558574300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109784 | AAAATATATGAAACT[C/T]CTTTTATTATAATCT | 25831 |
rs558586391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182105 | CACCATGTTGGCCAG[C/G]CTGATCTAGAACTTC | 25831 |
rs558611858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102575 | GCTGGGATTACAGGC[A/G]TCTGCCACCACGCCC | 25831 |
rs558612015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110542 | AAATGGCATTAAATG[A/G]TACAAAAATGTAACT | 25831 |
rs558629442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166201 | ATATAAAAAGTGTAA[C/T]GGGGTAAATTTAAAT | 25831 |
rs558681637 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187449 | ATAACCTCTTATACA[A/T]CTACATAAGAGCTAT | 25831 |
rs558694635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117140 | AACACTTTGGGAGGC[C/T]GAGGCGGGTAGATCA | 25831 |
rs558772805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188750 | GACACTAGCCTTTTA[C/T]ATGCTGAATAACTTT | 25831 |
rs558806916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174177 | AAATAACATCTGAAC[A/G]ATAAAAAGTCATTAA | 25831 |
rs558816998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185215 | GGTGTGGTGGCAGGC[A/G]CCTGTAGTTCCAGCT | 25831 |
rs558835621 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171527 | GTTCAACACTAGGTG[A/C]CTAGTTGAATAAACT | 25831 |
rs558850716 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179376 | GTGAGCTGATATTGC[A/G]CCACTGCACTCCAGC | 25831 |
rs558881026 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149292 | AAACTGGAAATATTA[A/G]CCAGGCATGGTGGTA | 25831 |
rs558898922 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155211 | TTAGCTGGGCGTGGT[A/G]GTACGTGCCTGTAAT | 25831 |
rs558914580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180124 | TGGAGGTTGCAGTGA[A/G]CTGAGATCATGCCAC | 25831 |
rs558944357 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153047 | AAAATCTGAGAGAAT[G/T]ATCTGGCTTGCCTTT | 25831 |
rs559019970 | snp | C/T | 0.000239794 | 0.0109471 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144046 | TAAAAACCACTCTAC[C/T]GAAGGAGTAACTACA | 25831 |
rs559058306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145080 | GCACAAATGAGCTCT[C/T]GAAGTTACAGTTATT | 25831 |
rs559060274 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137714 | CACTGCACTCCAGCC[C/T]GTGCAACAGAGCTAG | 25831 |
rs559117356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115685 | AAATCACCTGAGCCT[G/T]TGGAGTTTGAGGCTG | 25831 |
rs559136719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131526 | TGTACTTCAATAAAA[A/T]GCTTATGTATGTATA | 25831 |
rs559190141 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143420 | TCTGTGTCAAAAATA[-/T]AATAAATATATAAAC | 25831 |
rs559257783 | snp | C/T | 3.31246e-05 | 0.00406955 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31102963 | GTAATTGATAATATC[C/T]TCTGCTGCCCAGGAT | 25831 |
rs559266947 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146035 | CAATGTCCTCACTGA[-/T]TTTTTTTTAGTTTGT | 25831 |
rs559313340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138352 | TTTCTGTATAAATCT[G/T]AACTAATTCCTATAA | 25831 |
rs559321985 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202381 | ACCCAAGTCTATCCC[A/C]TTGCAGAGGCCACTG | 25831 |
rs559332290 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195694 | CCTCTGCTAATTTTT[C/G]TATTTTTAGTAGAGA | 25831 |
rs559334496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203154 | TAAGGCTCTCAGAGG[A/C]TAATGAACACAACAG | 25831 |
rs559339479 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188262 | TTTTTTTGAGACAGA[A/G]TCTTGCTCTGTCGCC | 25831 |
rs559343305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115235 | CTTGGGGAAAAAAAA[C/T]TGAAGGGCGGGAGAA | 25831 |
rs559379778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165394 | TCTCAATCAACACTT[C/G]TCTGTTTCTATTCTC | 25831 |
rs559412434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167328 | CTGGTCATGGTGGCA[A/T]ACTTGTAGTCTCAGC | 25831 |
rs559454720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194013 | GTTTATAGCAGTTTA[A/G]GTCATAATCACCAAA | 25831 |
rs559465073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159058 | GGCACTAAGCTGCAG[A/G]TATCATTACCCTTGA | 25831 |
rs559487581 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207724 | ATCGCGAACCGGGAG[G/T]GGGAGGGGAGGAGGG | 25831 |
rs559510098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193267 | TAGTGTGAGATAGTA[C/T]CAAAGTTAAACTTAC | 25831 |
rs559516475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109950 | AGAAATGATTAAGCT[A/G]TCTTTCAAACTGAAA | 25831 |
rs559519366 | in-del | -/TTCT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188540 | CGCCCGGCCTTGTTA[-/TTCT]TTCTATCTCAGCCTA | 25831 |
rs559546658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111291 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 25831 |
rs559551582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166856 | ACTTTGTCTCTAAAA[A/C]AAATTTTTAAAAAAA | 25831 |
rs559551590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174364 | AGCCTGGCCAATATG[A/G]TGAAACCCTGTCTCT | 25831 |
rs559636254 | snp | A/G | 0.000116882 | 0.00764378 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173652 | CGACCTGGTTTGCAT[A/G]CTGATGATGGTCCTG | 25831 |
rs559693519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111636 | TGGTTTTCACACAGC[A/G]CGCTTCTCTGGGTGG | 25831 |
rs559721140 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207247 | AAAGGGGCCAGCGGG[A/G]AAGTCGGCAGCAGCC | 25831 |
rs559779996 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116058 | AGACTGTAAATGTCC[G/T]TCTACTTCTAAAACT | 25831 |
rs559801014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160321 | ATTTTCCTGTTTAAC[A/G]CTATTATATAAATTT | 25831 |
rs559834090 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209190 | AAGTGGCATTCCCTC[A/T]GGACCTTGAAGAATG | 25831 |
rs559844017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117229 | AATGCAAAAATTAGC[G/T]GGACATGATGATGCC | 25831 |
rs559905889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153245 | AAAATACAAAAAATT[A/T]GCCGGGCATTGTGGC | 25831 |
rs559907051 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132263 | ACCAACATGGAGAAA[C/T]CCCGTCTCTACTAAA | 25831 |
rs559911428 | snp | A/C | 0.000656134 | 0.0181007 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106606 | AAAGCTTTAAAACTT[A/C]TTCATGCATTGGATT | 25831 |
rs559951012 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181483 | AAGCCAGGCTGGTAG[G/T]GTGCACCTGTGGTCC | 25831 |
rs559994565 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163880 | ATCACGCCACTTCAC[C/T]GCAGCCTGGGTGACA | 25831 |
rs560029724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176854 | AGGCAGGAGAACCGC[C/T]TGAACCCAGGAGGCA | 25831 |
rs560041605 | snp | A/C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120675 | CATGTAAGTACACAC[A/C/G]TGCACATCCACAGTT | 25831 |
rs560043599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130850 | CTATTTTTTTCTGTA[C/T]GCTGAAATAATCTCT | 25831 |
rs560064239 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160435 | AGAGGGATTCTTGGA[C/T]CTAACAGCCTAAACA | 25831 |
rs560075643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106034 | TATGACAGCAACATG[C/T]TTGTAAGACTTTTAG | 25831 |
rs560135759 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121951 | ACTCTTCCACTTAAC[G/T]CTGATGATAAGGGCA | 25831 |
rs560155450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156621 | TAGTGAATTTGGATA[A/G]AGAGTATTCTGATAT | 25831 |
rs560182314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163395 | CTGCAGTGAGCCAAG[A/G]TTGTGCCACTGCACT | 25831 |
rs560235027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113573 | ACTATGAAAGGGTTG[G/T]AATTTTTTAAAGTGC | 25831 |
rs560252275 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197711 | ATCTCTTTGACCTTT[A/G]AAAGAAAAAACCCCA | 25831 |
rs560262326 | snp | C/G | 1.65652e-05 | 0.0028779 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127928 | CTGCTAGTAACACTG[C/G]ATGTTGACATAGTCA | 25831 |
rs560292855 | snp | A/G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126172 | TTTCACAATGTATTG[A/G/T]GTGAAAACAGCTGGC | 25831 |
rs560305919 | snp | G/T | 1.65685e-05 | 0.00287819 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101101 | CACAACAGAAGACCA[G/T]GAGTTTAAATACTTC | 25831 |
rs560322558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169526 | TTTCTTTGACATCCA[A/G]CTATGTAAACTAAAG | 25831 |
rs560329490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120159 | GGAGGCTGAGGCAGG[C/T]GAATCACAAGGTCAG | 25831 |
rs560377750 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199456 | TGGAGTGCAGTGGGG[C/T]GATCTCGGCTCACTG | 25831 |
rs560387346 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131540 | ATGCTTATGTATGTA[C/T]AGGAATGTCACAGTG | 25831 |
rs560392809 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119616 | AAAACTAAAAAAAAA[A/T]TTTTAATAACGTGCA | 25831 |
rs560427734 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108036 | TTGCTTGAAGAAATG[A/G]TGGTGAACAGACTTT | 25831 |
rs560456848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143184 | CTTGGGAGGCAAAGG[C/T]GGGCGGGTCACTTGA | 25831 |
rs560501927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171686 | ATATATATATTTGTT[G/T]TTATTGAATCTGTAT | 25831 |
rs560529880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136427 | AATTACTGGGCCAAA[C/G]TGTATTACCATAACT | 25831 |
rs560556260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114757 | TTAAAGATATGACTG[C/T]ATCAAGTGTTATGCA | 25831 |
rs560560941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186225 | AATATCACTATCTCC[A/G]TTTAGAAATATCACA | 25831 |
rs560604338 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149475 | AAAGGAGCTATATTT[A/G]TAAAGATATTTTTTA | 25831 |
rs560644748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164595 | TCCTCACCTTGGAGA[C/T]GAGCCAATTGATTAA | 25831 |
rs560677001 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150720 | TACATCTCTGGGCCT[A/C]TTTGTAAACAATGAT | 25831 |
rs560719823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107947 | TACATTTACTTCTCA[C/T]AACAACCCTGCAAAA | 25831 |
rs560734208 | in-del | -/TT | 0.00676609 | 0.0577691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108534 | TCTATATTAGAAGAA[-/TT]TGTAAACAACTGGGC | 25831 |
rs560764260 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206712 | GTAGGCCAACCTAGG[A/G/T]CCCTCTTTCCCCAGC | 25831 |
rs560766136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149932 | CCTTGACAATGGTAG[C/G]AAAAATATGAGAAAA | 25831 |
rs560779273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164048 | AAATTCTATGTAGCT[C/T]TCTTCTAAAACAAAG | 25831 |
rs560802446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150489 | CCTCAACCTCCCAAG[C/T]AGCTGGGATTACAGG | 25831 |
rs560827396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157675 | AGTGCAGCGGCTCAC[A/G]CGTGTAATCCCTGCA | 25831 |
rs560875602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142386 | GAGAATAAATGCAAA[C/T]AGTAAAGTTTATGAA | 25831 |
rs560933142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115269 | CGTTATGATTTTCTG[C/T]TCTATTTCAAAAGGA | 25831 |
rs560984237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177628 | AATGTCTAGCACTGG[C/T]GGGTGGTGTTTGTTG | 25831 |
rs561031656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154221 | CTGCAACCTCTGCCT[C/T]CCAGGTTCAAGCAAT | 25831 |
rs561033014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156752 | TATTGTCATTATCCT[A/G]TCAAAAACCATCAAA | 25831 |
rs561049560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120281 | CCCAGCTACTCGGGA[A/G]GCTGAGGCAGGAGAA | 25831 |
rs561072980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126946 | AAAGTGCTGGGATTA[C/T]AGGCGCAAGCCACCA | 25831 |
rs561073220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185597 | GCAGGTGTGGGGACA[C/T]GTGCCTGAGGTCCCA | 25831 |
rs561090750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114122 | ATGATATTTCACATG[C/T]ATTACATGAGGTAGC | 25831 |
rs561090761 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121031 | TAGTGATCATTAAGC[A/G]TTAGCTATTAATAAA | 25831 |
rs561146709 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207830 | CGGCGACCCCGCCGG[C/T]GGCCACCTGGGGCGC | 25831 |
rs561219666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193107 | AATTTATTCTCTTAT[C/G]AATTGTGCTTTTGGT | 25831 |
rs561271690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122143 | AAGTTCATACACTGT[G/T]TGTGTGCTTGGGTGT | 25831 |
rs561301070 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165915 | CAGTGGCGCAATCTT[A/G]GCTCACTGCAACCTC | 25831 |
rs561333647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118163 | GGCGCGCACCACCAA[A/G]CCTGGCTAATTTTTG | 25831 |
rs561389050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165461 | AGTGATCTTGATCAA[C/T]AGAAATCCAGATGTG | 25831 |
rs561391484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180527 | TTGGCTCACTGCAGC[C/T]TCTGTCTCCCATGTT | 25831 |
rs561407095 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117590 | CTTCATTATCATGAT[C/T]GTCTTCTAAAATATT | 25831 |
rs561419743 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179176 | GTAATCCTTGCACTT[C/T]GGGAGGCCGAGGCAG | 25831 |
rs561429269 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145447 | GCAGGCAGATCACTT[C/G]AGGTCAGTCAGGAGT | 25831 |
rs561452917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172448 | TAAAAACACAAAAAT[C/T]AGGCGGGTGTGGTGG | 25831 |
rs561489663 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108485 | TTGCATAAAGTATAA[C/T]AAAAACTACAGCATA | 25831 |
rs561490950 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181830 | CAAGGTATCCGGGGC[A/G]TATTCCTACATACGT | 25831 |
rs561582199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183625 | TCAGTGGAGGGCCTT[C/T]TAAGTCAAAAACTAT | 25831 |
rs561593498 | in-del | -/GA | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153791 | TGGGTAGTAAGGGTT[-/GA]GACTAAGGGAGACTC | 25831 |
rs561596936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186310 | CCAAATCTCCATCAT[A/G]GTAAATGTCAACCAT | 25831 |
rs561653330 | in-del | -/CTT | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198494 | CCATGAGCTTGAAAG[-/CTT]CTGAATATTTAAAAA | 25831 |
rs561682231 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132991 | TAGGGGAAAAAACCG[C/G]AAGTGTGTCTTGAAG | 25831 |
rs561695474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168758 | AAACTTAAAACTTTG[A/G]TCAGCCGGGAGCAGT | 25831 |
rs561771851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135670 | TGCTGTTTTCAAGCA[C/T]GTTACCTACTTTTTT | 25831 |
rs561803578 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104279 | CTGTGTATCAAAATG[C/T]CCCATAAACATGTAC | 25831 |
rs561830399 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154345 | CTCTGTCGCCCAGGC[C/T]GGAGTACAGTGGCGC | 25831 |
rs561835284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140075 | AATATGGTAATCAAC[C/T]TCAATATATACCCCT | 25831 |
rs561841829 | snp | G/T | 5.00396e-05 | 0.00500173 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168478 | ATCCAATCACCTACA[G/T]ACAAATATTTTTTAA | 25831 |
rs561870697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125013 | AGGTTTCGCCATATT[A/G]GCCAGGCTAGTCTCG | 25831 |
rs561879025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141385 | TATTATCAAACATTT[C/T]ATCAGTGTTCAAATT | 25831 |
rs561888096 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162869 | GCTTAAGAGTTCAAG[-/A]CCAGTCTGGGCAACA | 25831 |
rs561903597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148366 | ACAAGGTATTAACCC[A/G]GATTGTAAAATACAA | 25831 |
rs561906667 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189654 | ATAGTCCCAGCTACC[G/T]GATGGGGGTTAGAGG | 25831 |
rs561960343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146840 | CATAGGAAACAGAGT[A/G]AGACTCTGTCTCAAA | 25831 |
rs561961788 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156401 | AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 25831 |
rs561964396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182822 | AGACACTGCACTCCA[A/G]CCTGGGCAATAGAGT | 25831 |
rs562002526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112679 | CAGTGGTACGATCTC[A/G]GCTCACTGCAGCCTC | 25831 |
rs562015546 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191771 | TGGGAGGTCGAGGCA[G/T]GCGGATCACCTGAGG | 25831 |
rs562022969 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170070 | GGCAATCAATGACAT[C/T]GCCTCCTATATACTG | 25831 |
rs562036473 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202009 | AGTGGAGAGCCGGCC[A/G]GGCGCGGTGGCTCAC | 25831 |
rs562050143 | in-del | -/A | 0.235273 | 0.249566 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156246 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAGCT | 25831 |
rs562084858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134402 | CCTTAATTCTATAAC[A/G]AGCAATAGCCACTGC | 25831 |
rs562100758 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185064 | ACTGATGCTTCTGGC[C/T]GGGCGCGGTGGCTCA | 25831 |
rs562138439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191316 | AGATGGCTTTAGCTC[A/G]GGAGTTCCAGACCAG | 25831 |
rs562140856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204577 | AGGTTACCTCTAATG[A/C]AATCTATGAACGCAA | 25831 |
rs562157632 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176938 | CAAGACTATCTCTCA[A/G]AAAAAAAAAAAAAAA | 25831 |
rs562158110 | snp | A/G | 0.000182747 | 0.0095572 | missense | HECTD1 | GRCh38.p7 | 14:31113465 | TTTAACCCAGACTTT[A/G]TTCCATGCTCACAAA | 25831 |
rs562167328 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31123164 | GGGACAACTGTTGCG[C/T]TCTGCCACCACATAC | 25831 |
rs562200304 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206060 | TAGAACCAAATTTTC[-/AT]AGTGTCCTCCTAGCA | 25831 |
rs562264569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197233 | CTCAGGGCCAGGCAC[C/T]GTGGCTGGTCTCGAA | 25831 |
rs562276894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197915 | CCCTACTTGACCTCT[C/T]ACTAGTATTCAAAAC | 25831 |
rs562289305 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124522 | GCTTTAAGAATATAA[A/C]AAAGAAAATCTTCTA | 25831 |
rs562339894 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197959 | CTTCTTGAATCACTT[C/T]CTTTCCTGTGTTGAC | 25831 |
rs562352728 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179674 | TATTTTATCAACACT[C/T]AAAATATGAAAAGAT | 25831 |
rs562399188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31162168 | ACCTGGGAGTCAGAG[A/G]TTTGCAGTGAGCCAA | 25831 |
rs562405847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176808 | CGCGCATGGTGGCAC[C/G]CGCCTGTAGTCCCAC | 25831 |
rs562413357 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182875 | TAATTAAAAAAAAAA[A/C]AACTCACATTACTAT | 25831 |
rs562413417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190311 | TCTTGTTTAATACTA[C/T]TAACTTTGGGGTGAT | 25831 |
rs562440188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204001 | AGAACATGCATTTGG[C/T]GTTTTGTCCTTGCGA | 25831 |
rs562502244 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163195 | TGGGAGGCTGACGTC[A/G]GAAGATCGCTTGAGC | 25831 |
rs562505271 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126980 | CTGACCAGATTTTTT[C/T]TTTTTTTTTGAGACG | 25831 |
rs562511580 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136034 | AACAAAACAACAACA[A/T]CAACAAAAACAAAAA | 25831 |
rs562554312 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167665 | ACTGTAGAGGGAGAG[C/G]CACAAGGAGTTCCTG | 25831 |
rs562563762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168896 | AAATACAAAAAAAAT[C/T]AGCTGGGCACGGTGG | 25831 |
rs562631849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148129 | ATGAGATTATCTTAC[C/T]TTTTTTTAAAAATGA | 25831 |
rs562640621 | snp | G/T | 1.7957e-05 | 0.00299636 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133207 | ATTTAACTACCCATT[G/T]TCTACACAAAAGTGC | 25831 |
rs562641153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118807 | GCGGAGGCAGGAGAA[C/T]TGTTTGAACCTGGGA | 25831 |
rs562687721 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131288 | CTAAAACGAACAAAC[-/A]AACAAAAAACACTCA | 25831 |
rs562704524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125451 | GAGCTAGGATTACAG[A/G]CGTGAGCCACAGCGC | 25831 |
rs562731493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106564 | CTATTTACTCATATA[C/T]TGCAAATCAGTGACG | 25831 |
rs562764725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140220 | TTAATTATATTTAAA[A/G]CAGATGTATGATTTA | 25831 |
rs562794283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105963 | GAAACCACCTTTCTA[C/T]ATTTTACTTCTAACT | 25831 |
rs562801282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140750 | TTATACATCCATAAA[A/G]ATATAATATGCATTC | 25831 |
rs562802851 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132477 | ATATACACACACATA[C/T]ATGTGGATATATATA | 25831 |
rs562834741 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175251 | AACAGAAAAGTGAAA[A/C]AAATGAAATTAATTT | 25831 |
rs562853794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186077 | TTCCTAGATTCCCTC[A/G]TCATCTTTCCTATCT | 25831 |
rs562872606 | in-del | -/A | 0.067446 | 0.170804 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185725 | AGTGAGACCCTGTTT[-/A]AAAAAAAAAAAGAAG | 25831 |
rs562892736 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152679 | CTAGCCTTGGCAACA[C/T]TGTGAGACCCGCATC | 25831 |
rs562893079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149785 | ACAGGTGCCTGTAGT[C/G]CCAGCTACTCAGGAG | 25831 |
rs562911008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139087 | GAGGAGGGAAGGAAA[A/C]GAGGCTATGAAACCA | 25831 |
rs562919827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198617 | CTCAGTGGACTGATA[C/T]TTTCCACATGACCAA | 25831 |
rs562924526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185537 | GTTCGAGACCATCCT[A/G]GGCAACATGGTAAAA | 25831 |
rs562943621 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177146 | CAAGTCTTGACTCTT[-/C]TGCTCACTACTCCCA | 25831 |
rs562947930 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131684 | CCTATGCAATTGCTT[C/T]AGTTGACTCCATCCT | 25831 |
rs562948845 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170079 | TGACATCGCCTCCTA[G/T]ATACTGCCAATTACC | 25831 |
rs562966363 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31100115 | CACATGACACAGTTC[C/T]GTACGCTGCAAACAT | 25831 |
rs562968048 | snp | C/T | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121347 | TAAAAGGGAAAAATA[C/T]ACATATGGTAGGGAA | 25831 |
rs563015434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177763 | AACATAGCAATCACC[C/T]ACAGTTTTCCTTCTA | 25831 |
rs563040085 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202925 | GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT | 25831 |
rs563051381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191410 | ACATGCCTGTAATCC[C/T]AGCTAGTCAGGAGGC | 25831 |
rs563081385 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200783 | AAGACTCTTGTCTTG[-/A]AAAAAAAAAAAAGAA | 25831 |
rs563097287 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145214 | CATTTTAATCCCAAA[A/C]AAACCCAGCATAACT | 25831 |
rs563104674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131124 | TCTCTGACATAGAGA[C/T]TCAAAGGCATAACTT | 25831 |
rs563106958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206593 | TGGTTAGGAATTTTG[C/G]CAGTCTTGGCAACTA | 25831 |
rs563128461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170804 | TACAGTAAATCTATA[C/T]AATATATTTTTCTAA | 25831 |
rs563165359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198003 | ATGCAAAAGCAATAG[C/T]GGATAAAACTGCAGG | 25831 |
rs563173082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156019 | CTGGGAGGCAGAGGC[A/G]GGCGGATCACGAGGT | 25831 |
rs563186470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173866 | AGGGTTAGTAATGAT[C/G]ATTTCAATACTGACA | 25831 |
rs563204554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110103 | CTATCCCGGGTTCAA[G/T]TGATTCTCCTGCCTC | 25831 |
rs563336649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102673 | GACCTCAAGTGATCC[A/G]CCCGCCTTAGCCTCC | 25831 |
rs563345287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182211 | TTTTTTTTTTTTCCA[G/T]ACAGGGTCTTGCTCT | 25831 |
rs563349941 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195342 | GGGACACAAAGATGA[A/G]TAAGAAAGAGTTCAC | 25831 |
rs563350318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31189864 | TTAAAATGTGACTTT[C/G]ATAGTCTTCCCTATG | 25831 |
rs563365370 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185509 | GATGTGGGCAGGTCA[C/T]TTGAGCCCAGGAGTT | 25831 |
rs563392452 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188126 | AGATAGATAGATAGA[C/T]AGATAGATAGATAGA | 25831 |
rs563431612 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159091 | TGAATGATAGAAGGA[A/T]AAAGAGGCAAAATTT | 25831 |
rs563451786 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153118 | GATGGGTCGGCCAGG[C/T]GTGGTGGCTCATGCC | 25831 |
rs563466520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200724 | AGGTGGAGGTTGCAG[C/T]GAGCTCAGATCACGC | 25831 |
rs563494534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201551 | GTCTCACTCTGTCAC[C/T]GAGGCTGGAGTGCAA | 25831 |
rs563533050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103280 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 25831 |
rs563539516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196992 | CTCCTTCAGTATCTG[C/G]ATATTAGCTATTTGT | 25831 |
rs563572780 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168009 | ATACCGTCCCTACCA[A/C]CAGGCTTCTAAAAAG | 25831 |
rs563574825 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160456 | AGCCTAAACACTTTC[A/C]TTAAGTATTGAATGT | 25831 |
rs563582521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103860 | TAATCCCAGCTACTC[A/G]GGAGGCTGAAGCAGG | 25831 |
rs563609082 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153917 | GTTCATTTTTTGAAA[A/T]GATCATCCTTTCTTG | 25831 |
rs563624311 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31123985 | TAATGCTTTGAAATC[A/G]GAATGTATCTTACAA | 25831 |
rs563655285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147705 | AGAGGTTACAGTGAG[C/T]TGAGACTGCACCATT | 25831 |
rs563662455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167433 | CAGCCCAGGTGACAG[C/T]GATACCCTGTCTCAA | 25831 |
rs563705498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124118 | GTTACCCTTTAACAC[C/T]TGTAAGGAGCCACCT | 25831 |
rs563733716 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112068 | TTCCAGTTTAGCCAC[A/G]GTAACACTTGTGGGG | 25831 |
rs563744175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124961 | TACAGGGATCCGCCA[A/C]CACACCCGGTTAGTT | 25831 |
rs563820988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154468 | ATGCCTGGCTCATTT[C/T]TGTATTTTTTGTAGA | 25831 |
rs563866012 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209268 | ATGTTCCTAGACATA[G/T]GAAAGGTCACCTGTG | 25831 |
rs563866254 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131877 | ACTATTCAACTCAGT[A/G]TAACAATAATAGTTG | 25831 |
rs563890569 | snp | G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31210023 | CAAGTTTTTTGTTGT[G/T]TTTTTTTTTTTTTTT | 25831 |
rs563929755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117411 | AGAAAACTAAAAGTA[C/T]CCATACTCAGAGAAA | 25831 |
rs563930200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103717 | TCACACCTGTAATCT[C/T]AGCACTTTGGGAGGC | 25831 |
rs563992218 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103367 | CTAACACAGTGAAAC[C/T]CCGTCTCTACTAAAT | 25831 |
rs564017621 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31121958 | CACTTAACTCTGATG[A/C]TAAGGGCAAATTTTT | 25831 |
rs564065440 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124348 | GATTTGACCACATCA[C/T]AGAATAAAATGTCTC | 25831 |
rs564072715 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31170970 | CTCGTACTATACCAA[A/G]TAACTTCACGATTGG | 25831 |
rs564078895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138470 | TCTTGCACAATCTCC[A/T]GAAGTGAAAAATGCA | 25831 |
rs564098621 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163719 | GTTTAAGGCCAGGCT[C/G]GCCAACATGGCAAAA | 25831 |
rs564104520 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197867 | ATGACCTTGAGAATG[C/T]TGCTAAATCTAAAGG | 25831 |
rs564121481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182300 | GGCTCAACCTTCCTC[C/T]CACCTCAGCCTCCCA | 25831 |
rs564178167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183886 | TTAATTTTTTTATTT[C/T]TGGTAGAGACAAGTT | 25831 |
rs564201182 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159632 | GCGTGAGCCACCGCA[C/T]CTGGCCATAATTTTT | 25831 |
rs564218343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155255 | GAGGCTGAGGCATGA[A/G]AGTCGCTTTAACCCA | 25831 |
rs564287387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195511 | CTGTTGAAACTATTA[A/G]GAGTGGTTTTTAACT | 25831 |
rs564298946 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191060 | TTTCAGGAGCTCCAA[A/T]CTCCTGGGCTCAAGC | 25831 |
rs564301369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154549 | GTGATCTCCCTGCCT[C/T]GGCCTCCCAAAGTGC | 25831 |
rs564334831 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141323 | AAAAGAATTATTTTT[A/T]AAAAAAAAACAGTAT | 25831 |
rs564349068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188901 | CTGGCCCAATTCCCA[C/T]AGGGTCACCCACCTC | 25831 |
rs564361704 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191214 | AAATACTATCCCATA[A/T]TTTGCTTATTTCCTT | 25831 |
rs564364695 | in-del | -/TT | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130347 | GAGCATACTGAACTC[-/TT]TTATTAGAACTATCT | 25831 |
rs564478228 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117091 | TTTAATTTTATAAAT[A/G]AGGCCAGGAGCAGTG | 25831 |
rs564484527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161973 | AGGGGCTCACACCTG[C/T]AATTCCAACACTTTG | 25831 |
rs564527065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105038 | CAGCGGAGTTTTGCT[C/T]ATCGCCCAGGCTGGA | 25831 |
rs564527650 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196551 | CGAGGTCAGGAGTTC[C/G]AGACCAGCCTGGCCT | 25831 |
rs564540687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112612 | TGCATTCATTCATTC[A/G]TTCATTTTTTTTTTT | 25831 |
rs564568716 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197046 | TGGGAAAACAAAGAC[A/C/G]AGCTCGTAGTCCAGT | 25831 |
rs564580026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187206 | ACACAAAAAATCAAA[C/T]TAGCAAGGGGCAGTG | 25831 |
rs564670954 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203898 | TGCTATCCCTCCCCC[C/G]TCCCCCTACCCCACA | 25831 |
rs564677765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143903 | AGCAAATTATAACTG[A/G]GAACTTAGAAATCAA | 25831 |
rs564686933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104609 | ATACTTTGTTCCCAT[C/T]ATGATTCTTTCATGT | 25831 |
rs564710416 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191525 | AGATGGGGTTTCTCC[A/G]TATGGACCAGACCCT | 25831 |
rs564774264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165264 | CAAAAACCTGCAGTC[A/C]TCTTTCACCCTTTCT | 25831 |
rs564791938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168126 | CTAAAACTTCTCTTC[A/G]TTCAGATCGTCAGAA | 25831 |
rs564815113 | snp | A/G | 3.33056e-05 | 0.00408065 | missense | HECTD1 | GRCh38.p7 | 14:31106862 | CCATTAAACCAAGCT[A/G]GGGGTTTTGGTTTAG | 25831 |
rs564842086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151745 | GTAGCTCAGCCTGTG[C/T]TCCTAAAACTTTTTT | 25831 |
rs564859858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164623 | TAAGAGGTTATGTGC[C/T]TTGCCCATGGCCAAA | 25831 |
rs564862287 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180005 | ACATGATGAAATCCC[C/G]TCTCTACTAAAAATA | 25831 |
rs564863117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101822 | AAATCCCTCAAAGAC[C/T]GTCTTGAACTTACAA | 25831 |
rs564916170 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110174 | GCCCAGCTAATTTTT[C/G]TATTTTTAGTAGAGA | 25831 |
rs564925827 | snp | A/G | 1.7056e-05 | 0.00292022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101353 | AATATAGTTATATTG[A/G]GTTGACTGCAGATTT | 25831 |
rs564925957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108686 | AAAAAAGAAGAAGAA[C/G]AACATAAGGGTAGGA | 25831 |
rs564928141 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208480 | GCATTCAGAATAAAG[A/G]ATGCATGCTTATAGG | 25831 |
rs564935721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193880 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 25831 |
rs564938678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201644 | CCTCCCAAGTAGCTG[A/G]GATTACAGGCACATG | 25831 |
rs564969316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150967 | TGAGGGTGGTAGTGC[A/G]CACCTGTAGTCCTAG | 25831 |
rs565064414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206645 | AAAAAATTAAAAAAG[G/T]AAAGGCTAAAAGTAA | 25831 |
rs565065415 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207973 | CGGCTTTTCTATGGT[A/G]CGCCCTGGCCCCCTT | 25831 |
rs565092547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31199809 | AACAAAAGTTCTTCA[C/G]GATCCACAATAATTT | 25831 |
rs565321215 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171246 | GCAAAACCCTGTCTC[G/T]ACTATAAGTACAAAA | 25831 |
rs565365879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172535 | CAGGAGGCAGAGGAC[A/G]CAGTGAGCCAAGATT | 25831 |
rs565368987 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173401 | GCACTTTCAATTGAA[C/T]CTGGAAGCTCCGACC | 25831 |
rs565379330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159272 | AAAATGATAGGTGGA[C/G]AGAGGACAAACTGTT | 25831 |
rs565407705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179212 | TCACTTGAGGTCAGG[A/T]GTTCAAGAACAGACT | 25831 |
rs565429894 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155740 | ATTTCATTGTGGACC[-/A]GAAAAAAAAATTACT | 25831 |
rs565435004 | snp | C/T | 0.000172113 | 0.00927508 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113215 | AATTAATAAAATTAA[C/T]AAAAATATAAACTGA | 25831 |
rs565443200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130033 | GGTAAAATACTGCCA[C/G]TTCAGCAAGTAAACA | 25831 |
rs565488421 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115692 | CTGAGCCTGTGGAGT[C/T]TGAGGCTGCAGTGAG | 25831 |
rs565494817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196526 | TTGGGAGGCCGAGGC[A/G]GGAGGATCACGAGGT | 25831 |
rs565563460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145008 | AAATCTTCACTTTTA[C/T]AGACACTCGTATTTA | 25831 |
rs565576125 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180171 | GCAAAACTCCGTCTT[-/A]AAAAAAAAAAATCTG | 25831 |
rs565603745 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137696 | AGCGAGCTGAGATCA[C/G]GACACTGCACTCCAG | 25831 |
rs565621276 | snp | C/T | 0.00013249 | 0.00813802 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150189 | TGGTTTACCTTGTTG[C/T]AATTCTTTAGCATCT | 25831 |
rs565657323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142733 | GGCACGAGCCACCGC[A/G]CCCAGCCTAAAGTAA | 25831 |
rs565668815 | in-del | -/GGAGGCTGAA | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103861 | AATCCCAGCTACTCG[-/GGAGGCTGAA]GCAGGAAAATCGCCT | 25831 |
rs565689106 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31113664 | TTCCCAAATAAAATA[C/T]AACCACTCTAAGCCA | 25831 |
rs565747032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186562 | GCGTGGTGGCACGTG[G/T]CTGTTATCCCAGCTA | 25831 |
rs565754551 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207438 | GCTCCCAACAGGCCG[C/T]CGGCAGAGCCAGGCC | 25831 |
rs565800416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137373 | GACCTCAGGTGACCC[A/G]CCTACCTTGGTCTCC | 25831 |
rs565876553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101444 | CTCACACCAGAACAA[C/G]AACACATCTAGAGAC | 25831 |
rs565893333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138099 | AAATCTGAAACTTTC[C/T]GAGCACTGACATGAT | 25831 |
rs565895329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200575 | ACTTGAGGTCAGGAA[C/T]TCGAGACCAGCCTGG | 25831 |
rs565922397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108158 | GTGCAGTGGCACGAT[C/G]TCAGCTCACTGCAAC | 25831 |
rs565939381 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100539 | GTAGCTTAAAAGCCA[C/G]CAAAACAGGGATCAG | 25831 |
rs565940060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188049 | GCGTGAGTCACCACA[A/C]CTGGCCTGAACACAT | 25831 |
rs565947446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180603 | GCACACGCCACCACA[A/C]ACAGCTAATTTTTGT | 25831 |
rs565948119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181151 | CATCCATTTTTCTTA[C/T]CCAGGGTAAAAACTG | 25831 |
rs565955636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157801 | AACTAGCTAGACGTG[G/T]TGGCAGGCACCTGTA | 25831 |
rs566002720 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192242 | TCCGCTGAGGTAGGA[C/G]GACAATCGCTTGAAC | 25831 |
rs566048596 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186180 | TATCACAAAAACTCC[C/T]TAAGTATTTTCTCCA | 25831 |
rs566076616 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188546 | GCCTTGTTATTCTTT[C/G]TATCTCAGCCTAAAT | 25831 |
rs566115894 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154036 | TTACCAAAGTTTTAT[A/G]AAAGAGTTGAAATTG | 25831 |
rs566120396 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198178 | ACCCCTGAAGATACA[C/T]CTTTTCAATATTCTA | 25831 |
rs566123714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102761 | TTTGTATCCTCCCAG[C/G]CTTATCAGTGGATAT | 25831 |
rs566160790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152713 | ACAAAAATAAAATAA[A/G]TATTTTTTTAATTAA | 25831 |
rs566187287 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185036 | TTGTAATTTAAACAG[A/G]TAAGATTTAAAAACT | 25831 |
rs566187781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105300 | GCCACCGTGCCCAGC[C/T]GACCACCAGCAATTC | 25831 |
rs566197794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145423 | ATCCTAGCACTTTGG[G/T]AGGCCAAGGCAGGCA | 25831 |
rs566200545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165723 | TAAGGATCAGGCCCT[A/C]TTCTGTATCTCCTTG | 25831 |
rs566263023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158588 | CTTTATAACATGTAA[C/T]CTGATCTTTTAAAAT | 25831 |
rs566283502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110343 | CCATTTATGGTGGGA[A/G]GAAGAACCGACAATT | 25831 |
rs566291952 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207581 | ACAGGGAAGCGAGAG[A/G]TTCTCGCGTGCGGCA | 25831 |
rs566292485 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203696 | GAAGGATTTTACATA[A/G]AGATAAATTTTATGT | 25831 |
rs566346048 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191488 | AGCCAAGATGACACC[A/C]CTGCACTCCAGCCTG | 25831 |
rs566420707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141056 | CCTCAGCCTCCCGAG[G/T]AGCTGGGATTAAAGA | 25831 |
rs566450534 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198960 | AGAACTGCTTGAATC[C/T]AGGAGGTGGAGGTTG | 25831 |
rs566461213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190811 | GCTGCGCCAGGCCCT[A/C]TTTTTTATACATTGA | 25831 |
rs566510356 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31168818 | GAGGCCGAGACGGGC[A/G]GATCACGAGGTCAGG | 25831 |
rs566527463 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192196 | ACTAAAAATACAAAA[A/C]TTAGCCGGGTGTGGT | 25831 |
rs566583025 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196558 | AGGAGTTCGAGACCA[A/G]CCTGGCCTATATGGT | 25831 |
rs566641567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112347 | GTCTTGACAGTATAG[C/T]TGTACATTTTCAACT | 25831 |
rs566654507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119080 | TGGCTCACTGCTCGT[C/T]GTCACTCTGACTCCT | 25831 |
rs566713177 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168428 | CTTTGTTTGTATCTT[C/T]CTTTTTCTTATCATC | 25831 |
rs566729270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119920 | GCAAAATTTCATTGT[C/T]GCAAAAGCAATGTGT | 25831 |
rs566773532 | snp | A/G | 1.66466e-05 | 0.00288496 | missense | HECTD1 | GRCh38.p7 | 14:31107181 | CACTATCCTGTGGAA[A/G]TGGTGCTGTGAACAG | 25831 |
rs566798146 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180613 | CCACACACAGCTAAT[C/T]TTTGTATTTTTACTA | 25831 |
rs566832477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206115 | TTTGGACGTAAGAGT[A/G]CTTAATGCAGTTTTT | 25831 |
rs566870645 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164227 | CTACACAGGTAATAG[C/G]TAATGTCAATATACA | 25831 |
rs566909100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137068 | ACCTCGTGATCCACC[C/G]TTCTTGGCCTCTCAA | 25831 |
rs566912458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163575 | TCCACTATACTCCAG[C/T]CTGTGCGACAGTGAG | 25831 |
rs566917111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192102 | GGACACTGAGACAGG[C/T]GGATCACCTGAGGTA | 25831 |
rs566999010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113705 | CTGCATTCAGATCCA[A/G]TGCTACCAGCCATAT | 25831 |
rs567018743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185189 | CCACTAAAAATACAA[A/G]AAATTAGCTGGGTGT | 25831 |
rs567169583 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171340 | CGTTTGAACACAGGA[A/T]TTCAAGGCTGCAGTG | 25831 |
rs567179456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169640 | AATCTCAGCACTTTG[A/G]GAGGCCGAGGTGGGT | 25831 |
rs567183171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162822 | GCAGTGGCTCACACC[G/T]GTAAACCTAGCACTT | 25831 |
rs567200508 | snp | C/G | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31100071 | GTACCTGCTAAAGCT[C/G]TTAAGTCTGATGACT | 25831 |
rs567226829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142473 | GAGTCTCGCTCTGTC[A/T]CCCAGGCTGGAGTAC | 25831 |
rs567244589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163464 | AAGAATTAGCTGGGC[A/G]TGGTGGTGCACAACT | 25831 |
rs567251801 | snp | A/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100271 | GCACTTAGACCAGGT[A/T]TTCCCCCCTTAATAC | 25831 |
rs567254252 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204138 | GTTTGCTTAATCCAG[C/T]CTATCATCGATCGAC | 25831 |
rs567298329 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137162 | GAGATGGGAGTCTTG[C/T]TCCTGTTGCCCAGGC | 25831 |
rs567347164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109136 | GGTAGAAGCCCTCAA[A/G]CAGAACAAGCACTTT | 25831 |
rs567358706 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31169717 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAATT | 25831 |
rs567382531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156174 | ATGGCGTGAACCCAG[C/G]AGGCGGAGCTGGCAG | 25831 |
rs567387778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141707 | AAAAAAACTTCAAAA[A/C]TTTTCCTCTTATTAT | 25831 |
rs567422027 | in-del | -/ATG | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134089 | AGGAGAAATTCTCTT[-/ATG]ATGGAAAAACGGACT | 25831 |
rs567453138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113641 | CAAGGCATTCTAAAC[C/T]ATTAAAATTCCCAAA | 25831 |
rs567494857 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199463 | CAGTGGGGCGATCTC[A/G]GCTCACTGCAAGCTC | 25831 |
rs567506025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200095 | CAGTGTTCTCTCTCA[G/T]TGAGTGGCATCATCA | 25831 |
rs567594290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151160 | CTATAATCTCTATAT[A/G]GATAATAGAGACAGG | 25831 |
rs567607508 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207371 | AGGCGCTCCCGCCTC[C/G]CCTTCCCGCAGGCTC | 25831 |
rs567612861 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132861 | AACAGTAAAAATGTT[A/C]ATCCTTTTTCTTCTA | 25831 |
rs567671352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200430 | GCGGGAGGATCACTT[A/C]AGCTCAGGAGTTCTA | 25831 |
rs567686060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158407 | ACTACAGGCGCACAC[C/T]GCCACGCTCAGCTTT | 25831 |
rs567697698 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206807 | AGTCATTACAAAAGC[A/G]CCCCGTAAGCGCCCT | 25831 |
rs567722810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31164850 | ATGGTAGCATACTTT[A/G]TAATTTTCTGATGGC | 25831 |
rs567724519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31120747 | TCTGGTTTCAGAATG[C/T]TTGGGTTTGCATCCT | 25831 |
rs567789368 | in-del | -/AAAAAC | 0.0267878 | 0.112589 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111982 | GAGACTCTGTCTCAA[-/AAAAAC]AAAAACAAAAACAAA | 25831 |
rs567809133 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102548 | GATTCTCCTGTCTCA[C/G]CCTCCCAAGTAGCTG | 25831 |
rs567906662 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171052 | CTCTTTGGACCTCAA[C/T]TTCTCTAACTGTAAA | 25831 |
rs567925460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124252 | TGAAATTCTATCTCC[A/G]GTATGTTACAACTGA | 25831 |
rs567925551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116969 | TAATGGAAATAATTA[C/T]ACCTACGTTACTGAA | 25831 |
rs567950918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135473 | GTAAAATGACTGACT[G/T]ACTTTGCATTTGTTC | 25831 |
rs567984344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203522 | CCTATAGTCCCAGCT[A/G]CTGAAGAGGCCGAGG | 25831 |
rs568033550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111839 | AATGCCATTAGCCAC[A/G]CGTGGTGGCGTGCAC | 25831 |
rs568059846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105221 | GGTCAGGCTGGTCTC[A/G]AACTCCCAACCTCAG | 25831 |
rs568071767 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103922 | CAGTGAGCCGAGTTC[A/G]TGCCATCACACTCCA | 25831 |
rs568160890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169000 | AGTGAGCCGAGATAG[C/T]GCCATTGCACTCCAG | 25831 |
rs568185063 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175660 | CTTGAGGTCAGGAGT[A/C]CAAGACCAGCCTGAC | 25831 |
rs568207976 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122395 | TGTGTGTGTGTGTGT[A/G]TGTGTCATTCTGTGG | 25831 |
rs568213071 | snp | A/G | 0.000264988 | 0.0115076 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129357 | CACTGTATCAGGGTC[A/G]TACCCTGGTGCAAGC | 25831 |
rs568243253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174038 | ATATTAATGGTACCT[A/G]TATCTCATTGTGTTA | 25831 |
rs568270105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140403 | AATGTGAAAATTTGA[A/G]TCAAGAACTTTCAAA | 25831 |
rs568270397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136885 | GGAGTGCAGTGGCGC[A/G]ATCTCGGTTCACTGC | 25831 |
rs568301812 | in-del | -/AG | 0.00795532 | 0.062565 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155908 | AATATTTAGGTTAAA[-/AG]GTAAAACTCTGTATT | 25831 |
rs568306339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167112 | AGGAGTTCAAGGTTA[C/T]AGTGAGCTATGATTG | 25831 |
rs568308514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174602 | TGAGATCTATCTTAA[G/T]TCAACAAAATCAGGT | 25831 |
rs568315223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181880 | ATCAAGGTTTCAAGG[A/T]AAATCAAAGAATGTC | 25831 |
rs568341215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138606 | TTATTCTGTCTGAAA[C/T]AAAACACAAAGTAGC | 25831 |
rs568348967 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164387 | AAGCTGGTCTCAAGC[A/G]ATCCTACTACCTCAG | 25831 |
rs568351156 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125925 | AAACAATTGGGATGG[A/G]GTGCAATGTTTTTGG | 25831 |
rs568395251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147269 | CAGTCAGCCGAGATC[A/G]CACCGCTGCACTCCA | 25831 |
rs568495561 | snp | C/T | 4.97541e-05 | 0.00498744 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133594 | TTGTCCACTGGCATT[C/T]TTCCCCATCTGTTTA | 25831 |
rs568532465 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195253 | TAAAATACACATACA[A/C]ATTTGACTGCAATTC | 25831 |
rs568553023 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117371 | ACGAGACTCCATCTC[-/A]AAAAAAAAATTTTTT | 25831 |
rs568619501 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104638 | GTTAATTCATCCTGA[G/T]CAAGTAATCTAGAAT | 25831 |
rs568641601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154685 | AGAGAGAGAGTTCCA[A/G]AAAATAAACTCGGAT | 25831 |
rs568651048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112329 | AATATATTCCCTCTA[A/T]CAGTCTTGACAGTAT | 25831 |
rs568669565 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209593 | AAGATATATCAGAAT[G/T]TAAATGATTAACTTA | 25831 |
rs568681276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190545 | AAGAGGTAATACTGT[A/G]TCTAAAGATTGATGA | 25831 |
rs568701017 | in-del | -/T | 0.306679 | 0.24349 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125174 | ATCAGTAGTTCTAAC[-/T]TTTTTTTTTTTTTTT | 25831 |
rs568712876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111884 | ACTCAGTGGGGCTGA[A/G]GCAGGAGAATCGCTT | 25831 |
rs568753171 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204135 | CACGTTTGCTTAATC[C/T]AGTCTATCATCGATC | 25831 |
rs568754857 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180170 | GCAAAACTCCGTCTT[-/A]AAAAAAAAAAAATCT | 25831 |
rs568767233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197300 | CAAAGTGCTGGGACT[A/G]CAGATAGGCATGAGC | 25831 |
rs568781702 | in-del | -/AACT | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133779 | CCTGTAGAAAAAATA[-/AACT]AACTTTCATATTAAC | 25831 |
rs568790487 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114625 | CCTCAAGGAGTATTT[C/T]TAAGAAAAAATGTTA | 25831 |
rs568826260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196736 | TCCAGCCTACACGAC[A/G]GAGCAAGACTCCGTC | 25831 |
rs568876293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190221 | GCTGAGGTCCCAGAT[A/G]TCGCAGAACAGAGAC | 25831 |
rs568909800 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195940 | AGACAGTGTTTCTCA[C/T]TCCAGCACTTCTCTC | 25831 |
rs568922334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125086 | GCTGGGATTATAGGC[A/G]TGAGCCACTGTGCCC | 25831 |
rs568935388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154796 | TCTTTCACCACCCTC[A/G]GGATTCTACAATTAT | 25831 |
rs568958454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118199 | TTAAGTAGAGACGGG[A/G]TTTCACCATGTCGGT | 25831 |
rs568962425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203580 | CGAGGCCAGACTGGG[C/T]AACATAGTGAGGCCC | 25831 |
rs568998648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134463 | GATTATATGGAGAGT[C/T]TATGGAAAGTTTATT | 25831 |
rs569035289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126533 | ATTTTACAAAGCTTA[C/T]GAATCTATTACACTT | 25831 |
rs569059720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167760 | CTGCCTAGAAAACTC[C/T]TAAGTATCCTTTAAA | 25831 |
rs569107061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174718 | TAAACATATATCACA[A/C]TTATAATCTTAAAAG | 25831 |
rs569126182 | snp | C/G | 0.000215605 | 0.0103806 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119890 | ATAAAATTTCACACA[C/G]AAACATAATAAGATG | 25831 |
rs569161758 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125271 | CCTCCGCCTCCCAGG[C/T]TCAAAAGATTCTGGT | 25831 |
rs569163116 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113691 | GCCATGGTCAAAGTC[C/T]GCATTCAGATCCAAT | 25831 |
rs569167784 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106137 | ATAACCATTTATCAA[-/AC]ACAGTTTACCAACAT | 25831 |
rs569185462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140464 | TATGCTGGAGTCCCA[G/T]CTACAAGGGAAGCTG | 25831 |
rs569208346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177061 | CAGCTTACTTTACAG[G/T]GAATATAGCAAAATA | 25831 |
rs569267170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169715 | GAGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 25831 |
rs569288919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205031 | TTTTCAATTACTTAT[C/T]ACTGGAGTTCAAAAC | 25831 |
rs569364473 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101405 | TTTTCTAAGGCAGCA[A/G]CAAGCCCCCTAAAAA | 25831 |
rs569365192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119251 | TCATAAGTTCCAGAG[G/T]TTAGAACCTGATTTT | 25831 |
rs569382041 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132415 | GCACTCCAGCCTGGG[A/C]AACAAGAGCGAGACT | 25831 |
rs569402131 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129649 | GCTATCTGAAAGTCT[A/G]TATTATTTAACTCTC | 25831 |
rs569402971 | snp | A/G | 3.3168e-05 | 0.00407221 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31113954 | TTAATTTCCAGTGGC[A/G]CAGGAAAGCAGCGTC | 25831 |
rs569473891 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176561 | ACAAAAAATTTGAGA[A/C]CTGCTGACCTAAAGC | 25831 |
rs569475387 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146903 | CTTTAAACAAAAACA[C/T]ACTAAAAAACAAGGT | 25831 |
rs569484605 | in-del | -/TC | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183378 | TGCTCTAAAGTTTAT[-/TC]TGTTATAAATTCAGT | 25831 |
rs569513902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185080 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATACCAGC | 25831 |
rs569541360 | snp | C/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150127 | GCATCACTCCAAATA[C/T]ATAAGCAGTCCCTTC | 25831 |
rs569543001 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110744 | CTGCCTCCCGGGTTC[A/C]AGCAAATTCTTATGC | 25831 |
rs569568493 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208120 | TGCGGCCCAACCTGT[C/T]CCCGCTGAGCCTTCC | 25831 |
rs569622593 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163486 | TGCACAACTGTGGTC[A/G]CAAGTGGTTGGGAGG | 25831 |
rs569644153 | snp | A/C | 1.65608e-05 | 0.00287752 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129312 | TTGCGTTGTGCCTGA[A/C]ACAGTGGATGAAACA | 25831 |
rs569672320 | snp | A/C | 0.000215337 | 0.0103741 | missense | HECTD1 | GRCh38.p7 | 14:31116305 | CAGGACAATTGAAGC[A/C]ATTTTTGTACATAGT | 25831 |
rs569677505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122316 | AGGCTGGAGTGCAGT[C/G]ACACAATTATAGCTC | 25831 |
rs569680861 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177201 | CTTGAATTTCTTTCA[C/T]CTGTAACAGAGAAAT | 25831 |
rs569761631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31130191 | TTGCCATAGAAATTT[C/T]AGTCACTAGTTCAAA | 25831 |
rs569800090 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183365 | GAACAGGTAAATTTG[A/C]TCTAAAGTTTATTCT | 25831 |
rs569807852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201713 | TGGGGTTTCACCATG[C/T]TTGCCAGGCTGGTCT | 25831 |
rs569857747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180915 | TCTTAAGCCTTGTTA[C/G]AGCATACTACATATG | 25831 |
rs569862355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187328 | ACGCCACTGCATTTC[A/G]GCCTGGACGACAGAG | 25831 |
rs569894250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101990 | ATTTTTATTCCAGCA[A/T]AATAATTATCTTGTG | 25831 |
rs569911162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151886 | TCAAACACTAAAGAA[C/T]AGTCAATGCAGGACT | 25831 |
rs569976264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159479 | AGAGTAGTTGTGATT[A/T]CAGGTGTGCACCACC | 25831 |
rs569999220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193557 | AGCATAAGTCCTTTG[C/T]ATTTCCATATAAATT | 25831 |
rs570020776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139429 | TAGAAGGTTCCATCT[A/G]AGAGGAATAGGCCCT | 25831 |
rs570036608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159854 | CACGTTGCCCAGGCT[A/G]GTCTCGAAATCCTGT | 25831 |
rs570041469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182447 | ATCTGTCCACCTCAG[C/T]CTCCCAAAGTGCTGG | 25831 |
rs570050143 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187160 | GAGACCAGCCTCGCC[-/A]AATGTGGCAAAACCT | 25831 |
rs570197650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187073 | AAAAAACAGGCCTGG[C/T]GTGGTGGCTCACGCC | 25831 |
rs570202421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131179 | GCAAAACTAAATTTC[C/T]ACATTTGTCAGATTA | 25831 |
rs570244243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103419 | TGGTGGCGGCTGCCT[A/G]TAGTCCCAGCTACTC | 25831 |
rs570255004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152757 | AAAGAGGCCAGGTGC[A/G]GTGGATCACTTTGAG | 25831 |
rs570270798 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153283 | TGTAGTCCCAGCTAC[A/T]CGGGAGGCTGAGGTA | 25831 |
rs570322031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122746 | TTATTTTCTTTAAGT[A/G]GAGAATCATAAATGC | 25831 |
rs570358563 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208695 | TTTTACTCTCTTGAG[A/G]CCCGGAGTTCGAGAC | 25831 |
rs570375978 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138046 | TTCTACAGGATAAGC[A/T]TCCCTAATCTACAAA | 25831 |
rs570402297 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116808 | GATAATTTTTGTATT[C/T]TTAGTAGAGACGGCA | 25831 |
rs570406401 | in-del | -/TGT | 0.00119784 | 0.0244435 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146926 | AACAAGGTGAAAAAA[-/TGT]TGTCACAACAGGCCT | 25831 |
rs570406774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31166288 | GCAAACACCCATTCA[A/G]AAGATCTAGGGACAG | 25831 |
rs570432038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111440 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACCAC | 25831 |
rs570475450 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209436 | TAAGAAGACTAATTA[C/T]GGAAAGTGTCTAGAA | 25831 |
rs570477067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31201940 | CACTGACACATCATA[A/G]AAGAAGTTATATTCG | 25831 |
rs570488676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182999 | CAGCCACTGATTTAC[A/G]GCAAATACAGCCAAA | 25831 |
rs570492258 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162433 | CCCCTGAATGATCTG[A/C]GAAACATCCATTATA | 25831 |
rs570492421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174801 | GGATGGAATTACCTC[A/G]ATTTCATCAAGTGAA | 25831 |
rs570513474 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159888 | CAGGAGATCCACCCT[A/G]CTCGGCCTCCCGAAG | 25831 |
rs570538540 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104566 | GCAAAACTGTGTTCT[A/C]ATTTTCAAAAGTAAT | 25831 |
rs570541614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167048 | CAAGGCGGTATACAT[A/C]TGTAGTCCTAGCTAC | 25831 |
rs570591962 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153844 | AAAAGAAATGATACA[A/T]ATATATATATATGTG | 25831 |
rs570598247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173047 | GGGAGAATATCGAAG[G/T]GGTGCCACTTTGTTA | 25831 |
rs570608952 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160722 | GTCATCTAGACTGGA[A/G]TGCAGCAGCACAATC | 25831 |
rs570654888 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117245 | GGACATGATGATGCC[C/T]GCCTGTAGTCCCAGC | 25831 |
rs570685130 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189909 | CTTTCCTCTTGAATC[C/T]GAGCAGGCTTATGAT | 25831 |
rs570722416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188004 | CAGGTGATCTGCCCA[C/T]CTTGGCCTCCCAAAG | 25831 |
rs570724019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145252 | AACAGAAAAAAACGT[A/C]TCTCTCTAAACTACT | 25831 |
rs570744797 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192914 | CCCAGGAGGCGGAGG[C/T]TGCAGTGAGCCAAGA | 25831 |
rs570761658 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185903 | AGAAAAAATATTCAC[A/C]TTATCAGGAAATTTG | 25831 |
rs570783307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125732 | TCAAATTCTTGCTAT[A/G]AATTAGGAGAGGCTA | 25831 |
rs570795120 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153349 | GTGAGCTGAGATCAC[A/G]ACAGAGCGAGACTCC | 25831 |
rs570867129 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125111 | GTGCCCGGCCAACAA[A/T]AAATTTTTTTAAGGC | 25831 |
rs570890359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186469 | GAGCCGGGTGGATCA[A/C]CTGAGGTCAGGAGTA | 25831 |
rs570909999 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181619 | ACCCTGTCTCAAAAG[-/A]AAAAAAAAAAAAAAA | 25831 |
rs570985174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147134 | CTGGCTAACACAGTG[A/T]AACCCTGTCTCTACT | 25831 |
rs570990655 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158307 | GTTGTCTCGGCTGGA[A/G]TGTAGTGGCACAATC | 25831 |
rs570993970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132162 | GGTGTAAGTTGCCGC[A/G]TGCGGTGGCTCACGC | 25831 |
rs571015715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195867 | TCTGGTAATCGTCAC[A/C]AAAGCTCCCTGAATT | 25831 |
rs571100636 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111807 | TGGTAAGAATCTTGC[C/T]CTTGTTTGTTTACAA | 25831 |
rs571124135 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141408 | TTCAAATTTTCAACT[A/C]TCTTAAACAGGCATG | 25831 |
rs571149630 | snp | A/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208699 | ACTCTCTTGAGGCCC[A/G]GAGTTCGAGACCAGC | 25831 |
rs571169808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164171 | GCCTTCACTGATCTG[C/G]TGTCTGCCTTTTATT | 25831 |
rs571196275 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156202 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 25831 |
rs571214243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127324 | AGTTTTTTCATATTA[C/T]ATATAAAGATTCTGT | 25831 |
rs571219508 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193465 | CATTGTCTTTATTAC[C/T]GTAGCTGTATAATAA | 25831 |
rs571231002 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31142678 | ATTCCTGACCTCAAG[C/T]GTTCTGCCCACCTCA | 25831 |
rs571232531 | snp | C/T | 1.65968e-05 | 0.00288065 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156896 | AAGGACCTGCCAACG[C/T]TGACACTTTGCTAAT | 25831 |
rs571286450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102155 | GCAAAACTGATCAAC[A/G]TATGGTGATTAGATT | 25831 |
rs571294768 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104173 | ATTTCAAAGAAGCTA[A/G]AAGAGAATAATTTGA | 25831 |
rs571311452 | in-del | -/ATTT | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140231 | TAAAGCAGATGTATG[-/ATTT]ATTTTTAAAGTTTAA | 25831 |
rs571314482 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182208 | CTCTTTTTTTTTTTT[C/T]CAGACAGGGTCTTGC | 25831 |
rs571332607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143324 | GAGGCTAAGGCAGGA[A/G]AATCACTTGAGCCCA | 25831 |
rs571346442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198951 | TAAGGCGGGAGAACT[A/G]CTTGAATCTAGGAGG | 25831 |
rs571441548 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31198930 | AGTCCCAGCTACTCA[A/G]GAGGCTAAGGCGGGA | 25831 |
rs571448592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109260 | TGCTCTGCCAGAGGA[A/G]AAGGCTTCTGCCTAC | 25831 |
rs571459398 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206884 | GGAAGCCGGCGGCGG[A/G]GCGCGGTGGGCACCC | 25831 |
rs571483223 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100418 | GCCAAACAAAGAGAG[A/G]ACACTAGAATACTCT | 25831 |
rs571512289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108409 | CTGCTTATTTCTGAG[C/T]TAAAGACACTTTAAA | 25831 |
rs571513517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144573 | AATTATATGGATACC[A/G]AAATCTGATTTTCAT | 25831 |
rs571520470 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207508 | GCAGGTCGAACCGGG[C/T]AGGCGGCACAGGAAA | 25831 |
rs571541943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149596 | CAAAAGAAATTGATA[C/T]TAAAAAATAAAGAAA | 25831 |
rs571593552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205730 | TACACAAACTGAAGT[C/G]AGCAAATGGTTGAAA | 25831 |
rs571605513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200891 | CTGAGCTTTTCCTTC[A/G]TGACATTTAACACAG | 25831 |
rs571610663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106247 | AAAGTAACAGAGTTT[C/T]ATCAAAAGTTCTGCA | 25831 |
rs571615967 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194234 | ACCAAGTGCCAGGCA[C/G/T]TGGGATGGGGAAAGG | 25831 |
rs571669943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187502 | CAGCATATCTGGAAA[G/T]AAGAGGAGATCATTC | 25831 |
rs571676815 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200483 | AGACCTTGTCTCCAT[C/G]TAATTTAAAAAAAAA | 25831 |
rs571677882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206422 | AGTATTTTGAGGAAA[C/G]TCTAAACACCTTGAT | 25831 |
rs571709252 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184501 | GCTGAGGTGGGAGGA[C/T]GGCTTGAGTCTGAGA | 25831 |
rs571715028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114885 | ATTTTTCCTAGGCCA[C/T]GAACCTTAACAGCAT | 25831 |
rs571793968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152049 | AAAGTTTGAGGCAAC[C/T]GGAATATGTGGAGGC | 25831 |
rs571799562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171117 | TAGTGATTCTTCTAC[A/G]AACAGAGTATTTGGC | 25831 |
rs571836138 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165572 | CCATCATAGGTTATA[A/C]AAAGCTCCTCTCTAC | 25831 |
rs571862478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165102 | CAGTGAATTATTTTG[C/T]GGCCAGTTCTCTCCT | 25831 |
rs571876830 | snp | A/C/G/T | 0.000132741 | 0.00814583 | missense, nc-transcript-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121394 | TTACCTGCTCCCCAA[A/C/G/T]AGGTCGGCTCCCTGC | 25831 |
rs571889053 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206540 | ATATCCAAATACAAA[C/G]GACAATTATATACAA | 25831 |
rs571895900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157982 | AAATTTCCTATAATC[C/T]AAAATACAATGCTCT | 25831 |
rs571916729 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169947 | TAATTGTACTTGGTT[A/T]TTTATCATCATCTCA | 25831 |
rs571918627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178398 | TAGGTAATATTTCTC[A/G]CATTGTTTTTGCTTC | 25831 |
rs571921780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114601 | ATTAAGGTGTGTCAC[A/G]ACACCCAGCCTCAAG | 25831 |
rs571963140 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185735 | CTGTTTAAAAAAAAA[-/AAG]AAGATAATTCAACTT | 25831 |
rs571963327 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31109167 | GCCACCTCAAGAGTG[A/G]AGATCTTCTTTGTTG | 25831 |
rs572016817 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174502 | GTGAGCCAAGATCAT[A/G]CCACTGCACTCCACC | 25831 |
rs572052173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165171 | AATACTGGTATTTGA[A/G]GTACTTGAATCTTAT | 25831 |
rs572069396 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194899 | CAGAAGATTGGCAAA[A/G]ACATGAAAGAATATA | 25831 |
rs572125608 | in-del | -/TTT | 0.00953873 | 0.0683987 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160677 | CTAGTAAGGAAATAC[-/TTT]TTTTTTTTTTTGAGA | 25831 |
rs572141413 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141656 | CATTCATACCAGACA[C/T]GTAATTTCAATGTTT | 25831 |
rs572167460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127396 | CGCTCTTGTTGCCCA[A/G]GCTGGAGTGCAATGG | 25831 |
rs572204731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186026 | CTTCAATTTTCTCTC[A/G]ATTTATGACTCCCCT | 25831 |
rs572229115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126926 | TCCTCCCACCTTGGC[A/G]TCCCAAAGTGCTGGG | 25831 |
rs572230906 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146328 | CTCTTTCTTGCTTCA[G/T]GTCTCATACTATAAA | 25831 |
rs572272765 | snp | A/G | 1.95865e-05 | 0.00312936 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134839 | CAAAGCTCTTTAGTG[A/G]GTTTTCCAATTTGCA | 25831 |
rs572288945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165832 | AAACCCCCCAAAAAC[C/T]AGTATTTCAGAGAGT | 25831 |
rs572307661 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205288 | AATTTTCTACTCTTC[C/T]GCTACACGGTTAAGA | 25831 |
rs572316473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134661 | AGTGTAAAATAGCTC[A/G]GCTTTCTATTATTTA | 25831 |
rs572320571 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191846 | TCTGCTAAAAATACA[-/A]AAAAAAAAAAAAATT | 25831 |
rs572322105 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112611 | ATGCATTCATTCATT[C/T]GTTCATTTTTTTTTT | 25831 |
rs572329611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193721 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 25831 |
rs572365695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129750 | TCCTTTTATTTCCCT[C/T]ATTTCTGAACTATTC | 25831 |
rs572397851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180372 | GCAACATGGCAAGAC[C/T]CACTATTAAAAAAAT | 25831 |
rs572444340 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151148 | TAAAGACACTATCTA[C/T]AATCTCTATATAGAT | 25831 |
rs572452134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200234 | ACTTTCTACTTTTAT[C/G]ACAAAACCCTCTATC | 25831 |
rs572478375 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172381 | GGCCGAGGTGGGAGG[A/T]GGTCAGGAGTTTGAG | 25831 |
rs572538875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31187563 | GAACAGGACATTTGT[G/T]CAATGGAATGTCCCA | 25831 |
rs572661216 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178851 | ACCTCAAACATGAAC[C/T]GCTCTATGAAACCCT | 25831 |
rs572682436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206950 | GGGCCCGGCCGAGCC[A/G]GGCGCTGAGAGGCGC | 25831 |
rs572694434 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190075 | TTGAGAGTCCACATG[C/T]AGGTGTTTCAACTAA | 25831 |
rs572705857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132957 | TAAAATAAAACTCAC[A/G]GTAAGCTTGAAAATA | 25831 |
rs572744273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150569 | ACTAAATCTTACAAA[C/T]AAGTGTTAAAAATAT | 25831 |
rs572781863 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130461 | CTTTTTTTAAAAAGG[C/T]AATTAACTTCCAAAA | 25831 |
rs572850867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203020 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAA | 25831 |
rs572870548 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140544 | TCTGGCACCCGTAAA[C/T]AGCCACTGGACTCCA | 25831 |
rs572874658 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183200 | TATATAGAATTTGTT[A/C]TATTTTATTTAAAAT | 25831 |
rs572885289 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175812 | GAGGTTGTCGTGAGC[C/T]GAGATCGCGCCACTG | 25831 |
rs572886614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190247 | GAGACAAGCCATCTC[C/T]ACTCTACCCTTTCCA | 25831 |
rs572946903 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170182 | TTTGGGAGGCTACAC[C/T]GGAGGATCACTGGAG | 25831 |
rs572946908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149658 | CTGTAACTCCAGCAC[A/G]TTGGGAGGCCGAGGT | 25831 |
rs572980367 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162139 | CGGGAGGCTGAGGCA[C/T]GAGAATCGCTTGAAC | 25831 |
rs573008561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182776 | GAATGGCATGAACCC[A/G]GGAGGCAGAGCTTGC | 25831 |
rs573019428 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156370 | CTGAGGTCAGGAGTT[G/T]GAGACCAGCCTGACC | 25831 |
rs573057776 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191110 | CCCAAAGCACTGGGG[C/T]TACAGACCTGAGTCA | 25831 |
rs573120391 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31147497 | CACAGTGGCAAATGC[C/T]TGTAATCCCAGCACT | 25831 |
rs573144756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153604 | AACCTTTTGAAGTTT[A/G]ATTTACAAAATCTTT | 25831 |
rs573152513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191237 | ATTTCCTTAGTATGT[C/T]ATGACCGGCCAGGTG | 25831 |
rs573174974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106336 | TTTGCAAAGTGAATC[A/T]TATATTAGCAGATGA | 25831 |
rs573180658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191851 | CTAAAAATACAAAAA[A/G]AAAAAAAATTAGCCA | 25831 |
rs573200364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125305 | TTAGCCTCCTATGCA[G/T]TTAGGACTGCAGGAG | 25831 |
rs573237240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118644 | CACGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 25831 |
rs573302712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105830 | CCCCTCTCCTCCTCC[A/T]ACAAAATCAGTACAC | 25831 |
rs573337227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169205 | AAGCTGTTAAACAGG[C/T]TTATTAAATATAAGG | 25831 |
rs573358809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112627 | GTTCATTTTTTTTTT[G/T]GAGACAGAGTCTCAC | 25831 |
rs573359751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204540 | GACAAGTATGATTTT[C/T]AAAATACCAAAAGTA | 25831 |
rs573368806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161994 | CAACACTTTGGGAGG[C/G]TGAGAAGGGTGGATC | 25831 |
rs573400338 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163104 | ACACACGCACACATG[C/T]GCACACACACACACG | 25831 |
rs573423555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197849 | CAGCTCTCATTAAGA[A/T]CAATGACCTTGAGAA | 25831 |
rs573459967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190297 | TCTGTTAGCATAATT[A/C]TTGTTTAATACTACT | 25831 |
rs573521042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31190921 | CCTCCCAAAGTGCTG[C/T]GATTACAGACATGCC | 25831 |
rs573548559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31176690 | GTAATCCCAGCAGCA[C/T]TTTGGGAAGCCGAGG | 25831 |
rs573643079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196961 | CAGGTCCAATATAAG[C/T]AATCTCTTCAATTCA | 25831 |
rs573688981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169270 | AGTTCATTTATATAA[C/G]GTTAATGTGTCTACA | 25831 |
rs573692743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125354 | TAATTTTTTGTACTT[C/T]AGTAAAGAGGGTTTT | 25831 |
rs573715037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175979 | ATTATAGTCTTTTAT[G/T]TATAGTCTTTAAAAA | 25831 |
rs573734192 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197216 | AATTTTTAAGACTAT[A/C]ACTCAGGGCCAGGCA | 25831 |
rs573735054 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31140364 | TCATTATTAGTGTAA[A/G]CTGCAATGACACTTC | 25831 |
rs573781988 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130886 | ACCAACATTTAACTA[C/T]CTCTTCTGCTACACA | 25831 |
rs573819758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155083 | AGGAGCAGTGACTCA[C/T]GCCTGTAATACCGAC | 25831 |
rs573859782 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162889 | TCTGGGCAACATAGT[A/G]AGACCTTGTTTACAC | 25831 |
rs573861174 | snp | A/T | 3.50318e-05 | 0.00418505 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113835 | CAAAACAAAGCACGA[A/T]GCCATTTGCAATCAA | 25831 |
rs573897537 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194806 | GGTTCCAAAGAGAAA[A/G]AATTTCCCTGGGAAC | 25831 |
rs573901853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104931 | GATCCTCCTGCTTCA[C/G]CCTCCCAAAGTGCTG | 25831 |
rs573983080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119435 | TAGAAAATACAGTAA[A/G]AATTTCCCACCTTTA | 25831 |
rs574021939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119945 | ATGTGTTATTTAGAA[C/T]TACTGCATTTCCTTA | 25831 |
rs574029975 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202330 | AGACTTCAAAGGCTA[C/T]CACACAACTATTCAG | 25831 |
rs574068135 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206361 | CAGCAAACTTCATCC[C/G]CCTCCTTCTCTACCC | 25831 |
rs574082788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150334 | TTAAATACTCTGAAC[A/G]TAATACTCAATTGCC | 25831 |
rs574085616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186051 | TCCCCTGGTTTTCCA[C/T]TCTAGCTTCCTTCCT | 25831 |
rs574088649 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31100086 | CTTAAGTCTGATGAC[C/T]GCATTGAAATAGTCA | 25831 |
rs574135452 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155975 | GTCTCAGGCCGGGTG[C/T]GGTGGCTCACGCCTG | 25831 |
rs574137760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31146578 | CAATATTAATAAATC[A/T]ACAATACATATCAGG | 25831 |
rs574139494 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138389 | TTAAAGATTTATATG[G/T]GCATTTCGGTAGTTT | 25831 |
rs574196178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206310 | AAAGTCTATGCCAAA[A/G]GGCAAAGAACACCTA | 25831 |
rs574200036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156425 | TAAAAATACAAAATT[A/T]GCCAGGGAGGTGAAG | 25831 |
rs574265297 | snp | A/C | 1.71428e-05 | 0.00292765 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116486 | AAGATGGGTGAAAAA[A/C]AATTATACTAAAACA | 25831 |
rs574267763 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126748 | AGTGCAGTGGCATGA[C/T]CACAGCTCACTGGGG | 25831 |
rs574310325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31188284 | TCTGTCGCCCAGGCT[A/G]GAGTGCAGTGACACA | 25831 |
rs574316996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31204584 | CTCTAATGAAATCTA[C/T]GAACGCAATTTTTAA | 25831 |
rs574357132 | in-del | -/CTGG | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111546 | TGTGAGCCACCGCGC[-/CTGG]CTATTTTTTTTAAAC | 25831 |
rs574362445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163191 | ACTTTGGGAGGCTGA[C/T]GTCGGAAGATCGCTT | 25831 |
rs574389497 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122455 | AGCTCATGGCAGCAC[A/G]AGCCACTGCACTAAG | 25831 |
rs574442596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31195325 | TGCTAAGTGTTGGGG[A/G]TGGGACACAAAGATG | 25831 |
rs574453399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31153418 | TCACCATGTTGCCCA[A/G]ACTGGTCTCGAACTC | 25831 |
rs574509324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196285 | GCCTCCCAAAGTATC[A/G]GGATTACAAGCATGA | 25831 |
rs574520706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110034 | TGAGATGGAGTCTTG[C/T]TCTGTCACCCAGGCT | 25831 |
rs574531054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159068 | TGCAGATATCATTAC[C/G]CTTGAGGTGAATGAT | 25831 |
rs574544905 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208250 | CTGGCGGTTCACCCC[A/C]AAGAAAACCCTTCAG | 25831 |
rs574587142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110916 | AATTATAGGCATGGG[A/C]CACCGTGCCCAGCCT | 25831 |
rs574651101 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207775 | GAAGCTGCCGAGGGC[A/C]GCCGAGCCCGGCGGA | 25831 |
rs574664563 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31123683 | TGGATCTGGAAAAAA[C/T]AGTAAAATATAATAT | 25831 |
rs574692828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174405 | CAAAAATTAACCAGG[C/T]GTGGTGGTGGGCACC | 25831 |
rs574731080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203163 | CAGAGGCTAATGAAC[A/G]CAACAGACCAAGAAT | 25831 |
rs574753873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173087 | CTAAGAGTACTGTCC[A/G]AAAACTAGAAACTGC | 25831 |
rs574761421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31160955 | GATTACATGCATGAG[C/T]TAACACACCCAGCTA | 25831 |
rs574770686 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139040 | TTACATATTATATAC[A/C]GATATATATATATAT | 25831 |
rs574777638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31104290 | AATGCCCCATAAACA[C/T]GTACATATATTATGC | 25831 |
rs574785724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161777 | ACAAAAAAATTAGCC[A/G]GGCATGGTGGTGTGT | 25831 |
rs574795234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159055 | CTAGGCACTAAGCTG[A/C]AGATATCATTACCCT | 25831 |
rs574804461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31154421 | TCCTGCCTCAGCCTC[C/T]GGAGTAGCTGGGACG | 25831 |
rs574827075 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124774 | CTGAATCTAAAATAA[A/T]AATTATATTAATTTT | 25831 |
rs574881851 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170147 | CCAGGTGTGGTAGCT[A/C]ACGCCTATAATCCCA | 25831 |
rs574888395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132229 | GATCACCTGAGGTCG[A/G]GAGTTCAAGACCAGC | 25831 |
rs574897803 | snp | C/G | 0.000399281 | 0.0141238 | missense | HECTD1 | GRCh38.p7 | 14:31112531 | GAGCCCCACTTGCCA[C/G]TGCCAATGGTTCCTG | 25831 |
rs574929381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123955 | GGTTGAAAGGTCTAC[A/G]TTTTTAAAACATTGT | 25831 |
rs574934121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139751 | TCAATCAAATGGCAT[A/G]TAAGCTAAAATCTTT | 25831 |
rs574936036 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124251 | TTGAAATTCTATCTC[C/T]GGTATGTTACAACTG | 25831 |
rs575013812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117760 | CTAATATTTAAAATT[A/G]CCAATGGCAACAACA | 25831 |
rs575019397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139165 | CTGACATAAAGACCC[A/G]AAAAAAATTGTGCTT | 25831 |
rs575035975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103976 | TCCGTCTCAAAAAAA[C/T]AAAAACAACAAAGTT | 25831 |
rs575063048 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111552 | CCACCGCGCCTGGCT[A/T]TTTTTTTTAAACACT | 25831 |
rs575093602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131658 | GGGAAAAAAAAAAAG[A/T]TTCTAATTTCCCTAT | 25831 |
rs575097839 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202181 | TCCAGCCTGGGTGAC[-/A]AGAGCGAGACTCTGC | 25831 |
rs575100222 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103564 | AAAAAAGAATGAAAT[A/C]TTTTCATTTGTAGGA | 25831 |
rs575107394 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193740 | ACCAGCCTGGCCAAC[A/G]TGGTAAAATCCTGTT | 25831 |
rs575113856 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182191 | GAGCCACTGCGCCCA[A/G]CCTCTTTTTTTTTTT | 25831 |
rs575174670 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161716 | CGAGATGAGGAGTTC[C/G]AGACCAGCCCAGCCA | 25831 |
rs575191276 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31107876 | TTTTAATTTTCCTAA[A/G]GAGTCCACTTGTTGT | 25831 |
rs575283088 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197498 | CCAACAGTTTCTGCA[C/T]AATCTAGGACCATAT | 25831 |
rs575287327 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31161859 | CTGTGCAACAGAGCA[A/G]GACTCTGTCTCAAAA | 25831 |
rs575311545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31182692 | TCTCATCTCTACTAA[A/G]AATATAAAAATTAGC | 25831 |
rs575312738 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190675 | CCTTAAACACCATAT[A/G]CTTGGCTAACTTTTT | 25831 |
rs575344763 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155215 | CTGGGCGTGGTGGTA[C/T]GTGCCTGTAATCCCA | 25831 |
rs575364647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31202984 | GTCCCAGCTACTCGG[A/G]AGGCTGAAGCAGGAG | 25831 |
rs575442179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123750 | TATTCCTGAAGAACA[G/T]CCAGAAGACAATTTA | 25831 |
rs575479060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117040 | TCTCATTTTTACATG[A/C]AAATAATACTAACTG | 25831 |
rs575511068 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132274 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAATT | 25831 |
rs575544491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31197012 | TAGCTATTTGTGTGC[C/T]AGGCACTATGCTTAG | 25831 |
rs575547746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31132916 | TATGGTGTGAGACTA[A/T]CAAGATAAAGAAAAA | 25831 |
rs575561266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167166 | GACAGAGCAAGACCT[A/G]TCTCTAAAAATAAAT | 25831 |
rs575619458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158178 | TAGTATGCCTCCTTT[C/T]CCTTTTATTCACTTA | 25831 |
rs575641275 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31118518 | ATGAAGAAATTCAAG[C/T]TTGGATAGTTTTGGT | 25831 |
rs575675816 | snp | C/G/T | 4.99641e-05 | 0.00499799 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102903 | GTTGATCTTGGAAAA[C/G/T]AGTATCACATACCTG | 25831 |
rs575677648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105026 | TTTTTTTTTGTGCAG[C/T]GGAGTTTTGCTCATC | 25831 |
rs575681170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31158940 | CAGAGCCAGACTCTG[C/T]CTTAAACAAAAACAA | 25831 |
rs575703007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31125257 | GTGGCTCAATGCAAC[C/T]TCCGCCTCCCAGGTT | 25831 |
rs575705778 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31165185 | AGGTACTTGAATCTT[A/G]TAAAACTGCCTGCTC | 25831 |
rs575725236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175693 | ACATGGAGAAAACCT[A/G]TCTCTACTAAAAAAT | 25831 |
rs575731842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203895 | TAATGCTATCCCTCC[C/T]CCCTCCCCCTACCCC | 25831 |
rs575794995 | snp | C/T | 0.000140637 | 0.00838444 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106180 | ATTAAAAAAAAAAGG[C/T]CTTGCAGTTAACCTA | 25831 |
rs575906880 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135919 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATCAC | 25831 |
rs575910268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31124946 | CTGAGAAGCTGGGAC[G/T]ACAGGGATCCGCCAC | 25831 |
rs575933138 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142328 | ATCAAAACTATTTCA[C/T]AGATTACTAAGTGAT | 25831 |
rs575946717 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207625 | GTCCAGTCCCCAGCA[A/C]GCGGCTCCTCAGGCC | 25831 |
rs575950294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101753 | GCTGAGATTGTGCCA[C/T]TGCATTCCAGCCTGG | 25831 |
rs575950558 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186321 | CATAGTAAATGTCAA[-/C]CCATCCAGAAAGCCA | 25831 |
rs575974382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151718 | TTTTTAAAAAAAATG[A/T]ATAAACATTTTGTAG | 25831 |
rs575977484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31183171 | TGAAAACATATACAT[C/T]AAAAAAAATAAATTA | 25831 |
rs575996322 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31168834 | GATCACGAGGTCAGG[A/C]GATCGAGACCATCCT | 25831 |
rs576004717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200674 | TAATTCCAGTTACTG[G/T]GGCGGCTGAGGCAGG | 25831 |
rs576058989 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185780 | TATTGGACAAGCACT[A/C]GACTACCTTCTATGA | 25831 |
rs576070716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115623 | AAATTAGCTAGGCCT[C/T]GTGGTGCACACCTGT | 25831 |
rs576070918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31108612 | GTGGATCACTTGAGC[C/T]CAGGAGTTTGAGACC | 25831 |
rs576109725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109643 | GCATACGTTAACAGC[C/T]GAATGTACTACTAAA | 25831 |
rs576111704 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148162 | AAAAAAATGCAAGAA[C/G]AATAAACATGGAAAT | 25831 |
rs576112061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121038 | CATTAAGCGTTAGCT[A/G]TTAATAAACTACTAC | 25831 |
rs576143588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128599 | CGGATTCCAGAAGGA[A/G]AAGCTCACTTACTTG | 25831 |
rs576183979 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179277 | TACAAAAATTAGCTG[G/T]GCATGGTGGCACATG | 25831 |
rs576220099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31194469 | ATACTTCTAGGCACA[A/G]AATTTTATATATAAT | 25831 |
rs576222535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178622 | GCCTGCCCAACATGG[C/T]GAAACCTCATCTGTA | 25831 |
rs576225998 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203508 | GTGTGGTGGCACAGC[A/C]TATAGTCCCAGCTAC | 25831 |
rs576334375 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115534 | GAGGCTGAGGTGGAC[A/G]GATCACTTGAGCTCA | 25831 |
rs576359888 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31193838 | CTGAGGCAGAAGAAT[A/C]GGTTGAACCCGGGAG | 25831 |
rs576373191 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142519 | GCTCACTGCAACCTC[A/G]CCTCCCAGGCTCAAG | 25831 |
rs576393310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143473 | ATAAAGAGACATTCT[G/T]AAATCGAAAAAATAT | 25831 |
rs576398625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174154 | TGATAATCTATGATA[C/T]CAACTGAAAATAACA | 25831 |
rs576435730 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129793 | TTAAAAGCAATGTAA[C/G]GGTCATGTTTAAATC | 25831 |
rs576446455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181261 | TAATTTGGGGAATAA[C/T]AGTTCCTGCTGTGTT | 25831 |
rs576469631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119627 | AAAATTTTTAATAAC[A/G]TGCATACAAAAGCAA | 25831 |
rs576477319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152894 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACC | 25831 |
rs576483558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159002 | AGAGCCAATAATCAA[C/T]TCATTTAACAAATAT | 25831 |
rs576546751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31159585 | CCTCAGGTGATCTGC[C/T]TGCCTCAGCCTCCAA | 25831 |
rs576551653 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148144 | TTTTTTTTAAAAATG[-/A]AAAAAAAAATGCAAG | 25831 |
rs576554634 | snp | C/G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185138 | ATGAGGTCAGGAGAT[C/G/T]GAGACCATCCTGGCT | 25831 |
rs576640798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31152255 | AGTAGAAAATCCTCA[G/T]AGATCACCAGGATAT | 25831 |
rs576713286 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102532 | CCTCTTGGGTTCAAG[A/T]GATTCTCCTGTCTCA | 25831 |
rs576724470 | snp | A/G | 4.96997e-05 | 0.00498472 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128689 | AGATTCATGTTGTTC[A/G]TGGCATTAGTCCGTG | 25831 |
rs576732114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31111292 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 25831 |
rs576763377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129646 | CTAGCTATCTGAAAG[C/T]CTATATTATTTAACT | 25831 |
rs576799728 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209136 | AATTATTTAGATGTC[A/G]TGAGTGTGAATTGGA | 25831 |
rs576809202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145070 | TGTCATTTGGGCACA[A/G]ATGAGCTCTCGAAGT | 25831 |
rs576892844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174302 | CTGTAATCCCAGCAC[C/T]TGGGGAGACTGAGGT | 25831 |
rs576916777 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109899 | AGCCCCAACATCATT[A/C]AAAAAAAGGAAAAAT | 25831 |
rs576924835 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31155951 | AATTTTTTTTTTTTT[-/A]AAGATGGAGTCTCAG | 25831 |
rs576934199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31115222 | TAGCTCTTGGGAACT[C/T]GGGGAAAAAAAACTG | 25831 |
rs576949227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172360 | TGTAATCCCAGCACT[C/G]TGGGAGGCCGAGGTG | 25831 |
rs576957228 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204438 | GACTTTTTAATGATC[A/G]GGCAACACTTTTTTA | 25831 |
rs576999336 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207694 | CGGCGGCGGCGCGGC[A/G]GGGAGGCCCAGTCCA | 25831 |
rs577013190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31181328 | TAAAGAGCCAGTTTA[C/G]GCTGGGTGCAGTGGA | 25831 |
rs577063577 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31110976 | TTTTTTGGTAAATTA[C/T]TTCTTCCATGATTAG | 25831 |
rs577064712 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | HECTD1 | GRCh38.p7 | 14:31203272 | GGACAATTTTCCCTT[-/G]TAACAACAAGAAAAT | 25831 |
rs577096233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121909 | ATATTGAGAGTTCTG[A/G]ATCACATTGCCTATG | 25831 |
rs577138616 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HECTD1 | GRCh38.p7 | 14:31117197 | TGGGTAACACAGTGA[A/C]CCCCGTCTCTACCAA | 25831 |
rs577177264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31180300 | TAGGGCCCGTATGGC[A/G]GCTCACACTTGCAGT | 25831 |
rs577194499 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150964 | AGCTGAGGGTGGTAG[G/T]GCGCACCTGTAGTCC | 25831 |
rs577232091 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108892 | GTATATGAAATAAAA[C/T]CAACAATGTCCACAG | 25831 |
rs577266960 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECTD1 | GRCh38.p7 | 14:31167151 | CACTCCAACTTGGGT[A/G]ACAGAGCAAGACCTG | 25831 |
rs577329050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31138833 | GAAACTATTCCATGC[A/G]GTAGAATGCAGAACA | 25831 |
rs577399616 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120249 | ATTAGCTGGGCATAG[C/T]GGCAGGCGCCTGTAA | 25831 |
rs577410797 | snp | A/T | 3.32607e-05 | 0.0040779 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123078 | CACAACCTTATGTCA[A/T]CACAATTAAGAAAGC | 25831 |
rs577415349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31131634 | AAAACTGTTGTGCCA[C/T]TGTATCTTGGGAAAA | 25831 |
rs577415763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31185270 | TGTGAACCTAGGAGG[C/T]GAAGCTTGCAGTGAG | 25831 |
rs577429036 | in-del | -/A | 0.00056539 | 0.016804 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139862 | CTAGATGCATTCAGC[-/A]ATACTAGCTACTACA | 25831 |
rs577449796 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31145630 | GAGCCAAGATTGTGC[C/T]AGTGCCTGGGTGACA | 25831 |
rs577463867 | in-del | -/AA | 0.00358779 | 0.0422022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31196811 | TGGTAGAAAGTAAGG[-/AA]AGTACTTATTGATAC | 25831 |
rs577556098 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184948 | ACCTGAAAGTTCACA[C/T]TGAAACTAAAAAAAA | 25831 |
rs577672195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31137662 | GGAGGATCAGCTGAG[C/T]CTGGGACACGGAGAG | 25831 |
rs577727968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141768 | AGTTTCTTTTGTGTG[C/T]ATAAATGTTACACTA | 25831 |
rs577738213 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131375 | TTCAAATATATTTTA[C/T]AGATCAGTAACATTA | 25831 |
rs577739226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136231 | TATACATTTTTATGG[C/T]TATATGATACTCAAA | 25831 |
rs577757278 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECTD1 | GRCh38.p7 | 14:31191688 | CTTTCAAAAATCAAA[A/C]CCCAGCTTTCACTTA | 25831 |
rs577758090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101622 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 25831 |
rs577782674 | snp | A/G | 0.000183307 | 0.00957184 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107545 | GTCACAACTCAAGTC[A/G]CAAAATGAGAAATAT | 25831 |
rs577801114 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134401 | GCCTTAATTCTATAA[C/T]GAGCAATAGCCACTG | 25831 |
rs577847407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31126840 | ACCTGGCTAATTTTG[C/G]GGATGTAGGGGTGGT | 25831 |
rs577879425 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167320 | AGTACAATCTGGTCA[C/T]GGTGGCATACTTGTA | 25831 |
rs577955764 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206332 | GAACACCTAACTAAA[C/G]GTTCTGTTTTTTCCA | 25831 |
rs578050963 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181172 | TAAAAACTGTACATC[-/A]AAAAAAAAAATAAAA | 25831 |
rs578069049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31192984 | CCACCTCAAAAAAAA[A/C]TAAAGTAAGACATGC | 25831 |
rs578073820 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECTD1 | GRCh38.p7 | 14:31179461 | TAAAATAAAACAAAA[C/T]AAAATAAATAATAAT | 25831 |
rs578133536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31200170 | TCATATTTAATCATT[C/T]GACAAATCCTGACTA | 25831 |
rs578133839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31151354 | AGTGAATCAAATATA[C/T]TCATTCCCATGATCA | 25831 |
rs578144902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150457 | CCTCTAACTCCTGGC[C/T]TCAGGCAATCCTTCC | 25831 |
rs578145385 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208097 | CGCACGGCACAGCAC[A/G]GCAAAGCTGCGGCCC | 25831 |
rs578161222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164399 | AGCGATCCTACTACC[C/T]CAGCTTCCCAAGTAG | 25831 |
rs578162651 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31186132 | TCATCCATTCTCTTA[A/G]TTCATACACCACAAA | 25831 |
rs578218308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114503 | TATTTTTTGTAGAGA[G/T]AAGGTTTTGCTATGT | 25831 |
rs745311283 | in-del | -/A | 1.69578e-05 | 0.0029118 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116192 | GCTTCTTGGCTCTAC[-/A]ACTAGGACATTATCT | 25831 |
rs745313812 | snp | C/T | 1.66621e-05 | 0.00288631 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139846 | AAGTGTCACACTGTT[C/T]CTAGATGCATTCAGC | 25831 |
rs745347996 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198799 | ATGCCTGTAATCCAG[A/T]ACTTTGGGAGGCCAA | 25831 |
rs745361369 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153820 | CTCAATCTCAAAAAA[C/T]AAAACAAAAAAAGAA | 25831 |
rs745382492 | snp | A/G | 4.96964e-05 | 0.00498455 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101090 | AAGAAAGCAAACACA[A/G]CAGAAGACCATGAGT | 25831 |
rs745410653 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138499 | CATAATAAAAGGCAT[C/T]GGTGCACTGTCTTTG | 25831 |
rs745424751 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158594 | AACATGTAACCTGAT[-/C]TTTTAAAATAAAAAA | 25831 |
rs745429709 | snp | C/T | 1.65608e-05 | 0.00287752 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173322 | TCGTCCTTCAAATAA[C/T]AGCACCAAGAGAAGG | 25831 |
rs745459027 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152121 | GAAATCTGCAAAGTA[A/G]TTTCCACTGAGTACT | 25831 |
rs745517108 | snp | A/C | 1.65905e-05 | 0.0028801 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148899 | TCTACATACTTACCC[A/C]GGGAAGTTTCTGCAG | 25831 |
rs745527036 | in-del | -/ATT/ATTTAAAAT | 1.81602e-05 | 0.00301326 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128052 | ATAGGTGAGATTGTA[-/ATT/ATTTAAAAT]GAAACCTCAGAAAAA | 25831 |
rs745612420 | snp | C/T | 1.65875e-05 | 0.00287984 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148834 | ATTCACAGAGCTTAC[C/T]TTGTTACAATTTAAC | 25831 |
rs745616148 | in-del | -/AGAC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188143 | GATAGATAGATAGAT[-/AGAC]AGACAGATAAAAGCT | 25831 |
rs745624933 | in-del | -/GTCA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132095 | AACATGAAATTAAAT[-/GTCA]GTCATTCTCGTAAGT | 25831 |
rs745646352 | snp | G/T | 0.000137864 | 0.0083014 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106314 | ACATACCAACCAATT[G/T]TTGAGCTTTGCAAAG | 25831 |
rs745664377 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196124 | GTTCAAGCGATTCTC[A/G]TGCCTCAGCCTCCTG | 25831 |
rs745679492 | snp | A/G | 1.68306e-05 | 0.00290087 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168492 | AGACAAATATTTTTT[A/G]AAGAAATACTTTTTT | 25831 |
rs745699304 | snp | A/G | 1.65754e-05 | 0.00287879 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105548 | GGCCTTGCTAAGAGG[A/G]TATGTCAGAACTTAC | 25831 |
rs745716537 | snp | A/G | 0.000133563 | 0.00817089 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133494 | AGTTAGAAAAGCCTC[A/G]TATCATCTCTTTACC | 25831 |
rs745717980 | snp | A/G | 0.000215662 | 0.0103819 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175079 | GAAGGTAAGCACACA[A/G]TTCAAACCACCAGCC | 25831 |
rs745774847 | snp | A/G | 4.96044e-05 | 0.00497993 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144052 | CCACTCTACCGAAGG[A/G]GTAACTACAAATAAT | 25831 |
rs745794632 | snp | C/T | 1.65996e-05 | 0.00288089 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133373 | AACGTACTAGACGTC[C/T]CTGCCGTCTAAGATT | 25831 |
rs745824963 | snp | A/G | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100210 | AAATGTTTATAATAT[A/G]CAAAGAAAATACAAC | 25831 |
rs745843686 | snp | C/T | 1.68046e-05 | 0.00289862 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112570 | CAAATAATAATGTCT[C/T]AGTGCTATAAGGCAT | 25831 |
rs745863266 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176472 | CTAATATGGTAAATA[A/G]ATAGACAAAACCTAT | 25831 |
rs745901352 | snp | C/T | 1.65652e-05 | 0.0028779 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128921 | GAGAACTAACACTGA[C/T]AATTCCCATGGATAT | 25831 |
rs745905937 | snp | C/T | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150032 | CTTCCGGACTACCAC[C/T]TGAATACATGGTGGC | 25831 |
rs745938416 | snp | C/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168472 | GGACACATCCAATCA[C/T]CTACAGACAAATATT | 25831 |
rs745961330 | snp | A/G | 8.32286e-05 | 0.00645038 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31172100 | AGTCTGACCTACATC[A/G]TCCATAAAATTTACT | 25831 |
rs745967690 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31169726 | TCTCTACTAAAAATA[C/T]AAAATTAGCCGGGTG | 25831 |
rs746008215 | snp | C/T | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178205 | TGTCTGGAGCACTTT[C/T]ATCAAGAAAAATTTT | 25831 |
rs746015171 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120867 | TTGGAAAGAATTAGT[G/T]AATATACATAAAGTA | 25831 |
rs746020640 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181676 | CAAAAAGGTCAAAAC[C/G]CAGAAAGCTCTAACC | 25831 |
rs746054373 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147530 | GGAAGGCTAAGGAGG[A/G]TGGATCACCTGAGGT | 25831 |
rs746054427 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132144 | CTAGCTCTTTAAATA[C/T]GTGGTGTAAGTTGCC | 25831 |
rs746060517 | snp | A/G | 0.000132477 | 0.00813761 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135054 | AAACCAGGCATTCTT[A/G]TCATCATTGCTATGA | 25831 |
rs746085613 | snp | A/G | 3.34778e-05 | 0.00409119 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171982 | ATGATAACGAATCAT[A/G]AAGCTGCTTTTTATT | 25831 |
rs746112864 | snp | C/T | 1.66222e-05 | 0.00288285 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178023 | AGTAATACTTACCTT[C/T]ACACACTGTTCGGCT | 25831 |
rs746177248 | snp | C/T | 3.31241e-05 | 0.00406952 | missense | HECTD1 | GRCh38.p7 | 14:31113369 | CCACAAGAGTTCTGT[C/T]CATTGCCTGCTTTGG | 25831 |
rs746183480 | snp | A/G | 3.31802e-05 | 0.00407296 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134901 | ACTGCAGTCATCAAC[A/G]TGGGTATACAAAGAA | 25831 |
rs746183961 | snp | A/G | 1.68349e-05 | 0.00290123 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144906 | TTCAACAGCTTTAAA[A/G]TGGTCATCGTATAAA | 25831 |
rs746251594 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193746 | CTGGCCAACATGGTA[A/C]AATCCTGTTCCTACT | 25831 |
rs746254847 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183710 | TAGTAAAATTTTGTC[-/T]TTTTTTTTTTTTTTT | 25831 |
rs746265405 | in-del | -/G | 1.7479e-05 | 0.00295621 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172135 | GGCTGAAATTTTGAA[-/G]GGAAAAAAAAAGAAA | 25831 |
rs746293283 | snp | A/G | 3.31538e-05 | 0.00407134 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121453 | GTAACAGCATGATGC[A/G]TTACATCAGAGCGGG | 25831 |
rs746295317 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142284 | AACAGTACTATTTAC[G/T]TTAATAAGTATTAGG | 25831 |
rs746308300 | in-del | -/C | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119542 | GCTCCTTTAAAAAAA[-/C]CTTTACTTTTTAAAG | 25831 |
rs746329882 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124604 | TCAAGATGGGAACAG[C/T]AGACACTAGCGACTC | 25831 |
rs746344166 | snp | A/T | 1.65605e-05 | 0.0028775 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129311 | ATTGCGTTGTGCCTG[A/T]AACAGTGGATGAAAC | 25831 |
rs746346293 | snp | G/T | 3.32674e-05 | 0.0040783 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121360 | TATACATATGGTAGG[G/T]AAGATAAACATGAAG | 25831 |
rs746348607 | snp | G/T | 1.66416e-05 | 0.00288453 | intron-variant | HECTD1 | GRCh38.p7 | 14:31102905 | TGATCTTGGAAAATA[G/T]TATCACATACCTGTC | 25831 |
rs746349907 | snp | A/T | 1.73721e-05 | 0.00294716 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157046 | ATAAGTTTAGTTGCC[A/T]GGAGTAGAGAAATGC | 25831 |
rs746376129 | snp | A/G | 1.65751e-05 | 0.00287876 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101261 | AGTGGTAAACTGCAA[A/G]AATGCTTTCCTTTCA | 25831 |
rs746383119 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125485 | GCCAGTTCACTCTTT[C/G]CTACCCACAATCATC | 25831 |
rs746390486 | snp | A/G | 1.6713e-05 | 0.00289072 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173461 | AAAGATGTTTAATAT[A/G]TTAGCATTATACAAA | 25831 |
rs746426579 | in-del | -/AT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176401 | CCTGTTATGTATAAC[-/AT]GTAATTAATTTATTT | 25831 |
rs746442003 | snp | A/G | 0.000255895 | 0.0113085 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129498 | AAAGCAGATAGGAGC[A/G]TGTCAGACAGTAGCT | 25831 |
rs746489322 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31173059 | AAGGGGTGCCACTTT[A/G]TTATCTGGATTTCTA | 25831 |
rs746527449 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161723 | AGGAGTTCGAGACCA[A/G]CCCAGCCAACATGGC | 25831 |
rs746552824 | in-del | -/TTT | 1.6566e-05 | 0.00287797 | cds-indel, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128871 | TTGTGAAGCTGCTTC[-/TTT]ATTAGTTAATTCAGA | 25831 |
rs746561256 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115513 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 25831 |
rs746561652 | snp | C/T | 1.66394e-05 | 0.00288434 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101309 | TAAAACCCTCACAAA[C/T]CTCAGGAAACCAGGG | 25831 |
rs746567270 | snp | G/T | 4.97096e-05 | 0.00498521 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31109528 | CTCCAGGGTCATCTC[G/T]CCTAACACTGCTTGT | 25831 |
rs746570962 | snp | C/G | 1.66771e-05 | 0.00288761 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173601 | TGATTACTCAATTTG[C/G]AATCTGCAGTGGTGG | 25831 |
rs746588888 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103458 | GAGGCAGGAGAATGG[C/T]GTGAATCCAGGAGGC | 25831 |
rs746594041 | snp | A/T | 1.65616e-05 | 0.00287759 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129339 | AACAGGTTTGGGTGA[A/T]GCCACTGTATCAGGG | 25831 |
rs746621332 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155174 | ATATGATGAAACCCT[A/G]TCTCTACTAAAAATT | 25831 |
rs746637727 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139861 | CCTAGATGCATTCAG[A/C]AATACTAGCTACTAC | 25831 |
rs746653088 | snp | A/G | 1.66092e-05 | 0.00288172 | missense | HECTD1 | GRCh38.p7 | 14:31106980 | ACTGACTTTCAGTAC[A/G]GTGTAAGTCTCTATC | 25831 |
rs746659061 | snp | C/T | 0.000184068 | 0.00959167 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173471 | AATATATTAGCATTA[C/T]ACAAAAACACTTTTT | 25831 |
rs746660678 | snp | C/T | 1.66123e-05 | 0.00288199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109372 | GTCATTCCTGTTCCC[C/T]AAATCTAATTTTATA | 25831 |
rs746677811 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139518 | GAGCAATGAATTTCT[A/G]TTTATTAAGTTCGCA | 25831 |
rs746688133 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124698 | GAGTGATAAGATCAA[C/T]AGAAGTCCAAATCTC | 25831 |
rs746711648 | snp | C/T | 3.31494e-05 | 0.00407107 | missense | HECTD1 | GRCh38.p7 | 14:31116257 | GTGGGCTCCCAAATA[C/T]GCCTAAGTTTATCTG | 25831 |
rs746714025 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187986 | GTCTCAAACTCCAGA[C/T]CTCAGGTGATCTGCC | 25831 |
rs746731949 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198067 | CTGTACTAGATAACT[A/G]TATTCTTCACTGCCA | 25831 |
rs746760929 | in-del | -/CTT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126600 | GTTCTTCCATTAAAA[-/CTT]CTTTTGTGACAAAAT | 25831 |
rs746766119 | snp | C/T | 3.33433e-05 | 0.00408296 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149096 | CAGTATAGGTTGACT[C/T]GAAGTAGATGGCTTT | 25831 |
rs746848788 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31128277 | TCTAAACAAAAGCTA[C/T]ACTTATATGATGCTT | 25831 |
rs746854990 | snp | C/T | 1.65745e-05 | 0.00287871 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127974 | CAGGTGTGGTCAAAT[C/T]AGGGAAACTCTGAGC | 25831 |
rs746892071 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130418 | GATATTCAATCTATA[C/T]ATTTACTTGTAGTAG | 25831 |
rs746893081 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165776 | CATAAGACCAGCTCT[C/T]GTGGTGCTTACTTTA | 25831 |
rs746905160 | in-del | -/GTGTGTG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134520 | TGTGTATGCATAAAT[-/GTGTGTG]TGTGTGTGTGTGTGT | 25831 |
rs746908479 | snp | G/T | 0.000150516 | 0.00867382 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133711 | AAATTATGTAATATT[G/T]TAAAAGATGAAAAAG | 25831 |
rs746938158 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101376 | GCAGATTTAAATGAA[A/G]ATCACTACCACTATT | 25831 |
rs746954972 | in-del | -/AGT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188362 | TGCCTCAGCCTCCCA[-/AGT]AGCTAGGATTACAGG | 25831 |
rs746957552 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117698 | CCAATTTTTTGAAAA[C/T]ATAAATACTTCTACA | 25831 |
rs746991269 | snp | A/C | 1.66021e-05 | 0.0028811 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175093 | AATTCAAACCACCAG[A/C]CTCAAAGACTGCTCC | 25831 |
rs747046399 | snp | A/G | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119775 | GGTCTAGGATCAAAA[A/G]CAGGAACCAATGCAG | 25831 |
rs747048262 | in-del | -/A | 0.000972518 | 0.0220298 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173137 | TTTCTTTTTATATTT[-/A]AAAAAAATATTTTCT | 25831 |
rs747060392 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202090 | AGGAGATTGAGACCA[C/T]CCTGGCTAACACAGT | 25831 |
rs747061091 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203432 | TCTTGTATCTTCATA[G/T]AGTAAATCATATCTG | 25831 |
rs747094522 | snp | C/T | 3.31505e-05 | 0.00407113 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150217 | TCTTCCTGTGGTTCA[C/T]CTTCCTAAATGTGTA | 25831 |
rs747115706 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190245 | CAGAGACAAGCCATC[C/T]CCACTCTACCCTTTC | 25831 |
rs747136944 | snp | G/T | 1.66051e-05 | 0.00288137 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173181 | AATTGCATCTATAAG[G/T]GCATCGGTATCTTTA | 25831 |
rs747139190 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141642 | TAAGTGATCAGCTGC[A/C]TTCATACCAGACATG | 25831 |
rs747139232 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158176 | ATTAGTATGCCTCCT[G/T]TCCCTTTTATTCACT | 25831 |
rs747147743 | snp | A/G | 4.96849e-05 | 0.00498397 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129030 | TGTTAAGGTGCTGGT[A/G]CTTGCACTGGAAGAT | 25831 |
rs747181232 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110212 | TCTGCCATGTTGCCC[A/T]GGCTGGTCTTGAATT | 25831 |
rs747198928 | snp | C/T | 9.93772e-05 | 0.00704831 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128946 | GGATATTGCACTAGA[C/T]TCCCCAGGAGTACGA | 25831 |
rs747220631 | snp | A/G | 1.66499e-05 | 0.00288525 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205772 | TACAGTAACCCAAAG[A/G]AACATGATGAAGGAA | 25831 |
rs747224930 | snp | A/G | 1.65641e-05 | 0.00287781 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150062 | CAAGTTTTCCATCCA[A/G]GATAAATCTGAACCA | 25831 |
rs747236028 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122204 | GGCTGGAAAGCAGTG[A/G]TGCAATTATAGCTAA | 25831 |
rs747245700 | snp | A/T | 1.66225e-05 | 0.00288287 | missense | HECTD1 | GRCh38.p7 | 14:31107141 | CCAAGGAAATGAAAC[A/T]GTTTCGTGATCCTTT | 25831 |
rs747299830 | snp | A/G | 3.39495e-05 | 0.0041199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172125 | TTTACTTCAAAGGCT[A/G]AAATTTTGAAGGAAA | 25831 |
rs747302677 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202199 | AGCGAGACTCTGCCT[-/C]AAAAAAAAAAAAAAA | 25831 |
rs747321678 | snp | A/C | 1.84831e-05 | 0.00303993 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135455 | TGGTCACTCCAGCTT[A/C]AAGTAAAATGACTGA | 25831 |
rs747343705 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194969 | AGATATTTTATAAAA[C/T]AGTCTGTAAATCAGG | 25831 |
rs747363620 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183665 | TTTGTGTCATCACTA[C/T]TCAACTTAAAACTTA | 25831 |
rs747366777 | in-del | -/TAAT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176404 | GTTATGTATAACATG[-/TAAT]TAATTTATTTTAAGA | 25831 |
rs747375907 | snp | A/T | 3.31417e-05 | 0.00407059 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148967 | AAAACCAGGTAAATC[A/T]TCTTTCAATATTGTA | 25831 |
rs747376160 | snp | A/C | 1.66117e-05 | 0.00288194 | missense | HECTD1 | GRCh38.p7 | 14:31106966 | TGTAGAAGCTTCAGA[A/C]TGACTTTCAGTACAG | 25831 |
rs747387638 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147684 | AATAGCCTGAACCCA[A/G]GAGGCAGAGGTTACA | 25831 |
rs747413892 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133882 | AACATTTAAATGTAC[A/G]CTATTGATTTGACTC | 25831 |
rs747429668 | snp | C/T | 3.36774e-05 | 0.00410336 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113525 | CCATTAATCACATTT[C/T]CAAGAAAAACAGTGT | 25831 |
rs747454781 | snp | A/G | 3.39069e-05 | 0.00411732 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144915 | TTTAAAATGGTCATC[A/G]TATAAATCTCGAGCC | 25831 |
rs747460659 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167728 | ATACTGTTCTTCACT[C/T]ATGCTTCCAAATCTG | 25831 |
rs747487339 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163194 | TTGGGAGGCTGACGT[C/T]GGAAGATCGCTTGAG | 25831 |
rs747503703 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165016 | AAAAAAAAAAAAAAA[-/G]TGACCCCACTAACAC | 25831 |
rs747504860 | snp | G/T | 1.65611e-05 | 0.00287755 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122898 | CTTTGTAAAGAGAAT[G/T]GGGTACTCTCTCTAC | 25831 |
rs747508509 | snp | A/G | 1.65677e-05 | 0.00287812 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157260 | TTAACAGTGCTTCAG[A/G]GCAAAAATGAATCAT | 25831 |
rs747527975 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126705 | ATATTTTTTCAGAGA[G/T]AGGGTCTAGCCCTGT | 25831 |
rs747534443 | snp | G/T | 1.65625e-05 | 0.00287766 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168300 | TATGAATAACTACCT[G/T]ATTGAAGGCAGCATA | 25831 |
rs747542032 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102652 | CCAGGCTGGTCTCAA[A/T]CTCCTGACCTCAAGT | 25831 |
rs747561989 | snp | C/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208229 | CGCTCCTGGGAGGCC[C/G]ACCGCCTGGCGGTTC | 25831 |
rs747577719 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208062 | GTGGCTAACACTTTG[C/T]GCGCTCCTGCGGAGG | 25831 |
rs747610846 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175733 | GCCGGGCATGGTGGC[A/G]CATGCCTCTAATCCC | 25831 |
rs747619516 | snp | A/C | 5.12711e-05 | 0.0050629 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148704 | AGACAAGAATAAAGC[A/C]CATCCAACAGATATA | 25831 |
rs747683774 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115533 | GGAGGCTGAGGTGGA[C/T]GGATCACTTGAGCTC | 25831 |
rs747697249 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209446 | AATTATGGAAAGTGT[C/T]TAGAACGACTAAAAG | 25831 |
rs747706986 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147829 | TTATTACAATTTCTC[C/T]GGTCAAAGCCATAAA | 25831 |
rs747707075 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164588 | ATAACTATCCTCACC[C/T]TGGAGACGAGCCAAT | 25831 |
rs747746958 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125660 | ATTTTGCTACACACA[C/T]GTTTAATAAGCAGAA | 25831 |
rs747748452 | snp | A/G | 1.65608e-05 | 0.00287752 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122915 | GGTACTCTCTCTACC[A/G]TAACCTCCTCGTATT | 25831 |
rs747779930 | snp | A/G | 3.336e-05 | 0.00408398 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173613 | TTGGAATCTGCAGTG[A/G]TGGATGGAGCTCCTG | 25831 |
rs747782936 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174689 | ACATTTTTATGATAT[C/T]TAAATTTTAAGAATA | 25831 |
rs747796756 | snp | C/T | 6.63625e-05 | 0.00575993 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157285 | AATCATTTTTCGAAT[C/T]AGAGCAAGACTTGCT | 25831 |
rs747841617 | in-del | -/A | 1.68736e-05 | 0.00290457 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106636 | GAAGAATGTACATAT[-/A]AATGCTTACCCTAAA | 25831 |
rs747848561 | snp | A/T | 0.000170123 | 0.00922131 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112398 | TTATTCTAAAAACAT[A/T]AAAAAAAGGCTTCTT | 25831 |
rs747869946 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188195 | TCTGTCTAAAATCCT[C/T]TTCCCCTAACTCTTT | 25831 |
rs747892086 | snp | C/G | 1.75133e-05 | 0.00295911 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140042 | TTTGTATAACTACAT[C/G]TAAATGTTCATGCAG | 25831 |
rs747925611 | in-del | -/TT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183194 | ATAAATTATATAGAA[-/TT]TGTTATATTTTATTT | 25831 |
rs747934276 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143989 | AAGAAATTAGAAATA[A/T]TAACATCATTCAGCT | 25831 |
rs747943699 | snp | A/G | 4.97211e-05 | 0.00498579 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139917 | TATGTGGATCCTGGT[A/G]TATCATACAAATGGA | 25831 |
rs747945003 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152756 | TAAAGAGGCCAGGTG[C/T]GGTGGATCACTTTGA | 25831 |
rs748010306 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189312 | CCTTAGAATTCCAAC[C/G]CTCCTCACTTCTTTT | 25831 |
rs748014798 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156691 | TGTTGATCAAAATGT[C/T]TTAAAAGAAAATTGA | 25831 |
rs748016010 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154808 | CTCGGGATTCTACAA[C/T]TATTAACTCATATAC | 25831 |
rs748020228 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108589 | AGCACTTTGGGAGGC[C/T]GAAACGGGTGGATCA | 25831 |
rs748023669 | snp | C/T | 1.67161e-05 | 0.00289098 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172027 | TAATTTAAATACCAG[C/T]TTTTATTTATTAGCT | 25831 |
rs748071299 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31119148 | CTTGTGATTACACTG[C/T]GTCCACTTGGATGAT | 25831 |
rs748072436 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108477 | TAAAGTGATTGCATA[A/T]AGTATAATAAAAACT | 25831 |
rs748102440 | snp | C/T | 1.68139e-05 | 0.00289943 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149111 | TGAAGTAGATGGCTT[C/T]ACTTGGCCTCGAGCT | 25831 |
rs748105969 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120579 | GTTGGTTTTTAAAAC[A/G]TAAATTACATTTTGT | 25831 |
rs748122259 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31107537 | AAAGCAGAGTCACAA[C/T]TCAAGTCACAAAATG | 25831 |
rs748122375 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181100 | ATCAAATGACAAGAA[C/T]AGATTTACCATATGC | 25831 |
rs748124591 | snp | A/G | 1.65685e-05 | 0.00287819 | missense | HECTD1 | GRCh38.p7 | 14:31116278 | AGTTTATCTGATTTC[A/G]CATTGCCATTACAGG | 25831 |
rs748147935 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198980 | GGTGGAGGTTGCAGT[A/G]AGCCAAGATCGCACC | 25831 |
rs748157493 | snp | C/G | 1.66804e-05 | 0.00288789 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171944 | CATCTGCACCTCTCT[C/G]ACAAAGAAATTCTAC | 25831 |
rs748161013 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143244 | CATGACAAAACCTCG[C/T]CTCTACTAAAAATAC | 25831 |
rs748179357 | snp | G/T | 0.000139344 | 0.0083458 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144098 | TTTGTTCTTTACTAC[G/T]TGATAAACTTACATT | 25831 |
rs748187834 | snp | C/T | 1.66043e-05 | 0.00288129 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133529 | TGATCTTCACATACT[C/T]CATTTACAGTGCCAT | 25831 |
rs748208690 | snp | A/T | 2.06772e-05 | 0.0032153 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144270 | ACACTAAAAGAAAAA[A/T]AAATTTAATGAAGGC | 25831 |
rs748217626 | snp | A/C/T | 5.65769e-05 | 0.00531844 | missense | HECTD1 | GRCh38.p7 | 14:31113186 | TGAAGCTGTTCATCA[A/C/T]CATCTATAAAATTAA | 25831 |
rs748220289 | snp | A/C | 1.65748e-05 | 0.00287874 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31174952 | TAGACAGAGATTCTA[A/C]ACAAATTTCTAAAGA | 25831 |
rs748227440 | in-del | -/ATGAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104331 | AAATACCCATTACCG[-/ATGAA]ATGGACAGAAGATGA | 25831 |
rs748245125 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137753 | TTGAAAAGAAAAAAA[-/G]AAAAAAAAGAAAACA | 25831 |
rs748262676 | snp | A/G | 3.32806e-05 | 0.00407912 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31174925 | CCTGATGATCTTCAT[A/G]CTTTAATAAACTAGA | 25831 |
rs748267508 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192490 | AAGCTGGTTCTTGGA[A/G]AAGGTTCTTGGACAA | 25831 |
rs748272783 | snp | G/T | 1.66056e-05 | 0.00288141 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119912 | AATAAGATGCAAAAT[G/T]TCATTGTTGCAAAAG | 25831 |
rs748274538 | snp | C/T | 3.39801e-05 | 0.00412176 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112589 | GCTATAAGGCATTCA[C/T]GCATGCATGCATTCA | 25831 |
rs748298708 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144728 | GACCCCCTACTCAAT[A/G]CCCATGACATAAAGG | 25831 |
rs748303684 | snp | C/T | 1.84025e-05 | 0.0030333 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156819 | ACTCTTCCTGATACC[C/T]CTATAATTAAGACCA | 25831 |
rs748340139 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110455 | GAATCAATTTCCTCA[C/T]TTATAAAACAAATTA | 25831 |
rs748381893 | snp | C/T | 1.65666e-05 | 0.00287802 | missense | HECTD1 | GRCh38.p7 | 14:31101064 | TTGCATCAGTAGCAT[C/T]AACCTACAACAAGAA | 25831 |
rs748395167 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111479 | GGATGGTCTCGATCT[C/G]CTAACCTCATGATCT | 25831 |
rs748441693 | snp | G/T | 4.98641e-05 | 0.00499295 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150237 | CTAAATGTGTAGAAT[G/T]ATTCAATTAAACATG | 25831 |
rs748447544 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203644 | AATAAAGCCTAGAAA[A/G]GAAAATGGAAAAAAT | 25831 |
rs748457639 | in-del | -/GTT | 1.65611e-05 | 0.00287755 | cds-indel, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129270 | TGTCTTGTCTGGACA[-/GTT]GTTTTTCACCAAGCT | 25831 |
rs748470957 | in-del | -/GGTG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134564 | GTGTGTGTGTGTGTG[-/GGTG]TGTGCGCGCGTATGT | 25831 |
rs748506823 | snp | A/C | 1.68131e-05 | 0.00289935 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100885 | ACACAAGAGGCTTCA[A/C]TAGTATTTTTAAAGT | 25831 |
rs748508919 | snp | A/G | 2.27239e-05 | 0.00337067 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107293 | AAATAAAATTAAACA[A/G]AAGTTAATAGAAACT | 25831 |
rs748524391 | snp | A/G/T | 0.0001325 | 0.00813841 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128960 | ACTCCCCAGGAGTAC[A/G/T]AACAGAACTATCAGG | 25831 |
rs748533157 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202341 | GCTATCACACAACTA[C/T]TCAGTGGAAAAGGCA | 25831 |
rs748563826 | snp | C/T | 3.32602e-05 | 0.00407786 | missense | HECTD1 | GRCh38.p7 | 14:31107153 | AACAGTTTCGTGATC[C/T]TTTCAAGCTCATCAC | 25831 |
rs748577837 | snp | A/C/T | 3.58392e-05 | 0.00423303 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135470 | AAAGTAAAATGACTG[A/C/T]CTTACTTTGCATTTG | 25831 |
rs748615529 | snp | C/G | 1.65743e-05 | 0.00287869 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135664 | TAATAATGCTGTTTT[C/G]AAGCACGTTACCTAC | 25831 |
rs748617465 | in-del | -/AACATA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193083 | AAGTAAAAACCTTCG[-/AACATA]AACATAAAAATTTAT | 25831 |
rs748621404 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149359 | GAGATGATCACTTGA[A/G]CTCACGAGTTTGAGG | 25831 |
rs748622523 | snp | C/G | 3.31625e-05 | 0.00407188 | synonymous-codon, intron-variant | HECTD1 | GRCh38.p7 | 14:31113955 | TAATTTCCAGTGGCG[C/G]AGGAAAGCAGCGTCT | 25831 |
rs748653003 | snp | A/C | 1.65723e-05 | 0.00287852 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205803 | TGTACTTACGTTTCA[A/C]AACAACGATCCACGT | 25831 |
rs748670785 | snp | A/G | 3.31835e-05 | 0.00407316 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116238 | TAAAATTTCTTACGT[A/G]TATGTGGGCTCCCAA | 25831 |
rs748693128 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117715 | TAAATACTTCTACAG[C/T]CACCTATGTGTACAA | 25831 |
rs748702385 | snp | C/T | 1.65949e-05 | 0.00288048 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148886 | ATAAACTTACATATC[C/T]ACATACTTACCCAGG | 25831 |
rs748708102 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183845 | CCCAAGTAGCTGGGA[C/G]CACAGGCATGCACCA | 25831 |
rs748728984 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195904 | CCTATGGACCCCCTG[C/G]AGTCCCAGGTAAACC | 25831 |
rs748730554 | snp | C/T | 2.39066e-05 | 0.00345727 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114270 | AAGAGTAAACCAATG[C/T]TCTAAAATAACTTAC | 25831 |
rs748733276 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165641 | TGTACTCCATTAATA[C/T]TGAAATACTTGCAAC | 25831 |
rs748782202 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185198 | ATACAAAAAATTAGC[C/T]GGGTGTGGTGGCAGG | 25831 |
rs748810926 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132814 | ACTAACAGATAAAGA[C/G]ACAATGTTTCTTGTT | 25831 |
rs748844795 | snp | A/G | 3.31658e-05 | 0.00407208 | synonymous-codon, intron-variant | HECTD1 | GRCh38.p7 | 14:31113973 | GAAAGCAGCGTCTGC[A/G]TTCTTCTGCAGGTAG | 25831 |
rs748855126 | snp | A/G | 1.65674e-05 | 0.00287809 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127819 | TTCCTGACCTGTGTC[A/G]CTCTCACTGGAAGTT | 25831 |
rs748859378 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104286 | TCAAAATGCCCCATA[A/C]ACATGTACATATATT | 25831 |
rs748860996 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197102 | GAAGTAGTGTATACA[C/T]GTGAGAATATGCAGG | 25831 |
rs748889629 | in-del | -/TA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125746 | TGAATTAGGAGAGGC[-/TA]TATTCTCACAAAAAG | 25831 |
rs748924239 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31128436 | TCACACCTAGTCTGA[A/T]TTCTGCAAATATTAT | 25831 |
rs748933537 | snp | A/G | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168367 | CTTTTCAAGTATATG[A/G]GTGCCATTTCCGGAT | 25831 |
rs748958973 | snp | A/C | 1.66579e-05 | 0.00288595 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168476 | ACATCCAATCACCTA[A/C]AGACAAATATTTTTT | 25831 |
rs748962126 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153369 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 25831 |
rs748963603 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189942 | TAGTGAAAGTGACCA[C/G]TGTGTGACTTCAAAT | 25831 |
rs748971668 | snp | C/G | 1.66029e-05 | 0.00288117 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123061 | ATCTTGAAAACAAAA[C/G]CCACAACCTTATGTC | 25831 |
rs748980402 | snp | C/T | 1.65927e-05 | 0.00288029 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133364 | GAACCTGGGAACGTA[C/T]TAGACGTCTCTGCCG | 25831 |
rs748997396 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105150 | GGGATTACAGGTATG[C/T]GCCACCATGCCCAGC | 25831 |
rs748999862 | snp | A/G | 1.83775e-05 | 0.00303124 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174877 | AAAAAATCACTTTCT[A/G]AAAATGGAAAGTATG | 25831 |
rs749025485 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141438 | GTAATTTAAACTAAG[C/T]GATCAGGCTAGGAAC | 25831 |
rs749065040 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104577 | TTCTCATTTTCAAAA[A/G]TAATTTACCTTGTAA | 25831 |
rs749079726 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127309 | TCTCTCGTATTACTG[A/G]GTTTTTTCATATTAT | 25831 |
rs749085670 | snp | C/T | 1.799e-05 | 0.00299911 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173746 | ATGGAGCTGGGTCAA[C/T]ACCACGACGGGTAAA | 25831 |
rs749094128 | snp | C/G | 3.32535e-05 | 0.00407746 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105338 | TAATTTCAACTGTCT[C/G]AAAGTGAAAGGAGAG | 25831 |
rs749107980 | snp | G/T | 2.27684e-05 | 0.00337397 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141934 | GACTACAATCTTGTT[G/T]CATATCCAAATCCAT | 25831 |
rs749120156 | in-del | -/AA | 1.76993e-05 | 0.00297478 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114100 | GCCTTTCCCAATTAT[-/AA]AGTCTATGATATTTC | 25831 |
rs749145586 | snp | C/T | 9.97423e-05 | 0.00706125 | missense | HECTD1 | GRCh38.p7 | 14:31112423 | CTTCTTACCTTGAGG[C/T]GCCAAATGCTGTACA | 25831 |
rs749150360 | snp | C/G/T | 6.79791e-05 | 0.00582971 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133240 | AGCACCTACTCACCA[C/G/T]TGTGTAGTTCTCCTG | 25831 |
rs749171723 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156837 | ATAATTAAGACCACT[C/T]ACTTTTTCTGGTTTT | 25831 |
rs749176246 | in-del | -/TATT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148564 | TTATATGTAAATAAA[-/TATT]TAAGAAAACACAGAA | 25831 |
rs749203298 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31109968 | TTTCAAACTGAAAGC[C/T]GCCATCAAAACGGTA | 25831 |
rs749214921 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108770 | TTCTAGAGATGTATC[A/T]TATTTCTTGCAATTA | 25831 |
rs749220516 | snp | C/T | 1.65649e-05 | 0.00287788 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150207 | TTCTTTAGCATCTTC[C/T]TGTGGTTCATCTTCC | 25831 |
rs749227261 | snp | A/G | 3.85008e-05 | 0.00438736 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141827 | GTGTGAACATTACAA[A/G]CATCAAATTCAAAGA | 25831 |
rs749246052 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201663 | TACAGGCACATGCCA[C/T]AGTGCTCAGCTAAAT | 25831 |
rs749259517 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205658 | GGAAAAGTGTAAACA[A/C]AAAACTCTTCAGGAA | 25831 |
rs749271615 | snp | C/T | 1.73785e-05 | 0.0029477 | missense | HECTD1 | GRCh38.p7 | 14:31109572 | TCCACAGTGGCTTCA[C/T]GTCGGTTCTGTAACC | 25831 |
rs749280170 | snp | A/G | 1.73664e-05 | 0.00294667 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116496 | AAAAACAATTATACT[A/G]AAACAAGCAGTCCAA | 25831 |
rs749319102 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102334 | TATAAACGTAGTATA[C/T]AGCCCAACAGCTTAC | 25831 |
rs749325081 | snp | A/G | 1.67885e-05 | 0.00289724 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128012 | AGAGGAGAAGCTAAA[A/G]ACAAAAATGAAGCAA | 25831 |
rs749331678 | snp | C/T | 1.656e-05 | 0.00287745 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135017 | ATGCTGATGGTATCA[C/T]CCAGAGACCCAGATC | 25831 |
rs749351814 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193564 | GTCCTTTGCATTTCC[A/G]TATAAATTTTGAAAT | 25831 |
rs749351905 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179650 | TTGAGATATCATTAA[C/T]ACTCCCTATATTTTA | 25831 |
rs749354360 | snp | C/T | 1.65776e-05 | 0.00287898 | missense | HECTD1 | GRCh38.p7 | 14:31106746 | CAGAAAGACCTTTGT[C/T]GCTTAAAATTTGGCG | 25831 |
rs749365908 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31113359 | ATCTTCTACTCCACA[A/G]GAGTTCTGTCCATTG | 25831 |
rs749367146 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198439 | ATAACACTCAACTTT[A/G]CAAGCAAAAATGACA | 25831 |
rs749398660 | snp | C/G | 5.20793e-05 | 0.00510264 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134859 | TCCAATTTGCAAAGA[C/G]TCCTCAACTAACCCT | 25831 |
rs749405971 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167238 | GGGAGGCTGAGGTGG[A/G]CGATCACTTGAGCCC | 25831 |
rs749426992 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145057 | GGTACGTATGTACTG[A/T]CATTTGGGCACAAAT | 25831 |
rs749429523 | snp | C/T | 3.35537e-05 | 0.00409582 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178010 | TAATGAGCCAATAAG[C/T]AATACTTACCTTTAC | 25831 |
rs749435409 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112702 | GCAGCCTCTGCCTCC[C/T]GGGTTCAAGCGATTC | 25831 |
rs749449620 | snp | A/G | 0.000259218 | 0.0113817 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144284 | AAAAATTTAATGAAG[A/G]CAATCAAAAACATAA | 25831 |
rs749470780 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161316 | AGGCATAGTGGCTCA[C/T]GCCTGTAATCCCGCA | 25831 |
rs749472524 | in-del | -/CACACACA | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163095 | ACACACACACACACG[-/CACACACA]CACACATGCGCACAC | 25831 |
rs749482382 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130552 | GTTATAAGCTAACTA[C/T]TTCAGGGAAAAACAT | 25831 |
rs749490629 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101509 | ACTTTAAAAATATCC[C/T]GGGCCAGGTGTGGTG | 25831 |
rs749517473 | snp | C/T | 1.70067e-05 | 0.002916 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175142 | CAGTTCTAATACCTA[C/T]AATAGTAAAACAAAT | 25831 |
rs749535042 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146029 | ATTGAGACAATGTCC[G/T]CACTGATTTTTTTTA | 25831 |
rs749582753 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192697 | AGACATTCTACTGGC[C/T]GAGCGTGGTGGTTCA | 25831 |
rs749604453 | in-del | -/G | 3.3154e-05 | 0.00407135 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148814 | TGGGGGGAAAAAAAA[-/G]GAATATTCACAGAGC | 25831 |
rs749619901 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204859 | TCAATAATCAAAAAT[G/T]AAGGTACTTTAAAAA | 25831 |
rs749646054 | in-del | -/A | 0.00949659 | 0.0682503 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141980 | AAAAGTATAAAGTCC[-/A]AAAAAAAATAATTTA | 25831 |
rs749646823 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171441 | GGAATATTTTATTGA[C/T]GAATACAAACAAGAG | 25831 |
rs749656232 | snp | A/T | 1.65669e-05 | 0.00287805 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101225 | GTTAGCCAGTCCACC[A/T]GGGGGTAGAGTTGAA | 25831 |
rs749657935 | snp | A/C | 3.31307e-05 | 0.00406992 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101080 | AACCTACAACAAGAA[A/C]GCAAACACAACAGAA | 25831 |
rs749667220 | snp | C/T | 1.81431e-05 | 0.00301184 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156823 | TTCCTGATACCTCTA[C/T]AATTAAGACCACTCA | 25831 |
rs749701772 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160202 | AGTGAAGATACTGAG[C/T]GATAGTTAAGTCAGT | 25831 |
rs749709901 | snp | A/G | 1.6646e-05 | 0.00288491 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173437 | AGATCCTAGAAAGAG[A/G]ATGGGAAGAAAGATG | 25831 |
rs749715887 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111689 | ATGCAGGTACCTTTC[C/T]CTTTGGCTTCCTTCT | 25831 |
rs749728442 | snp | C/T | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173294 | ATCCAGCACTAGACT[C/T]TGGCAAAGCTTTTCG | 25831 |
rs749734821 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170779 | TGAGCACCTGCAATA[C/T]GCTGATTACTACAGT | 25831 |
rs749741104 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124390 | ACATGGTATAGTATT[C/T]GTGCCTGCGGTAAGA | 25831 |
rs749741848 | in-del | -/ATA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188117 | TAGATAGATAGATAG[-/ATA]GATAGATAGATAGAT | 25831 |
rs749752990 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108830 | AGTTGGATTCACCCC[-/T]GTGACAGGAGACGTA | 25831 |
rs749771651 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105351 | CTCAAAGTGAAAGGA[A/G]AGCAATTATGCTAAA | 25831 |
rs749778015 | in-del | -/AAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144265 | TCAATACACTAAAAG[-/AAA]AAAAAATTTAATGAA | 25831 |
rs749780540 | snp | C/G | 1.68142e-05 | 0.00289945 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31205981 | TGAAAAGTAAAGGGA[C/G]AAAAGTCCTTTAAAT | 25831 |
rs749782269 | snp | C/T | 1.65671e-05 | 0.00287807 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136665 | ATCTCCTTGTAAGTA[C/T]CTACACAAAAACGAT | 25831 |
rs749784511 | snp | C/G | 3.33684e-05 | 0.00408449 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107530 | ACTTTTGAAAGCAGA[C/G]TCACAACTCAAGTCA | 25831 |
rs749830973 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142979 | TACCAAAACTGAAAT[C/G]ATACAGAGAAGATTA | 25831 |
rs749831500 | in-del | -/TGCG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134567 | GTGTGTGTGTGTGTG[-/TGCG]CGCGTATGTATATAC | 25831 |
rs749904093 | snp | A/G | 1.65767e-05 | 0.00287891 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149054 | TGACCAATTTCCTAC[A/G]GTAAGTTTAGTGGGT | 25831 |
rs749934681 | snp | G/T | 1.65663e-05 | 0.002878 | missense | HECTD1 | GRCh38.p7 | 14:31116344 | GTTGATCTGAAATTG[G/T]TGAGTGGTAATTCAA | 25831 |
rs749936740 | snp | C/T | 3.36022e-05 | 0.00409877 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172006 | TTTTATTAATATTTC[C/T]ATCCTTAATTTAAAT | 25831 |
rs749947099 | snp | C/T | 1.68764e-05 | 0.00290481 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128612 | GAAAAGCTCACTTAC[C/T]TGCTGTGCTCATCAC | 25831 |
rs749980562 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199894 | TCTCAATCACATCCC[A/G]TGGCCACAATTAACC | 25831 |
rs749991471 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134519 | GTGTGTATGCATAAA[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 25831 |
rs749991931 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189506 | CAGTGGCTCACACCA[G/T]TAATCCCAGCACTTT | 25831 |
rs749993107 | snp | C/T | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119353 | ACTGACTCTAGAGGG[C/T]ATGACTGTAACCACT | 25831 |
rs749994186 | snp | C/T | 1.66239e-05 | 0.00288299 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31106822 | GTGTGGGTTTACTAA[C/T]TCAAAGTCTTCCCAA | 25831 |
rs750007953 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180860 | AGAGCTAGTCCAGCA[C/G]TTCTCAGGTAAGGTC | 25831 |
rs750020811 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131358 | GGTGCCATACCTCAC[A/G]GTTCAAATATATTTT | 25831 |
rs750043270 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101894 | CTATTCTGCAACAAA[A/G]TCAGCAAATCATAAA | 25831 |
rs750060583 | snp | A/T | 5.05267e-05 | 0.00502601 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171891 | TCTTCCAAAACATGC[A/T]GCATAATGTAATGAT | 25831 |
rs750066422 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188117 | TAGATAGATAGATAG[-/A]TAGATAGATAGATAG | 25831 |
rs750071526 | snp | A/G | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134967 | CCAATTTCTCAGTGC[A/G]GACCTTCCATAACCA | 25831 |
rs750076671 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146724 | CGGGCATGGTGGCGC[A/G]CACCTGTAATCCCAG | 25831 |
rs750093484 | snp | C/T | 1.65748e-05 | 0.00287874 | missense | HECTD1 | GRCh38.p7 | 14:31106688 | CCAGAACCTGATGGA[C/T]TCTTCAGCACTAGTT | 25831 |
rs750110892 | snp | A/G | 1.70909e-05 | 0.00292321 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177983 | ATCCCTGAGAGGTCT[A/G]AGAAAAATAAGTAAT | 25831 |
rs750119816 | snp | C/G | 3.31378e-05 | 0.00407036 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127962 | TTGATGTAGTACCAG[C/G]TGTGGTCAAATTAGG | 25831 |
rs750129660 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132888 | TCTATATGATTTATG[A/G]TACCATAAAAATTAT | 25831 |
rs750135625 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129323 | CTGAAACAGTGGATG[A/T]AACAGGTTTGGGTGA | 25831 |
rs750153385 | snp | C/T | 6.62438e-05 | 0.00575478 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205844 | CAAAAGCAGCATGCA[C/T]AGCTGTTCAAGGGCT | 25831 |
rs750171085 | snp | C/G/T | 0.000112329 | 0.00749361 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133702 | TTAGAGAAAAAATTA[C/G/T]GTAATATTTTAAAAG | 25831 |
rs750184737 | snp | A/C | 3.33411e-05 | 0.00408282 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144846 | AGATGACTCTAACTG[A/C]GTTGCTATGTTTCTG | 25831 |
rs750187391 | in-del | -/ACCAAAATAA | 0.00013892 | 0.00833312 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144944 | CCATAGTTCGTACCT[-/ACCAAAATAA]ACACAACAAATGTGA | 25831 |
rs750204022 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193175 | AATGAATTTCTCCTA[C/T]GTTTTCTTCTAGAAG | 25831 |
rs750226967 | in-del | -/TCAA | 1.65723e-05 | 0.00287852 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135663 | TTAATAATGCTGTTT[-/TCAA]GCACGTTACCTACTT | 25831 |
rs750281597 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166723 | TGGTGTGGTAGTGCA[C/T]GCCTGTAGTCCTAGA | 25831 |
rs750297689 | snp | G/T | 1.65888e-05 | 0.00287996 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157161 | TTTTGAAAAAGAAAC[G/T]GACCTCTTGATCCAG | 25831 |
rs750307709 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145708 | AAAATTATTTTTGCC[A/T]AAAATATTTTGATGC | 25831 |
rs750311327 | snp | A/C/G | 0.000161778 | 0.00899249 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144261 | ACTCTCAATACACTA[A/C/G]AAGAAAAAAAAATTT | 25831 |
rs750362570 | snp | C/T | 3.31807e-05 | 0.00407299 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156969 | TTTATCTACTAAATC[C/T]CTTATGATCTGCAAA | 25831 |
rs750385409 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160883 | ACTAGTTGCCCAGGC[A/T]GGTCTCAAACTCCTG | 25831 |
rs750386576 | snp | C/G | 1.65616e-05 | 0.00287759 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129261 | AGCAGCAGATGTCTT[C/G]TCTGGACAGTTGTTT | 25831 |
rs750414589 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103986 | AAAAACAAAAACAAC[A/G]AAGTTGATCTCATAA | 25831 |
rs750422718 | in-del | -/T | 1.97791e-05 | 0.0031447 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113094 | AGTTCAGCTGTCTGA[-/T]TTTTATTACCTCAAT | 25831 |
rs750435395 | snp | C/T | 1.65633e-05 | 0.00287774 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205898 | TCCCTGTCCCATCTG[C/T]AGCCATTCCAGCAAT | 25831 |
rs750437397 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195420 | GTACACTTACAAAGC[A/G]TTATAAAACACAATG | 25831 |
rs750443961 | snp | G/T | 1.65726e-05 | 0.00287855 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135607 | AAAATCATACCACTG[G/T]TTTGCTACCTAAACC | 25831 |
rs750459916 | snp | A/C | 1.71117e-05 | 0.00292499 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114075 | CTACAACAGGAAAAA[A/C]CAAATGTTGGCCTTT | 25831 |
rs750490155 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184688 | CAAGGCTGCAGTGAG[A/C]CATGATCACGCACAA | 25831 |
rs750491791 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159643 | CGCACCTGGCCATAA[-/T]TTTTTTTTTTTTTTT | 25831 |
rs750503446 | snp | C/T | 1.6615e-05 | 0.00288223 | missense | HECTD1 | GRCh38.p7 | 14:31107096 | AAGTCCACAAGTCTA[C/T]TGTCTTGAATGCATT | 25831 |
rs750518443 | snp | C/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157182 | CTTGATCCAGGACAG[C/T]TGCAGTGATTTCCAC | 25831 |
rs750560486 | snp | C/T | 4.97698e-05 | 0.00498823 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31113921 | TTCTGTTTTTCCTAA[C/T]ACTTTTATTAGTGCC | 25831 |
rs750564113 | snp | C/T | 0.000748596 | 0.0193323 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148774 | TGCCTCTTTTGCCAG[C/T]CCAGCCAGTCACAAA | 25831 |
rs750580961 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124983 | CGGTTAGTTTTTGTA[-/T]TTTTTAGTAGAGACA | 25831 |
rs750619285 | snp | A/T | 1.8806e-05 | 0.00306637 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144977 | AATGTGAATTTTTAC[A/T]ATTAATAATTTTACC | 25831 |
rs750621764 | snp | A/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164186 | CTGTCTGCCTTTTAT[A/T]TCCTGAACAGATACT | 25831 |
rs750626805 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165161 | GTCAGCTCATAATAC[C/T]GGTATTTGAGGTACT | 25831 |
rs750633915 | snp | C/T | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168388 | ATTTCCGGATCTCCT[C/T]TGGGCTCATTACATT | 25831 |
rs750642654 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127745 | ATAAAAGCATCATTA[C/T]GAAAGTATCTAAATA | 25831 |
rs750650907 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115010 | GACCCCTGTCATACA[C/T]GGTCCATCACTGACT | 25831 |
rs750664218 | in-del | -/CT | 1.65608e-05 | 0.00287752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122904 | AAAGAGAATGGGGTA[-/CT]CTCTCTACCATAACC | 25831 |
rs750672188 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182719 | TAGCCAGCATGGTGG[C/T]GTGCGCCTGTAGTCC | 25831 |
rs750684471 | snp | C/T | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31100082 | AGCTCTTAAGTCTGA[C/T]GACTGCATTGAAATA | 25831 |
rs750688459 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103264 | TAAAAAAGAATGGGC[C/T]GGGCACGGTGGCTCA | 25831 |
rs750699847 | snp | A/G | 1.65636e-05 | 0.00287776 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122979 | CATCTTCTTCATCTG[A/G]CTCAGGTAAGTCCTC | 25831 |
rs750708787 | snp | A/G | 4.96981e-05 | 0.00498463 | missense | HECTD1 | GRCh38.p7 | 14:31105415 | TGTTTCTGAATACCC[A/G]TATGCATACAAAAGT | 25831 |
rs750709796 | snp | A/G | 1.65633e-05 | 0.00287774 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168284 | CTAACACATCAAATA[A/G]TATGAATAACTACCT | 25831 |
rs750730048 | snp | C/T | 1.67823e-05 | 0.0028967 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103073 | TAAACCCATCTACAT[C/T]GTACATGTAACGGAA | 25831 |
rs750748232 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174460 | TGAGGCAGGACAATC[A/G]CTTGAACCCGGGAGG | 25831 |
rs750748737 | snp | C/T | 4.98252e-05 | 0.004991 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133286 | CCTGTGGGCTGCCAT[C/T]CTGATCTCGCCATTT | 25831 |
rs750752853 | snp | C/G | 1.67998e-05 | 0.00289821 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121550 | GTCTAATTATTTGAC[C/G]CATATATGCCCCCTT | 25831 |
rs750772670 | snp | C/G | 2.08375e-05 | 0.00322774 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173793 | GCAAAGCATCGCAGA[C/G]CTCCATCTGAAACCT | 25831 |
rs750810157 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189731 | GAGCTGCATTCCAGC[A/C]TGGATGAGAGTGAGA | 25831 |
rs750814103 | snp | A/G | 1.684e-05 | 0.00290167 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173691 | CCACCAGCAGCAGCC[A/G]TTCGAGATAACAGCT | 25831 |
rs750846144 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175620 | TGTAATCCCAACACG[C/T]TGGGAGGCCGAGGCG | 25831 |
rs750873856 | snp | G/T | 1.76693e-05 | 0.00297226 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129462 | GCCTGGAAAGGGACA[G/T]GAGTTTGTGAGACCC | 25831 |
rs750880876 | snp | C/T | 1.66738e-05 | 0.00288732 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173579 | CAGACTTACAATTGT[C/T]GACACCTGATTACTC | 25831 |
rs750898214 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200954 | GTTTTCCCTATTAGA[C/T]TATTAGGCACATAAG | 25831 |
rs750902252 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189054 | AACAGAACTGCAGAC[A/C]CAACTGCCTCCCCTA | 25831 |
rs750927237 | in-del | -/GGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127494 | GTAGCTGGGATTACA[-/GGC]GTGTGCCACCACTCC | 25831 |
rs750929656 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108206 | AGGCGATTTTCCTGC[C/T]TCGGCCTCCCAAGTA | 25831 |
rs750978534 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153203 | CGAGACCATCCTGGC[C/T]AACACGGTAAAACCC | 25831 |
rs751014789 | snp | C/T | 2.39123e-05 | 0.00345768 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141892 | CACTAAAGGCAGTTT[C/T]AAAAACATTTATTCT | 25831 |
rs751016159 | snp | A/G | 3.32674e-05 | 0.0040783 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109648 | CGTTAACAGCTGAAT[A/G]TACTACTAAACCAGC | 25831 |
rs751048735 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201118 | TTACCACTGTGTTCA[A/G]TAACTTTGGAATCCA | 25831 |
rs751065468 | snp | A/T | 3.32845e-05 | 0.00407936 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119684 | TATGTATTAAAATTA[A/T]ATCACAAAACCAAAA | 25831 |
rs751067802 | snp | A/T | 1.67764e-05 | 0.00289619 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116464 | TGAGGGGTCCCTAAA[A/T]ATTTGGAAGATGGGT | 25831 |
rs751118254 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144418 | CAGAGGTCAGCAAAC[A/G]TTTTCGTAAAGGGCC | 25831 |
rs751134191 | snp | G/T | 1.73171e-05 | 0.00294249 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140033 | TTAAGAGGTTTTGTA[G/T]AACTACATGTAAATG | 25831 |
rs751136215 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150169 | GACCAGTCTCTCCAA[C/T]GATATGGTTTACCTT | 25831 |
rs751148204 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201420 | AAATGCCCATAATAC[A/T]TATTTATAACATTAA | 25831 |
rs751223641 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134436 | TATGTTGAACATTCC[G/T]AAGTATTATGTGATT | 25831 |
rs751237922 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120357 | CCACTACACTCTGTA[C/T]TCCACCCCGGGAGAC | 25831 |
rs751260548 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200046 | ATCCAAACCCAAACT[C/G]ATGATCTCAATCTCT | 25831 |
rs751270438 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189055 | ACAGAACTGCAGACA[A/C]AACTGCCTCCCCTAC | 25831 |
rs751282904 | snp | A/G | 1.65671e-05 | 0.00287807 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128862 | AAGAGGTCGTTGTGA[A/G]GCTGCTTCTTTATTA | 25831 |
rs751328778 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31172010 | ATTAATATTTCTATC[C/T]TTAATTTAAATACCA | 25831 |
rs751336174 | snp | A/G | 1.65707e-05 | 0.00287838 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128658 | ATTAGTGTTGTTATC[A/G]CTGCTGCTTCGGCTT | 25831 |
rs751337934 | snp | C/T | 1.66615e-05 | 0.00288626 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135170 | CAAGTCCATAGGCAG[C/T]TGGATTTACCCATTC | 25831 |
rs751399298 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194176 | TGATTCCATTTACAT[A/G]ACATTCTAGAAAAGT | 25831 |
rs751403179 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145836 | CTTACAATTTCAACT[A/T]TTATTTTAGATTCGG | 25831 |
rs751408962 | snp | A/G | 4.97269e-05 | 0.00498608 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31106738 | CTCATCTTCAGAAAG[A/G]CCTTTGTTGCTTAAA | 25831 |
rs751416755 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31168208 | TTTTTAACATTAAAA[G/T]AAACCTCAAATACTT | 25831 |
rs751423256 | snp | A/G | 3.34102e-05 | 0.00408705 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144868 | ATGTTTCTGAGTGTT[A/G]CCACTACTCCACGAG | 25831 |
rs751429096 | snp | C/T | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178160 | CATCCAGGTAGTATG[C/T]TATGGCACGGGCTGT | 25831 |
rs751429293 | snp | A/T | 1.76614e-05 | 0.0029716 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144951 | TCGTACCTACCAAAA[A/T]AAACACAACAAATGT | 25831 |
rs751450747 | in-del | -/AT | 3.42959e-05 | 0.00414087 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157318 | CCTTGAAAAGTAAAA[-/AT]AGAATTATATGAAGC | 25831 |
rs751454876 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133051 | TCCAAAATACTACCA[A/G]TAAGTTTCTAGTCAA | 25831 |
rs751459067 | snp | C/T | 1.65806e-05 | 0.00287924 | missense | HECTD1 | GRCh38.p7 | 14:31113445 | GAGTAGAAATGGCCC[C/T]CTGGTTTAACCCAGA | 25831 |
rs751472299 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163447 | CCCCTTTCCTCCCCC[-/A]AAAGAATTAGCTGGG | 25831 |
rs751496720 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115592 | GGTAAAAACCCCATC[A/C]CTACAAAAAATACAA | 25831 |
rs751510416 | snp | C/T | 9.9552e-05 | 0.00705451 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121495 | CGTTGCAGGGATGGG[C/T]GTCTCAGAATCTAAA | 25831 |
rs751510524 | snp | C/G | 3.31246e-05 | 0.00406955 | missense | HECTD1 | GRCh38.p7 | 14:31113322 | TTGCAACTATATATA[C/G]AATACGCAGAAGCTG | 25831 |
rs751526747 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102170 | ATATGGTGATTAGAT[A/T]AATAGAAAAGAATAT | 25831 |
rs751564416 | snp | A/C | 1.65663e-05 | 0.002878 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173400 | TGCACTTTCAATTGA[A/C]TCTGGAAGCTCCGAC | 25831 |
rs751568766 | snp | A/G | 4.96824e-05 | 0.00498385 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129155 | CAATTTCTGATCTCC[A/G]TTCCGTTTTGGTCGA | 25831 |
rs751617378 | snp | C/T | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100302 | ATCTTTATTTTTGAG[C/T]TGCAAACACACTTAA | 25831 |
rs751636123 | snp | C/T | 1.65655e-05 | 0.00287793 | missense | HECTD1 | GRCh38.p7 | 14:31101049 | TGACTGATGGATAGC[C/T]TGCATCAGTAGCATC | 25831 |
rs751642807 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171159 | GCTCACACCTATAAT[C/G]CCAGCACTTTGGGAG | 25831 |
rs751663593 | snp | C/T | 1.65968e-05 | 0.00288065 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107585 | ACGAGATTCATCATC[C/T]GGAAAATTATCATCA | 25831 |
rs751684470 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187177 | ATGTGGCAAAACCTC[A/G]TCTCTACTAAAAAAC | 25831 |
rs751686458 | in-del | -/TCA | 1.65641e-05 | 0.00287781 | cds-indel, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122993 | GGCTCAGGTAAGTCC[-/TCA]TCATCATCGAGCTCA | 25831 |
rs751715966 | snp | A/C | 1.65619e-05 | 0.00287762 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136639 | AGGTGCACGTTCCAA[A/C]CGAAATCGTAATCTC | 25831 |
rs751719496 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196659 | CTCAGAAGGCTAAGG[C/T]AGAAGCATTGCTTGA | 25831 |
rs751721983 | snp | A/G | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173258 | TATCTAATCTCCGGA[A/G]TCCTGGGATTCTGCC | 25831 |
rs751730862 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152551 | ATCATCACATTTACA[A/G]TATCCAGTAGCAAAT | 25831 |
rs751742308 | snp | A/C | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205910 | CTGTAGCCATTCCAG[A/C]AATGTATCTGGGTCC | 25831 |
rs751772853 | snp | C/T | 1.6593e-05 | 0.00288031 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148872 | TTTATTTGTACCCAA[C/T]AAACTTACATATCTA | 25831 |
rs751788308 | snp | A/G | 0.00025104 | 0.0112008 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107269 | CTAATTTTTTAGAGG[A/G]TGAAATGCAAATAAA | 25831 |
rs751795699 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116975 | AAATAATTACACCTA[C/T]GTTACTGAAAGAGTG | 25831 |
rs751809782 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135998 | ACTCCAGCCTGGCAA[C/G]AGAGCAAGACTCTGT | 25831 |
rs751819907 | snp | C/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208423 | TGTGGCTTGTGGTCA[C/G]AAGTATGTCTGTGGT | 25831 |
rs751821258 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104065 | GTGGATGAAGAGAGG[G/T]AGTTTAATGGGTACA | 25831 |
rs751822348 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148800 | ACAAATTCTGAACCT[C/T]GGGGGGAAAAAAAAG | 25831 |
rs751841726 | snp | A/G | 3.55347e-05 | 0.00421498 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114100 | GCCTTTCCCAATTAT[A/G]AAGTCTATGATATTT | 25831 |
rs751868302 | snp | C/T | 0.000558503 | 0.0167015 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123652 | GGACTAAAGGGATTA[C/T]AACAGAAGTTTTTAC | 25831 |
rs751873608 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104923 | GCTCAAGCGATCCTC[C/T]TGCTTCAGCCTCCCA | 25831 |
rs751891440 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129509 | GAGCGTGTCAGACAG[C/T]AGCTCCACAATATGG | 25831 |
rs751921006 | snp | C/T | 8.35541e-05 | 0.00646297 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133438 | TAGAAATTGGAGAAA[C/T]AAAAACCAAATCACT | 25831 |
rs751922779 | snp | A/C | 1.65734e-05 | 0.00287862 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169358 | GTAGCTCTCACCTGG[A/C]GACTGAAGAATAGCT | 25831 |
rs751943865 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125028 | GCCAGGCTAGTCTCG[-/T]AACTCCTGACCTTGT | 25831 |
rs751947684 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190493 | ATACCATAGAAACAT[A/G]TAATGTACAAAGTGA | 25831 |
rs751948346 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195492 | AATTTTCCTTGTATT[C/T]TTCCTGTTGAAACTA | 25831 |
rs751963578 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177024 | ATCTAGCACTAATGC[G/T]TTTAGAGTTACATAA | 25831 |
rs751964804 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127222 | TCAAGTGGTCCGCCC[A/G]CCTTGGCCTCCCAAA | 25831 |
rs751975926 | snp | A/G | 1.65627e-05 | 0.00287769 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168417 | TTCTTCTTCATCTTT[A/G]TTTGTATCTTTCTTT | 25831 |
rs751999921 | snp | C/T | 1.6566e-05 | 0.00287797 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31123003 | AGTCCTCATCATCAT[C/T]GAGCTCAGCCAATAG | 25831 |
rs752018095 | in-del | -/GTTC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180341 | TGGGAGGCTGAGGCA[-/GTTC]AAGATCAGCTTGGCA | 25831 |
rs752035560 | snp | C/T | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127890 | CAACTGATAAAACTG[C/T]TGTTGCTGTAGCTAC | 25831 |
rs752038815 | snp | C/T | 6.86664e-05 | 0.00585905 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141937 | TACAATCTTGTTTCA[C/T]ATCCAAATCCATGCT | 25831 |
rs752043902 | snp | C/G | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099890 | ACACAAGTAACTGGT[C/G]AGTTCTAGCTGAGGC | 25831 |
rs752093770 | snp | C/T | 4.27981e-05 | 0.00462571 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141994 | CAAAAAAAAATAATT[C/T]AAGGATCTTACTGAA | 25831 |
rs752111543 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199714 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 25831 |
rs752137954 | snp | C/T | 8.28164e-05 | 0.00643439 | missense | HECTD1 | GRCh38.p7 | 14:31105467 | CTTCTGCATTATCCA[C/T]TGTTATCATCTGCAA | 25831 |
rs752142523 | snp | C/T | 4.97475e-05 | 0.00498711 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133319 | AATCCAGGCCTCTGA[C/T]AACACGAGCTCCTGG | 25831 |
rs752145741 | snp | C/T | 1.69568e-05 | 0.00291172 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173702 | AGCCATTCGAGATAA[C/T]AGCTCCTCAGTTAAT | 25831 |
rs752186933 | in-del | -/G | 9.94275e-05 | 0.0070501 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148801 | CAAATTCTGAACCTT[-/G]GGGGGAAAAAAAAGA | 25831 |
rs752192554 | snp | C/T | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099995 | TACCCGTATTTACTA[C/T]AGAAAAACACATTTC | 25831 |
rs752201814 | in-del | -/G | 4.98608e-05 | 0.00499279 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169335 | TAGATGGCTTCAAAA[-/G]AAAGAATGTAGCTCT | 25831 |
rs752205538 | snp | C/T | 1.85365e-05 | 0.00304433 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174868 | GGAACACTAAAAAAA[C/T]CACTTTCTGAAAATG | 25831 |
rs752220141 | snp | A/C | 1.65707e-05 | 0.00287838 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175044 | GTGTCTTTATGAACT[A/C]GATGTCCACTGTCAC | 25831 |
rs752240270 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157712 | GAGGCTGAGGGAGGC[A/G]GATCGCTTGAGGTCA | 25831 |
rs752243699 | snp | C/T | 9.97576e-05 | 0.00706179 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113090 | TGAAGAGTTCAGCTG[C/T]CTGATTTTATTACCT | 25831 |
rs752250253 | in-del | -/TAAC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160600 | ATTTTTTAAGTTTCT[-/TAAC]TGTCTAATAGGTAAA | 25831 |
rs752259377 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31128282 | ACAAAAGCTATACTT[A/G]TATGATGCTTTGGTT | 25831 |
rs752264414 | snp | A/G | 1.67666e-05 | 0.00289534 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150265 | ATGGAAAATAATTTC[A/G]ATTTCAAATATTCAT | 25831 |
rs752265823 | snp | A/C | 0.000282792 | 0.0118876 | intron-variant | HECTD1 | GRCh38.p7 | 14:31143996 | TAGAAATATTAACAT[A/C]ATTCAGCTTTTAAAT | 25831 |
rs752273677 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143659 | TTTATGATATGCTTA[C/G]GTAGGCTTATAACTT | 25831 |
rs752301541 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194902 | AAGATTGGCAAAGAC[A/G]TGAAAGAATATAACT | 25831 |
rs752316549 | snp | G/T | 4.5043e-05 | 0.00474547 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141922 | TTTCTACCAGTTGAC[G/T]ACAATCTTGTTTCAT | 25831 |
rs752356062 | snp | A/G | 1.66172e-05 | 0.00288242 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31112516 | CACACCAGTCTGGCA[A/G]AGCCCCACTTGCCAG | 25831 |
rs752374221 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31109765 | CTGCTTCCTGTCACA[A/G]GTAAAAATATATGAA | 25831 |
rs752409885 | snp | C/T | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173234 | GCCGATGTGAGCGCT[C/T]CCCAGAACTATCTAA | 25831 |
rs752414874 | snp | C/G/T | 6.62706e-05 | 0.005756 | missense | HECTD1 | GRCh38.p7 | 14:31100992 | CTCTCATGATCTCCT[C/G/T]GGAAGAATATTCAGG | 25831 |
rs752431012 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111770 | GAGTGCTTAATGTGC[C/T]CAATATGCACATTAA | 25831 |
rs752431149 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143931 | CAAAATAAACAATTA[C/T]TTAATTCATTTGGCT | 25831 |
rs752497387 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135785 | AGCACTTTGGGAGGC[A/G]GAGGTGGGTGGATCA | 25831 |
rs752517144 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114997 | TATAATCTTATGGGA[A/C]CCCTGTCATACATGG | 25831 |
rs752521135 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201449 | AATACATATGATGAT[C/T]ACCTATTTTGATGTG | 25831 |
rs752533007 | snp | C/T | 1.65627e-05 | 0.00287769 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129006 | AGCATTTTCACTTCC[C/T]GTTTCCGCTGTTAAG | 25831 |
rs752535940 | snp | A/T | 0.000202843 | 0.0100688 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116472 | CCCTAAAAATTTGGA[A/T]GATGGGTGAAAAACA | 25831 |
rs752563224 | snp | A/C | 0.000390927 | 0.0139754 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103092 | CATGTAACGGAAACA[A/C]AAAAAACAAACATAC | 25831 |
rs752582695 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148376 | AACCCAGATTGTAAA[A/G]TACAAGTCATTTTCA | 25831 |
rs752588141 | snp | C/T | 3.32873e-05 | 0.00407953 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135540 | GCTGGTGCCGAAATA[C/T]AAAATTTTGTCCTTC | 25831 |
rs752589825 | snp | A/C | 1.66269e-05 | 0.00288326 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31113902 | GCTATGAGCTGAGAA[A/C]AATTTCTGTTTTTCC | 25831 |
rs752594723 | snp | C/T | 1.66139e-05 | 0.00288213 | missense | HECTD1 | GRCh38.p7 | 14:31107019 | ACTCATAAATCAGTT[C/T]ACTCATATTGCTTTT | 25831 |
rs752599865 | in-del | -/AGTT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139411 | ACAATGTGAGAACAC[-/AGTT]AGAAGGTTCCATCTA | 25831 |
rs752602451 | snp | C/T | 3.9767e-05 | 0.00445891 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173133 | ACAACTTTCTTTTTA[C/T]ATTTAAAAAAATATT | 25831 |
rs752608062 | snp | A/G | 4.40733e-05 | 0.00469411 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135238 | AATAACAACGTTAAG[A/G]TAATTGCATTTGCAC | 25831 |
rs752647827 | snp | C/T | 1.66485e-05 | 0.00288513 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31106924 | CTCTTCAAAGCTTCC[C/T]ACCGAGAGTGAATCA | 25831 |
rs752671358 | snp | A/G | 1.65669e-05 | 0.00287805 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157190 | AGGACAGTTGCAGTG[A/G]TTTCCACTAGTATTG | 25831 |
rs752677798 | in-del | -/TCT | 1.65622e-05 | 0.00287764 | cds-indel | HECTD1 | GRCh38.p7 | 14:31113345 | AGAAGCTGAAGGACA[-/TCT]TCTACTCCACAAGAG | 25831 |
rs752695732 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31121596 | ATATATTAACCCCTA[G/T]TAACAAAAGTGTCAC | 25831 |
rs752711297 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112663 | TGCCCAGGCTGGTGT[A/G]CAGTGGTACGATCTC | 25831 |
rs752747147 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103603 | GGAACTGGAGGTCAT[C/T]ATATTAAGTGAAAAA | 25831 |
rs752755403 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161065 | CAAATGGCTCTGAAA[C/T]TTTTACGATCAATTT | 25831 |
rs752758151 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31172373 | CTCTGGGAGGCCGAG[A/G]TGGGAGGAGGTCAGG | 25831 |
rs752768278 | snp | C/T | 1.6585e-05 | 0.00287962 | missense, nc-transcript-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121415 | GGCTCCCTGCTCCAG[C/T]AGGTACCTGTGGTAG | 25831 |
rs752805675 | snp | C/T | 1.70292e-05 | 0.00291793 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101351 | AAAATATAGTTATAT[C/T]GAGTTGACTGCAGAT | 25831 |
rs752825325 | snp | C/G | 1.66255e-05 | 0.00288314 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156989 | TGATCTGCAAAGCCA[C/G]CAAGTGGCCATCATC | 25831 |
rs752829693 | snp | C/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208160 | ACCCGCACTCAGCCA[C/G]GATCTTCCCTCCTCG | 25831 |
rs752854639 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206064 | ACCAAATTTTCATAG[C/T]GTCCTCCTAGCAATT | 25831 |
rs752858529 | snp | C/T | 4.97393e-05 | 0.0049867 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173412 | TGAATCTGGAAGCTC[C/T]GACCTCAGAAGATCC | 25831 |
rs752882123 | in-del | -/AG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118028 | TTTTTTGTTCGAGAC[-/AG]AGTCTCACTCTGTCA | 25831 |
rs752890284 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139353 | CATGAATGGGATTAG[C/T]GTCCTTATAAAAGAG | 25831 |
rs752896331 | snp | C/T | 1.65605e-05 | 0.0028775 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129167 | TCCGTTCCGTTTTGG[C/T]CGAACCCAAGCTGAT | 25831 |
rs752942865 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154504 | GGTTTCACAATGTTG[G/T]CCAGGCTGGTTTCGA | 25831 |
rs752959215 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131436 | GCAGCAAAAATGAAT[C/T]GAGAAGAAAAATAAC | 25831 |
rs752959788 | in-del | -/TTCT | 1.65718e-05 | 0.00287848 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101114 | CATGAGTTTAAATAC[-/TTCT]TTCTTTCAAAAGTAA | 25831 |
rs752962993 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163377 | GAGCCTGGGAGGCAG[A/G]GCCTGCAGTGAGCCA | 25831 |
rs752971159 | snp | A/T | 1.65921e-05 | 0.00288024 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107669 | AAACTCTAATGTGGG[A/T]CCCAAGCCAGTTCCT | 25831 |
rs752975976 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196976 | CAATCTCTTCAATTC[A/T]CTCCTTCAGTATCTG | 25831 |
rs752990245 | snp | C/T | 1.69578e-05 | 0.0029118 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116192 | TGCTTCTTGGCTCTA[C/T]ACTAGGACATTATCT | 25831 |
rs753043488 | snp | A/C | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127910 | GCTGTAGCTACATTG[A/C]TGCTGCTAGTAACAC | 25831 |
rs753054988 | snp | C/T | 6.62712e-05 | 0.00575597 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149008 | CATCTGAATTATGAA[C/T]AGCAATTTCTCCTTC | 25831 |
rs753056307 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151076 | CCAGCCTGGGTAACA[C/G]ATCGGGACTCTGTCT | 25831 |
rs753087211 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186072 | CTTCCTTCCTAGATT[C/T]CCTCGTCATCTTTCC | 25831 |
rs753106641 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178573 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACCTGAG | 25831 |
rs753131747 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198478 | AAACTTGTATTTGAC[A/T]CCATGAGCTTGAAAG | 25831 |
rs753136925 | in-del | -/GTGTGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134564 | TGTGTGTGTGTGTGT[-/GTGTGC]GCGCGTATGTATATA | 25831 |
rs753143994 | snp | C/T | 4.92114e-05 | 0.00496017 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114250 | CTTCTTTTAACTAAA[C/T]AGCCAAGAGTAAACC | 25831 |
rs753179806 | snp | A/G | 3.31868e-05 | 0.00407336 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148881 | ACCCAATAAACTTAC[A/G]TATCTACATACTTAC | 25831 |
rs753183548 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129546 | CTTTTCATCAGTGCT[A/G]TCCTTTTCTGAATTT | 25831 |
rs753203771 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179070 | AAAGAACAGCAACTG[C/T]GTGACTTTTCTGCGT | 25831 |
rs753214481 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165575 | TCATAGGTTATAAAA[A/C]GCTCCTCTCTACTTT | 25831 |
rs753221658 | snp | C/G | | | missense | HECTD1 | GRCh38.p7 | 14:31107093 | GGTAAGTCCACAAGT[C/G]TATTGTCTTGAATGC | 25831 |
rs753228146 | snp | A/C | 1.66294e-05 | 0.00288347 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133613 | CCCATCTGTTTAATT[A/C]TCACATGTCTCCACC | 25831 |
rs753251308 | snp | C/T | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100775 | TTTTGTCATTAGCAG[C/T]TAAAAAACTTATTCC | 25831 |
rs753269796 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151681 | AGGCATGAGCCACCG[C/T]GCCTGACTCAGCATG | 25831 |
rs753294888 | snp | A/C | 1.65663e-05 | 0.002878 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169451 | CAGATCTGGATTTGC[A/C]CCATGCCGTAACAGA | 25831 |
rs753303643 | in-del | -/TTTTTTTTTT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199395 | GGTTTATTATTATAA[-/TTTTTTTTTT]TTTTTTTGAGACAGA | 25831 |
rs753341433 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178660 | TGCAAAAAATCAGCC[A/G]GGCGTGGTGACAGGC | 25831 |
rs753344070 | snp | C/T | 2.31742e-05 | 0.0034039 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133685 | GTTGACCTGTTAATA[C/T]GTTAGAGAAAAAATT | 25831 |
rs753344101 | snp | C/T | 1.73993e-05 | 0.00294947 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171869 | ACTTTACCTTTGCTA[C/T]TTGAGGTCTTCCAAA | 25831 |
rs753394228 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180482 | GTTTTTTGATAGTCT[C/T]GTTCTGTTGACCAGT | 25831 |
rs753398902 | snp | A/T | 3.66012e-05 | 0.00427776 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144218 | GGTTTTCTAAAGCTG[A/T]CTTCATTAAATCTCT | 25831 |
rs753410848 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117259 | CCGCCTGTAGTCCCA[C/G]CTACTCAGGAGGTTG | 25831 |
rs753421306 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112206 | TAGAAAACATCTATC[A/G]GGTATCTCTCCTCCT | 25831 |
rs753427362 | snp | G/T | 1.65798e-05 | 0.00287917 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175064 | TCCACTGTCACGAAT[G/T]AAGGTAAGCACACAA | 25831 |
rs753427397 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31150393 | GAAACATGGTCTCAA[C/T]TCTGTCATCCAGGCT | 25831 |
rs753438312 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166548 | GTGTGATATAATTAC[A/G]ATTTAAAGATATAAT | 25831 |
rs753448349 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131092 | GGTTGGTTTAAGTAT[C/T]TGAAAGCTAAGAACC | 25831 |
rs753504194 | snp | C/G | 1.65704e-05 | 0.00287836 | missense | HECTD1 | GRCh38.p7 | 14:31113300 | GATATTCTTGAATAA[C/G]GGTCACTTGCAACTA | 25831 |
rs753554391 | in-del | -/TGTG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134501 | TTTCCATTAGTGGGC[-/TGTG]TGTGTATGCATAAAT | 25831 |
rs753561621 | snp | C/T | 3.59266e-05 | 0.00423816 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31113155 | GCTAGTGAATTCATC[C/T]GGTGGAAAAGTAAAC | 25831 |
rs753577080 | in-del | -/CAT | 5.42667e-05 | 0.00520869 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127737 | AAAACATAATAAAAG[-/CAT]CATTATGAAAGTATC | 25831 |
rs753587862 | snp | A/G | 1.65693e-05 | 0.00287826 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101172 | CCCATTAGCCAGAGA[A/G]CTTGTACCTTGCGTA | 25831 |
rs753604009 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204295 | GTCAAACGGTATTTC[C/T]AGTTCTAGATCCTTG | 25831 |
rs753626442 | snp | C/T | 1.6566e-05 | 0.00287797 | missense, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119734 | GTATTTCTAGATCAG[C/T]TGTCTGCTGGACATT | 25831 |
rs753634884 | snp | C/G | 1.65811e-05 | 0.00287929 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156930 | ACCAAGTCTGGCTAG[C/G]TGATCCAAAAATATA | 25831 |
rs753657646 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191039 | TAACTCCCTGCTACC[C/T]GGATGTTTCAGGAGC | 25831 |
rs753665345 | snp | A/G | 1.65666e-05 | 0.00287802 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119852 | TCCTCCTTTAGTTTC[A/G]TACTCTTCTTCTTCC | 25831 |
rs753712447 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129140 | TACTGTGTTCCATTA[C/T]AATTTCTGATCTCCG | 25831 |
rs753725776 | snp | G/T | 1.70093e-05 | 0.00291622 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107236 | TCCAGGAGGTTTCAA[G/T]CCACCTCCAAGATCA | 25831 |
rs753727227 | snp | G/T | 1.65652e-05 | 0.0028779 | missense | HECTD1 | GRCh38.p7 | 14:31101002 | CTCCTCGGAAGAATA[G/T]TCAGGCAACTTAAGG | 25831 |
rs753748185 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129017 | TTCCCGTTTCCGCTG[C/T]TAAGGTGCTGGTGCT | 25831 |
rs753756662 | snp | A/C | 1.96084e-05 | 0.00313111 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156799 | TCCTCAAAAAAAAAA[A/C]AAAAACTCTTCCTGA | 25831 |
rs753762836 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170367 | AGCCCAGGAATTCAA[G/T]GTTACATGAGCTATC | 25831 |
rs753800607 | snp | A/G | 3.31246e-05 | 0.00406955 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136611 | CAGTCCTGTCAATCA[A/G]TGCAGTTTCACCAGG | 25831 |
rs753834433 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207510 | AGGTCGAACCGGGCA[G/T]GCGGCACAGGAAAAG | 25831 |
rs753879944 | in-del | -/TGTGTGTGTGTGTGTGCG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134553 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGCG]CGCGTATGTATATAC | 25831 |
rs753902081 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131279 | CTGTGGCAGCTAAAA[C/T]GAACAAACAAACAAA | 25831 |
rs753934645 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201990 | TGTCAAAATGGGTAC[A/C]AACAGTGGAGAGCCG | 25831 |
rs753958780 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164084 | AAGTACTCAGTCTAA[C/T]TATCTTACAGAGAAA | 25831 |
rs753986988 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155618 | TTCTCTTCATAAACA[-/C]CAAAGCTATGAAAAT | 25831 |
rs753987396 | snp | C/T | 1.65649e-05 | 0.00287788 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168252 | ATAAATAAAACCATA[C/T]AATTGGTGTAATTTG | 25831 |
rs753988732 | in-del | -/ACAGGG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118474 | TAACTACCTTGTCAA[-/ACAGGG]ACCTTTATTCTCTCA | 25831 |
rs754020833 | snp | C/T | 1.67849e-05 | 0.00289692 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144889 | ACTCCACGAGGCATG[C/T]TTTCAACAGCTTTAA | 25831 |
rs754038853 | snp | C/T | 3.31285e-05 | 0.00406978 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157206 | TTTCCACTAGTATTG[C/T]AGGCAAATTGTGACC | 25831 |
rs754039409 | snp | A/T | 1.67228e-05 | 0.00289156 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173668 | CTGATGATGGTCCTG[A/T]AACAGTACCACCAGC | 25831 |
rs754051529 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174263 | TTATAAATACTGTCT[A/T]ATGCCTGGCACAGTG | 25831 |
rs754071599 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162407 | GTACCACTTAATAAA[C/T]AGTACCCCCTCCCCT | 25831 |
rs754109024 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31113841 | AAAGCACGAAGCCAT[C/T]TGCAATCAAAATAGT | 25831 |
rs754111897 | in-del | -/TATAGT | 1.68992e-05 | 0.00290677 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101340 | CTAAAAGAACAAAAA[-/TATAGT]TATATTGAGTTGACT | 25831 |
rs754119885 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158281 | TTTTTTTGGAGACAG[A/G]GTCTCGCTCTGTTGT | 25831 |
rs754140005 | snp | A/G | 1.65605e-05 | 0.0028775 | missense | HECTD1 | GRCh38.p7 | 14:31109473 | GACTCGCCACGTGGA[A/G]CTTTTACTCTTTCAT | 25831 |
rs754142906 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108051 | ATGGTGAACAGACTT[C/T]TGTGTGTCTCTGTGT | 25831 |
rs754149441 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206280 | CAAGCTTCAGGTCCC[A/G]CTACTGCTATCACTA | 25831 |
rs754189564 | snp | C/T | 1.65614e-05 | 0.00287757 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129302 | TGCTCCATGATTGCG[C/T]TGTGCCTGAAACAGT | 25831 |
rs754195624 | snp | C/G | 1.65974e-05 | 0.0028807 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139983 | AACTTTCGAATTAAC[C/G]CAACTGCTGGTCGAC | 25831 |
rs754217003 | in-del | -/ATAGATAGA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188117 | TAGATAGATAGATAG[-/ATAGATAGA]TAGATAGATAGATAG | 25831 |
rs754219573 | snp | G/T | 2.62271e-05 | 0.00362117 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149195 | GTTTCAAAATCTTAT[G/T]TCTTTCAAGTATGAC | 25831 |
rs754240675 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114127 | ATTTCACATGCATTA[C/T]ATGAGGTAGCTTTAA | 25831 |
rs754242120 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198607 | ATCTGTGTAACTCAG[C/T]GGACTGATATTTTCC | 25831 |
rs754243031 | snp | A/G | 1.6566e-05 | 0.00287797 | missense | HECTD1 | GRCh38.p7 | 14:31116321 | ATTTTTGTACATAGT[A/G]AAAGATGGTTGATCT | 25831 |
rs754249275 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31172571 | ACTGCACTCCAGCCC[A/G]CACAACAGAGCGAGA | 25831 |
rs754260794 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167662 | TACACTGTAGAGGGA[A/G]AGCCACAAGGAGTTC | 25831 |
rs754270367 | snp | A/T | 1.67618e-05 | 0.00289493 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107720 | CTAAAATATGAACAA[A/T]TAAATTGTGGGTTAA | 25831 |
rs754280320 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147486 | CACAGGACTGGCACA[A/G]TGGCAAATGCCTGTA | 25831 |
rs754293053 | in-del | -/TTAAT | 1.6799e-05 | 0.00289814 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172011 | TTAATATTTCTATCC[-/TTAAT]TTAAATACCAGCTTT | 25831 |
rs754306033 | in-del | -/TGC | 1.68185e-05 | 0.00289982 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112572 | ATAATAATGTCTTAG[-/TGC]TGCTATAAGGCATTC | 25831 |
rs754310043 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118898 | ACTCCATCTCAAGGG[-/A]AAAAAAAAAAAAAAA | 25831 |
rs754314172 | snp | C/G | 1.66214e-05 | 0.00288278 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136717 | TTGGTTTCTGTCTCA[C/G]AATTGTAAAAAATGA | 25831 |
rs754320689 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118477 | CTACCTTGTCAAACA[G/T]GGACCTTTATTCTCT | 25831 |
rs754324679 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139437 | TCCATCTAAGAGGAA[C/T]AGGCCCTCACGAGAC | 25831 |
rs754341815 | snp | C/T | 1.65701e-05 | 0.00287833 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149033 | TCCTTCTTTCAAACA[C/T]GTCAGTGACCAATTT | 25831 |
rs754359851 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204555 | TAAAATACCAAAAGT[A/C]ACTTTCAGGTTACCT | 25831 |
rs754365702 | snp | A/G | 1.67775e-05 | 0.00289629 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116213 | GACATTATCTACCAA[A/G]ACATTAAGTTAAAAT | 25831 |
rs754446449 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194566 | TTTTTATTATCTTAA[A/C]GTGAGTACTATATTA | 25831 |
rs754466996 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126729 | GCCCTGTCACTGAGG[C/T]TGGAGTGCAGTGGCA | 25831 |
rs754486315 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101835 | CTGTCTTGAACTTAC[-/A]AAATTGTAAGAACTA | 25831 |
rs754508677 | snp | A/T | 2.3777e-05 | 0.00344789 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141893 | ACTAAAGGCAGTTTT[A/T]AAAACATTTATTCTT | 25831 |
rs754535562 | snp | A/T | 1.85293e-05 | 0.00304373 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133189 | ATTATCTTAAAAGAA[A/T]AAATTTAACTACCCA | 25831 |
rs754540929 | in-del | -/ATT | 1.6989e-05 | 0.00291449 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140011 | GACTGCGAAGAAATA[-/ATT]ATTATTAAGAGGTTT | 25831 |
rs754582653 | snp | C/T | 1.69496e-05 | 0.0029111 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112384 | ACATAAAAGCATACT[C/T]ATTCTAAAAACATAA | 25831 |
rs754612428 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31119995 | AAATGAGCTAACCTA[A/T]ACATGTATAGATACA | 25831 |
rs754613131 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108486 | TGCATAAAGTATAAT[A/C]AAAACTACAGCATAT | 25831 |
rs754633025 | snp | A/G | 1.65811e-05 | 0.00287929 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121435 | ACCTGTGGTAGCTGC[A/G]AGGTAACAGCATGAT | 25831 |
rs754635584 | snp | A/C | 1.67888e-05 | 0.00289726 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116465 | GAGGGGTCCCTAAAA[A/C]TTTGGAAGATGGGTG | 25831 |
rs754638523 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201315 | ATTTTTTAAATAAAG[A/C]CTACTAGCACCTAAA | 25831 |
rs754677311 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31168225 | AACCTCAAATACTTC[A/T]GGAAAAGGGAGATAA | 25831 |
rs754681289 | snp | A/G | 1.73589e-05 | 0.00294604 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149968 | AAACTGTAGAAACTA[A/G]GAAAATATTTTAATT | 25831 |
rs754687597 | snp | C/T | 0.000629316 | 0.0177274 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116370 | TTCAACTTCACGAGT[C/T]GTTCCAAGACCTGTT | 25831 |
rs754697962 | snp | C/T | 1.67944e-05 | 0.00289775 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172011 | TTAATATTTCTATCC[C/T]TAATTTAAATACCAG | 25831 |
rs754700432 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31121790 | ATCAATTTTTTTGAA[A/C]TCTAGTAACATTTTA | 25831 |
rs754705395 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189293 | AACTCGGTTTAGTAT[C/T]TGTCCTTAGAATTCC | 25831 |
rs754737197 | in-del | -/AAG | 3.50828e-05 | 0.0041881 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148693 | ATCAGTATAAAAGAC[-/AAG]AATAAAGCACATCCA | 25831 |
rs754746945 | snp | C/T | 8.47889e-05 | 0.00651055 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135231 | ATTAGCAAATAACAA[C/T]GTTAAGATAATTGCA | 25831 |
rs754769130 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155181 | GAAACCCTGTCTCTA[C/T]TAAAAATTCAAAAAT | 25831 |
rs754780800 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108229 | CCCAAGTAGGTGGGA[-/T]TACGGCATGCACCAC | 25831 |
rs754782224 | snp | G/T | 1.65663e-05 | 0.002878 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128869 | CGTTGTGAAGCTGCT[G/T]CTTTATTAGTTAATT | 25831 |
rs754811049 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133067 | TAAGTTTCTAGTCAA[A/T]ACCCAAGAACTTAAA | 25831 |
rs754822380 | snp | C/T | 1.66679e-05 | 0.00288681 | missense | HECTD1 | GRCh38.p7 | 14:31106896 | GATCAAGAATAAATT[C/T]TGATTTTGAATCCTC | 25831 |
rs754835705 | snp | G/T | 1.65669e-05 | 0.00287805 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128669 | TATCACTGCTGCTTC[G/T]GCTTAGATTCATGTT | 25831 |
rs754849406 | snp | C/T | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178168 | TAGTATGTTATGGCA[C/T]GGGCTGTCACCTCTA | 25831 |
rs754857131 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102235 | TCTGGATACCAATTA[C/T]ACAGGTGTGTTCATT | 25831 |
rs754875235 | snp | A/G | 1.6577e-05 | 0.00287893 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31106744 | TTCAGAAAGACCTTT[A/G]TTGCTTAAAATTTGG | 25831 |
rs754879975 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192062 | GCCAGGTGTGGTGGC[-/T]CACGTGTGTAATCCC | 25831 |
rs754895012 | snp | C/T | 1.66824e-05 | 0.00288806 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171931 | TGACCTCTATTAACA[C/T]CTGCACCTCTCTCAC | 25831 |
rs754902791 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131785 | AACAATTACAGGAAA[C/T]AGAATAACAACTTTT | 25831 |
rs754916449 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181219 | AGTATAAACTTAATA[C/T]ATTTCATGGGGGAAT | 25831 |
rs754941693 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138953 | CATTAGTAAAATGTA[C/T]TGTTTGTTTGCATCT | 25831 |
rs754965364 | snp | A/G | 1.65608e-05 | 0.00287752 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135000 | AGCATGACGAAGTGT[A/G]TATGCTGATGGTATC | 25831 |
rs754979001 | snp | C/T | 0.000289286 | 0.0120233 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156806 | AAAAAAAAAAAAAAC[C/T]CTTCCTGATACCTCT | 25831 |
rs754992476 | snp | A/G | 1.67153e-05 | 0.00289091 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144871 | TTTCTGAGTGTTACC[A/G]CTACTCCACGAGGCA | 25831 |
rs755006946 | snp | A/G | 1.65908e-05 | 0.00288012 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119895 | ATTTCACACACAAAC[A/G]TAATAAGATGCAAAA | 25831 |
rs755014760 | snp | C/T | 1.65696e-05 | 0.00287828 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101173 | CCATTAGCCAGAGAG[C/T]TTGTACCTTGCGTAC | 25831 |
rs755041236 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171168 | TATAATCCCAGCACT[C/T]TGGGAGGACAAAGCA | 25831 |
rs755047358 | snp | C/T | 1.65701e-05 | 0.00287833 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173403 | ACTTTCAATTGAATC[C/T]GGAAGCTCCGACCTC | 25831 |
rs755058172 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202119 | GTGAAACCTCGTTTC[C/T]ACTAAAAATACAAAA | 25831 |
rs755070818 | snp | A/G | 1.65666e-05 | 0.00287802 | missense | HECTD1 | GRCh38.p7 | 14:31101051 | ACTGATGGATAGCTT[A/G]CATCAGTAGCATCAA | 25831 |
rs755078023 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137735 | ACAGAGCTAGACCCA[C/G]TCTTGAAAAGAAAAA | 25831 |
rs755097057 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124265 | CCGGTATGTTACAAC[C/T]GACTGATGTCCCTTT | 25831 |
rs755097622 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136379 | TACAAAATTATAATA[A/C]ACATCTTCATGTAGA | 25831 |
rs755152978 | snp | C/T | 1.65619e-05 | 0.00287762 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136640 | GGTGCACGTTCCAAC[C/T]GAAATCGTAATCTCC | 25831 |
rs755176872 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185068 | ATGCTTCTGGCCGGG[C/T]GCGGTGGCTCACGCC | 25831 |
rs755176924 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196678 | AGCATTGCTTGAACC[C/T]GGGAGGCAGAGGTTA | 25831 |
rs755184865 | snp | C/T | 1.65611e-05 | 0.00287755 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129033 | TAAGGTGCTGGTGCT[C/T]GCACTGGAAGATGAC | 25831 |
rs755185625 | snp | A/G | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127994 | AAACTCTGAGCACCC[A/G]TAAGAGGAGAAGCTA | 25831 |
rs755202055 | snp | C/G/T | 4.97957e-05 | 0.00498957 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148880 | TACCCAATAAACTTA[C/G/T]ATATCTACATACTTA | 25831 |
rs755229884 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185998 | TTCTTTCACGGTCTG[A/G]AATGAGTATTTTCTT | 25831 |
rs755264307 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143876 | GAAGTGTTTTTAGTC[-/A]ACAAAACCTTTAGCA | 25831 |
rs755264541 | snp | C/T | 1.65718e-05 | 0.00287848 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205927 | ATGTATCTGGGTCCA[C/T]ATCTGCCATGGTTTT | 25831 |
rs755264822 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195579 | AGGCTGCAGCACAGT[A/G]GTGCAATTTCGGCTC | 25831 |
rs755274302 | snp | C/T | 0.000149141 | 0.00863414 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135658 | TCACCTTAATAATGC[C/T]GTTTTCAAGCACGTT | 25831 |
rs755280810 | snp | A/G | 1.66399e-05 | 0.00288438 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205774 | CAGTAACCCAAAGGA[A/G]CATGATGAAGGAATG | 25831 |
rs755326439 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151648 | CTGCCCTCCTCCATC[G/T]CAAAGTGCTGGGATT | 25831 |
rs755345710 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149302 | TATTAGCCAGGCATG[A/G]TGGTACGCATCTGTA | 25831 |
rs755368527 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116179 | AAAATAAATGCAATG[C/T]TTCTTGGCTCTACAC | 25831 |
rs755376785 | snp | A/T | 3.51587e-05 | 0.00419262 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127758 | TATGAAAGTATCTAA[A/T]TACTTTCATTTTAAA | 25831 |
rs755383813 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115184 | ATTTTTAAACTGTAA[C/T]AAAAATTGAAGGGAG | 25831 |
rs755399165 | snp | A/G | 1.65737e-05 | 0.00287864 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148801 | CAAATTCTGAACCTT[A/G]GGGGGAAAAAAAAGA | 25831 |
rs755444106 | snp | C/T | 3.31329e-05 | 0.00407005 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127947 | TTGACATAGTCACTG[C/T]TGATGTAGTACCAGG | 25831 |
rs755447456 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104116 | GAGTAAGTTCTAATG[C/T]TTTCTAGCATAGTAG | 25831 |
rs755466574 | snp | C/T | | | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173295 | TCCAGCACTAGACTT[C/T]GGCAAAGCTTTTCGT | 25831 |
rs755469395 | snp | A/G | 1.65638e-05 | 0.00287778 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31105447 | AAACATCAAATCCAC[A/G]TATTCTTCTGCATTA | 25831 |
rs755484347 | snp | C/T | 1.65649e-05 | 0.00287788 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168436 | GTATCTTTCTTTTTC[C/T]TATCATCTCCTTTAT | 25831 |
rs755525193 | snp | C/T | 0.000105457 | 0.00726069 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106229 | TGATAATTACCTGTA[C/T]ATAAAGTAACAGAGT | 25831 |
rs755531040 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209204 | CTGGACCTTGAAGAA[C/T]GGGTACAATGTAGAC | 25831 |
rs755537481 | snp | C/T | 1.65718e-05 | 0.00287848 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175047 | TCTTTATGAACTAGA[C/T]GTCCACTGTCACGAA | 25831 |
rs755546855 | snp | A/C | 5.65579e-05 | 0.00531749 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173842 | CCCACAGATAAAATC[A/C]ACCTAAAAAGGGTTA | 25831 |
rs755582430 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165584 | ATAAAAAGCTCCTCT[C/T]TACTTTCTTAACATT | 25831 |
rs755582885 | snp | C/T | 1.69332e-05 | 0.0029097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31127775 | ACTTTCATTTTAAAT[C/T]ACAACTTACCATATA | 25831 |
rs755592652 | in-del | -/A | 1.66172e-05 | 0.00288242 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169336 | AGATGGCTTCAAAAG[-/A]AAGAATGTAGCTCTC | 25831 |
rs755593426 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31128290 | TATACTTATATGATG[C/T]TTTGGTTTCACTGCA | 25831 |
rs755606352 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164429 | GCTGGGACCAGAAAC[A/G]TGCCACCGTGTGCTC | 25831 |
rs755612756 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177036 | TGCTTTTAGAGTTAC[A/G]TAAAGACAACAGCTT | 25831 |
rs755626157 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189581 | GCCTGGGCAACATAG[-/C]GAGATCCCATCTCTA | 25831 |
rs755632272 | snp | A/C | 3.31768e-05 | 0.00407275 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123052 | ATCAAGGAAATCTTG[A/C]AAACAAAACCCACAA | 25831 |
rs755648293 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129610 | ATGTAAATTTTTGGA[C/G]TCAATTATTTGACGA | 25831 |
rs755655947 | snp | C/T | 1.65853e-05 | 0.00287964 | stop-gained, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168465 | ATTAACTGGACACAT[C/T]CAATCACCTACAGAC | 25831 |
rs755718616 | snp | C/T | 3.31285e-05 | 0.00406978 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105491 | TCTGCAAAAGAAAAT[C/T]TGTCAGTATCTAGGA | 25831 |
rs755754787 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202881 | GGATCAGGAGATCAA[C/G]AGATGGAGACCATCC | 25831 |
rs755760722 | snp | C/T | 4.97484e-05 | 0.00498715 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133340 | GAGCTCCTGGAACCA[C/T]GTATTTCAGAACCTG | 25831 |
rs755769448 | snp | A/C | 1.85996e-05 | 0.0030495 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174869 | GAACACTAAAAAAAT[A/C]ACTTTCTGAAAATGG | 25831 |
rs755776072 | snp | A/C | 4.50552e-05 | 0.00474611 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141925 | CTACCAGTTGACTAC[A/C]ATCTTGTTTCATATC | 25831 |
rs755790055 | snp | A/C | 1.71378e-05 | 0.00292722 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144022 | TAAATATTTCTTGAC[A/C]AAACAAACTAAAAAC | 25831 |
rs755804046 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190769 | TCAAGCAATCCTCCC[A/C]CCTTGGCCTCCCAAG | 25831 |
rs755807387 | snp | C/T | 1.66244e-05 | 0.00288304 | missense | HECTD1 | GRCh38.p7 | 14:31112524 | TCTGGCAGAGCCCCA[C/T]TTGCCAGTGCCAATG | 25831 |
rs755840542 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201469 | ATTTTGATGTGAATA[C/G]AAAATGCTCATTAGC | 25831 |
rs755841325 | snp | A/C | 3.5775e-05 | 0.00422921 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156791 | CTAGATTTTCCTCAA[A/C]AAAAAAAAAAAAACT | 25831 |
rs755841545 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156738 | ACAGAATTATTTCAT[A/C]TTGTCATTATCCTGT | 25831 |
rs755856392 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142381 | TAAATGAGAATAAAT[A/G]CAAATAGTAAAGTTT | 25831 |
rs755862954 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147221 | GGAAGGCTGAGGCAG[C/G]AGAATCACTTGAACC | 25831 |
rs755874241 | snp | C/T | 4.96857e-05 | 0.00498401 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129012 | TTCACTTCCCGTTTC[C/T]GCTGTTAAGGTGCTG | 25831 |
rs755932717 | snp | G/T | 1.65715e-05 | 0.00287845 | missense, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119719 | CTGTACCTGGGGGTG[G/T]TATTTCTAGATCAGT | 25831 |
rs755950862 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170240 | ACATGGTGAGAGCTC[A/G]TCTCTACAAATAATA | 25831 |
rs755966462 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157752 | GACTAGCTTGGCCAA[C/T]ATGGAGAAACCCCGT | 25831 |
rs755977348 | snp | A/G | 1.71146e-05 | 0.00292524 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116485 | GAAGATGGGTGAAAA[A/G]CAATTATACTAAAAC | 25831 |
rs756009239 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120610 | ACTGAATTACTTATA[C/T]ACCAAATAAAATGCT | 25831 |
rs756014713 | in-del | -/A | 0.000186098 | 0.00964441 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123627 | TCTTCATAAAAACTG[-/A]AAAAAAAGAGGACTA | 25831 |
rs756018881 | snp | C/T | 3.32287e-05 | 0.00407593 | missense | HECTD1 | GRCh38.p7 | 14:31107021 | TCATAAATCAGTTTA[C/T]TCATATTGCTTTTAA | 25831 |
rs756058957 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102837 | GATACTCACTGAATT[-/A]AAAGTTCTTTAGAGA | 25831 |
rs756100603 | in-del | -/G | 1.67365e-05 | 0.00289275 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113500 | CTATAGAAACAATTA[-/G]AAAAACTGGCCATTA | 25831 |
rs756105364 | snp | C/T | 3.66482e-05 | 0.00428051 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173135 | AACTTTCTTTTTATA[C/T]TTAAAAAAATATTTT | 25831 |
rs756119928 | snp | C/T | 9.20598e-05 | 0.00678391 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135242 | ACAACGTTAAGATAA[C/T]TGCATTTGCACAAGG | 25831 |
rs756127197 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143977 | ACCTAAAGGCTGAAG[-/A]AATTAGAAATATTAA | 25831 |
rs756137642 | snp | C/T | 1.65622e-05 | 0.00287764 | missense | HECTD1 | GRCh38.p7 | 14:31113327 | ACTATATATAGAATA[C/T]GCAGAAGCTGAAGGA | 25831 |
rs756151318 | snp | C/T | 0.000165793 | 0.00910326 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121431 | AGGTACCTGTGGTAG[C/T]TGCGAGGTAACAGCA | 25831 |
rs756181826 | snp | A/C/T | 6.31617e-05 | 0.00561939 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144274 | TAAAAGAAAAAAAAA[A/C/T]TTAATGAAGGCAATC | 25831 |
rs756188875 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184610 | AGCTGGCATAGTGGC[A/G]CATGCCTGCAGTCGC | 25831 |
rs756189037 | snp | G/T | 3.32237e-05 | 0.00407563 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31172058 | TACCATTTCCTGAGT[G/T]CCAAAAGCAGAGGCC | 25831 |
rs756193266 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192566 | TAACCAGTATCAGGA[A/T]GAAAAAGGGGTTTAT | 25831 |
rs756195775 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161208 | TGGCTGCAGGTAATA[C/T]TGTTTCTGTTATGTA | 25831 |
rs756199108 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206086 | CTAGCAATTAAAAAA[A/G]ACTCCTAAGTACGTT | 25831 |
rs756217260 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162317 | GTTTTTAAGTCTTAG[A/G]ATTTGTTTAGATTTA | 25831 |
rs756218961 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124358 | CATCATAGAATAAAA[C/T]GTCTCTTCAAAACAC | 25831 |
rs756233177 | snp | C/G | 1.67357e-05 | 0.00289268 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157001 | CCAGCAAGTGGCCAT[C/G]ATCATCATCCTGAAA | 25831 |
rs756249045 | snp | A/T | 1.65666e-05 | 0.00287802 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157193 | ACAGTTGCAGTGATT[A/T]CCACTAGTATTGTAG | 25831 |
rs756278141 | snp | C/T | 1.65614e-05 | 0.00287757 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129300 | GCTGCTCCATGATTG[C/T]GTTGTGCCTGAAACA | 25831 |
rs756313193 | snp | A/G | 1.66109e-05 | 0.00288187 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119915 | AAGATGCAAAATTTC[A/G]TTGTTGCAAAAGCAA | 25831 |
rs756315204 | snp | A/G | 1.66877e-05 | 0.00288852 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173540 | ATGTGTTACTACCGG[A/G]GAGCCTCTGCAAAGT | 25831 |
rs756333643 | snp | A/G | 3.31603e-05 | 0.00407174 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173413 | GAATCTGGAAGCTCC[A/G]ACCTCAGAAGATCCT | 25831 |
rs756376986 | snp | A/C/G | 3.31347e-05 | 0.00407019 | missense | HECTD1 | GRCh38.p7 | 14:31101214 | CTGGGATGCAGGTTA[A/C/G]CCAGTCCACCTGGGG | 25831 |
rs756398533 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198522 | AAAAACTTGTCTGAT[A/G]AGAGTGGTAGTCATA | 25831 |
rs756402209 | snp | C/T | 4.96792e-05 | 0.00498368 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129168 | CCGTTCCGTTTTGGT[C/T]GAACCCAAGCTGATG | 25831 |
rs756433613 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186139 | TTCTCTTAGTTCATA[C/T]ACCACAAATATAAAT | 25831 |
rs756444790 | snp | C/T | 1.65908e-05 | 0.00288012 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136706 | TGGAAAACGTCTTGG[C/T]TTCTGTCTCAGAATT | 25831 |
rs756448775 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185858 | CCCCACATTCCCTAG[C/G]TCTGAATCTATGTCA | 25831 |
rs756455123 | snp | A/G | 1.6607e-05 | 0.00288153 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107678 | TGTGGGTCCCAAGCC[A/G]GTTCCTTCTTCTCCT | 25831 |
rs756458716 | in-del | -/GT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122154 | TGTGTGTGTGCTTGG[-/GT]GTGTGTGTGTGTCAG | 25831 |
rs756480550 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31106473 | CTAGTATTCTGAGTG[C/T]TGTCTTTATAATATT | 25831 |
rs756481054 | snp | A/C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171319 | TGGGAGGCTGAGGCA[A/C/T]GAGATCGTTTGAACA | 25831 |
rs756487173 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187453 | CCTCTTATACATCTA[C/T]ATAAGAGCTATGTCC | 25831 |
rs756492260 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105151 | GGATTACAGGTATGC[A/G]CCACCATGCCCAGCT | 25831 |
rs756500868 | snp | A/G | 2.48111e-05 | 0.00352207 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107299 | AATTAAACAAAAGTT[A/G]ATAGAAACTAAGCCT | 25831 |
rs756512002 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136745 | TGATATACCCTAAAA[C/T]AACTGAGATTTGGAT | 25831 |
rs756514296 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152780 | ACTTTGAGGTCACGA[A/G]TTCGAGACCACCCTG | 25831 |
rs756552264 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117216 | CGTCTCTACCAAAAA[C/T]GCAAAAATTAGCTGG | 25831 |
rs756556113 | snp | A/G | 2.40255e-05 | 0.00346586 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114267 | GCCAAGAGTAAACCA[A/G]TGTTCTAAAATAACT | 25831 |
rs756567081 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138215 | GTTCCAAGCATTTTG[A/G]ATAAGGAATACTCAA | 25831 |
rs756567278 | in-del | -/T | 1.6571e-05 | 0.0028784 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101148 | AGTAACTAAATTTCA[-/T]TTGGATTCCCCATTA | 25831 |
rs756567712 | snp | C/G | 1.69332e-05 | 0.0029097 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116197 | CTTGGCTCTACACTA[C/G]GACATTATCTACCAA | 25831 |
rs756573551 | snp | C/G | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136646 | CGTTCCAACCGAAAT[C/G]GTAATCTCCTTGTAA | 25831 |
rs756585011 | snp | C/T | 3.34633e-05 | 0.0040903 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31205973 | CTTAAATTTGAAAAG[C/T]AAAGGGAGAAAAGTC | 25831 |
rs756591245 | snp | C/T | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127923 | TGCTGCTGCTAGTAA[C/T]ACTGGATGTTGACAT | 25831 |
rs756624287 | snp | A/T | 1.65938e-05 | 0.00288039 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148884 | CAATAAACTTACATA[A/T]CTACATACTTACCCA | 25831 |
rs756629605 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200597 | CCAGCCTGGCCAACA[C/T]AGTGAAACCCGATCT | 25831 |
rs756639602 | snp | C/T | 3.31225e-05 | 0.00406941 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169417 | CTTTATCTAATGGAG[C/T]TTTCCCATCTTCATC | 25831 |
rs756673898 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166576 | AATTCTCAAGCCAAG[C/T]GCGGTAGCTCATGCC | 25831 |
rs756711001 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144498 | ATTCAACCACGCCCC[-/T]GTAGCACCAAAGTAG | 25831 |
rs756717127 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131131 | CATAGAGACTCAAAG[A/G]CATAACTTGATGGGA | 25831 |
rs756718008 | snp | C/T | 0.000150818 | 0.00868253 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116215 | CATTATCTACCAAAA[C/T]ATTAAGTTAAAATTT | 25831 |
rs756735019 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170461 | TCAATATATCCACCT[C/T]TATACCCACTAACAC | 25831 |
rs756745938 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117449 | ATTCTGGGCCAATGA[C/T]GTGTCAACCTTTTAT | 25831 |
rs756761424 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197212 | AATCAATTTTTAAGA[C/G]TATAACTCAGGGCCA | 25831 |
rs756772426 | snp | C/T | 1.65669e-05 | 0.00287805 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127953 | TAGTCACTGTTGATG[C/T]AGTACCAGGTGTGGT | 25831 |
rs756797663 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167763 | CCTAGAAAACTCCTA[A/G]GTATCCTTTAAACCA | 25831 |
rs756801071 | snp | A/C | 3.31274e-05 | 0.00406972 | missense | HECTD1 | GRCh38.p7 | 14:31105462 | ATATTCTTCTGCATT[A/C]TCCATTGTTATCATC | 25831 |
rs756826206 | snp | C/T | 1.65968e-05 | 0.00288065 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148888 | AAACTTACATATCTA[C/T]ATACTTACCCAGGGA | 25831 |
rs756879472 | snp | C/T | 1.65693e-05 | 0.00287826 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169458 | GGATTTGCACCATGC[C/T]GTAACAGAGTCTAGA | 25831 |
rs756895752 | snp | A/G | | | missense | HECTD1 | GRCh38.p7 | 14:31101193 | ACCTTGCGTACAACC[A/G]TGAGCCTGGGATGCA | 25831 |
rs756897529 | snp | A/G | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127832 | TCACTCTCACTGGAA[A/G]TTGATGTGAGGCTGG | 25831 |
rs756905439 | snp | A/G | 1.65825e-05 | 0.00287941 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175067 | ACTGTCACGAATGAA[A/G]GTAAGCACACAATTC | 25831 |
rs756907073 | snp | A/G | 6.69087e-05 | 0.00578358 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133476 | AAAGTAATTGTTTTA[A/G]TAAGTTAGAAAAGCC | 25831 |
rs756910689 | in-del | -/GGTGT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170135 | CCAAAAAGTCAACCA[-/GGTGT]GGTAGCTCACGCCTA | 25831 |
rs756928751 | snp | A/G | 2.80234e-05 | 0.00374311 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133694 | TTAATATGTTAGAGA[A/G]AAAATTATGTAATAT | 25831 |
rs756939339 | snp | A/G | 0.000138744 | 0.00832784 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106277 | AGCATCTCAACTGCT[A/G]CAGCCTTTGGTGATA | 25831 |
rs756958009 | snp | A/G | 1.79767e-05 | 0.00299801 | missense | HECTD1 | GRCh38.p7 | 14:31113159 | GTGAATTCATCTGGT[A/G]GAAAAGTAAACTGAA | 25831 |
rs756979673 | snp | C/G | 1.8927e-05 | 0.00307622 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144243 | ATCTCTCCAAGTGTT[C/G]TCACTCTCAATACAC | 25831 |
rs756984662 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142855 | TGGGAGGCCAAGGAA[A/G]GCAGATCGCTTGAGC | 25831 |
rs756984884 | in-del | -/ATA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188113 | TAGATAGATAGATAG[-/ATA]GATAGATAGATAGAT | 25831 |
rs756995227 | snp | A/G | 1.74415e-05 | 0.00295304 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174892 | GAAAATGGAAAGTAT[A/G]TAACAGCAACTTATT | 25831 |
rs756996989 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111306 | CGCCCAGGCTGGAGT[A/G]CAGTGGCACAATCTC | 25831 |
rs757006426 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204318 | GATCCTTGAGGAATC[A/G]CCACACTGTTTTCCA | 25831 |
rs757007707 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191092 | ATCCTCCTGCCTCAG[C/T]CTCCCAAAGCACTGG | 25831 |
rs757031701 | snp | A/C/G | 0.000101793 | 0.00713358 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144051 | ACCACTCTACCGAAG[A/C/G]AGTAACTACAAATAA | 25831 |
rs757049914 | snp | A/G | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100151 | TGATTATTGTTGAGC[A/G]TACATTTTGGAAATT | 25831 |
rs757069695 | snp | A/G | 4.97146e-05 | 0.00498546 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105539 | AGTACAACTGGCCTT[A/G]CTAAGAGGATATGTC | 25831 |
rs757084451 | in-del | -/TGT | 3.31263e-05 | 0.00406965 | cds-indel, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127888 | ACCAACTGATAAAAC[-/TGT]TGTTGCTGTAGCTAC | 25831 |
rs757106907 | snp | C/T | 1.78688e-05 | 0.00298899 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144173 | TTTCATATGGTGAAA[C/T]TGTGTTTTCATCCTT | 25831 |
rs757109633 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204903 | GTAATATAAACTTTA[-/T]TCCCACCTAAAACAC | 25831 |
rs757120053 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122719 | TTCTAAAATTTTTCA[A/G]ATATAAGCAACTTAT | 25831 |
rs757125150 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112246 | ATTAGTCATTTTGGC[A/G]AATTACTAGAAGATT | 25831 |
rs757160149 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110050 | TCTGTCACCCAGGCT[A/G]GAGTACAGTGGCATT | 25831 |
rs757182750 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158514 | ATCCGCCTGCCTCTG[C/T]CTCCCAGAGTGCTGG | 25831 |
rs757193282 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203084 | ACAGAGCAAGACTTC[A/G]TATGAAAAAACAGAA | 25831 |
rs757200120 | snp | A/C | 3.89719e-05 | 0.00441412 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156800 | CCTCAAAAAAAAAAA[A/C]AAAACTCTTCCTGAT | 25831 |
rs757205451 | in-del | -/G | 9.4526e-05 | 0.00687416 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135435 | ATTCTTTTACCAAGT[-/G]AATATGGTCACTCCA | 25831 |
rs757207097 | snp | C/T | 1.65644e-05 | 0.00287783 | missense, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119754 | TGCTGGACATTAGTA[C/T]GACCAGGTCTAGGAT | 25831 |
rs757217282 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201954 | AGAAGAAGTTATATT[C/T]GTTGAACTTCAGAAA | 25831 |
rs757248036 | snp | C/T | 1.65663e-05 | 0.002878 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101011 | AGAATATTCAGGCAA[C/T]TTAAGGTAATGCACA | 25831 |
rs757269778 | snp | A/G | 3.31241e-05 | 0.00406952 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173255 | AACTATCTAATCTCC[A/G]GAGTCCTGGGATTCT | 25831 |
rs757279140 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102367 | TTTACCAAATTTTAA[A/C]AATGAACAATTAAAA | 25831 |
rs757291163 | snp | C/T | 5.02004e-05 | 0.00500976 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113498 | TCCTATAGAAACAAT[C/T]AGAAAAACTGGCCAT | 25831 |
rs757308117 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147256 | GAGGCAGAGGTTGCA[A/G]TCAGCCGAGATCGCA | 25831 |
rs757321291 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194277 | AGGGACAGCACTAGA[A/T]GATGTTTCAAAGTGA | 25831 |
rs757326361 | snp | A/G | 1.65671e-05 | 0.00287807 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150212 | TAGCATCTTCCTGTG[A/G]TTCATCTTCCTAAAT | 25831 |
rs757330745 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158158 | TATTCCCATCATTAA[A/C]AAATTAGTATGCCTC | 25831 |
rs757332851 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171062 | CTCAATTTCTCTAAC[C/T]GTAAAAATAACTCCC | 25831 |
rs757342122 | in-del | -/GC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134568 | TGTGTGTGTGTGTGT[-/GC]GCGCGTATGTATATA | 25831 |
rs757357991 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137716 | CTGCACTCCAGCCTG[C/T]GCAACAGAGCTAGAC | 25831 |
rs757361288 | snp | C/T | 4.96866e-05 | 0.00498406 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178189 | GTCACCTCTAATACA[C/T]TGTCTGGAGCACTTT | 25831 |
rs757372096 | in-del | -/TCACTT | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208531 | CGTCCTACTGTACTC[-/TCACTT]TCAGCTTTTAAACAA | 25831 |
rs757393080 | snp | C/T | | | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133413 | TTCTTTAGCTGCTTT[C/T]CCTGTCAGGTAGAAA | 25831 |
rs757407150 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103139 | TACGATTCCAAAATA[C/T]CAAATTTCAAACCAA | 25831 |
rs757407794 | snp | A/C | 1.67888e-05 | 0.00289726 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144894 | ACGAGGCATGCTTTC[A/C]ACAGCTTTAAAATGG | 25831 |
rs757407943 | snp | C/T | 3.31285e-05 | 0.00406978 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168255 | AATAAAACCATATAA[C/T]TGGTGTAATTTGACT | 25831 |
rs757428544 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182978 | TACGTGGTATTTCCT[G/T]TAATACAGCCACTGA | 25831 |
rs757459876 | in-del | -/AA/CACAAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156549 | ACACACACACACACA[-/AA/CACAAA]AACAGATACATGTGT | 25831 |
rs757490348 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103951 | CAGCCTGGGAAACAA[A/G]AGCAAAAACTCCGTC | 25831 |
rs757535234 | snp | A/G | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157208 | TCCACTAGTATTGTA[A/G]GCAAATTGTGACCAA | 25831 |
rs757540462 | snp | A/G | 1.658e-05 | 0.00287919 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121443 | TAGCTGCGAGGTAAC[A/G]GCATGATGCGTTACA | 25831 |
rs757543352 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162427 | CCCCCTCCCCTGAAT[A/G]ATCTGAGAAACATCC | 25831 |
rs757576751 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174350 | AGGAGTTCAAGAACA[C/G]CCTGGCCAATATGGT | 25831 |
rs757578411 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31107895 | TCCACTTGTTGTACA[C/T]TATTACATGCTTAAG | 25831 |
rs757592979 | snp | A/G | 1.75265e-05 | 0.00296023 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129452 | CATCAATCCAGCCTG[A/G]AAAGGGACAGGAGTT | 25831 |
rs757599875 | snp | A/C | 1.66713e-05 | 0.0028871 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173572 | TTGAGAGCAGACTTA[A/C]AATTGTTGACACCTG | 25831 |
rs757621331 | in-del | -/AAAC | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163797 | GCCTGTAATCCCTGT[-/AAAC]AAACCCCTGGGAGGC | 25831 |
rs757633971 | snp | G/T | 4.97022e-05 | 0.00498484 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101228 | AGCCAGTCCACCTGG[G/T]GGTAGAGTTGAACAA | 25831 |
rs757643278 | in-del | -/ATC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144336 | ATCAGAACATCAATT[-/ATC]ATGACAATAATTTAG | 25831 |
rs757741681 | snp | G/T | 1.65655e-05 | 0.00287793 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116325 | TTGTACATAGTAAAA[G/T]ATGGTTGATCTGAAA | 25831 |
rs757756827 | snp | A/G/T | 4.97099e-05 | 0.00498527 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149034 | CCTTCTTTCAAACAT[A/G/T]TCAGTGACCAATTTC | 25831 |
rs757775414 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199940 | CTCTAAAATTTTTCT[C/T]TAATCCAGGCTTCAC | 25831 |
rs757815335 | in-del | -/A | 1.67654e-05 | 0.00289524 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172017 | TTCTATCCTTAATTT[-/A]AAATACCAGCTTTTA | 25831 |
rs757836295 | snp | A/C | 1.66682e-05 | 0.00288684 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139841 | AAGAAAAGTGTCACA[A/C]TGTTCCTAGATGCAT | 25831 |
rs757875508 | in-del | -/AAT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177513 | TGTCTCAAAAACAAT[-/AAT]AATAATAATAATAAT | 25831 |
rs757879599 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139589 | TGACTCATAATTGTA[C/G]AATAAGAGGAACCCT | 25831 |
rs757884677 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155050 | ACAAATTACTTATTA[A/C]AAAAGGAAAAAGAGG | 25831 |
rs757888708 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139352 | TCATGAATGGGATTA[C/G]TGTCCTTATAAAAGA | 25831 |
rs757901399 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138385 | ACAATTAAAGATTTA[C/T]ATGTGCATTTCGGTA | 25831 |
rs757923063 | snp | A/T | 6.64993e-05 | 0.00576587 | missense | HECTD1 | GRCh38.p7 | 14:31106945 | GAGTGAATCATGACC[A/T]TCTTCTGTAGAAGCT | 25831 |
rs757933751 | snp | A/G | 3.52175e-05 | 0.00419613 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149955 | TGAGAAAAAAACCAA[A/G]CTGTAGAAACTAGGA | 25831 |
rs757934979 | snp | C/T | 1.65655e-05 | 0.00287793 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116349 | TCTGAAATTGGTGAG[C/T]GGTAATTCAACTTCA | 25831 |
rs757955837 | snp | C/T | 8.32605e-05 | 0.00645161 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139848 | GTGTCACACTGTTCC[C/T]AGATGCATTCAGCAA | 25831 |
rs758012910 | in-del | -/GGTG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134562 | GTGTGTGTGTGTGTG[-/GGTG]TGTGTGCGCGCGTAT | 25831 |
rs758024349 | snp | C/T | 1.65704e-05 | 0.00287836 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127965 | ATGTAGTACCAGGTG[C/T]GGTCAAATTAGGGAA | 25831 |
rs758033243 | in-del | -/A | 1.66062e-05 | 0.00288146 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136480 | TTGTCCTAAAAGGCT[-/A]AAACCACAGCTCAGA | 25831 |
rs758051610 | snp | C/T | 3.31592e-05 | 0.00407167 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128645 | TCCTCCCCAAAGTAT[C/T]AGTGTTGTTATCACT | 25831 |
rs758056654 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132990 | CTAGGGGAAAAAACC[A/G]GAAGTGTGTCTTGAA | 25831 |
rs758069777 | snp | C/G | 1.65765e-05 | 0.00287888 | missense | HECTD1 | GRCh38.p7 | 14:31106733 | TTCTTCTCATCTTCA[C/G]AAAGACCTTTGTTGC | 25831 |
rs758086074 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178876 | AACCCTCCTTAAGCT[C/T]CCAAATACTTAAGTG | 25831 |
rs758111235 | snp | A/T | 1.67279e-05 | 0.002892 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171905 | CAGCATAATGTAATG[A/T]TGATGACCTTTGACC | 25831 |
rs758145219 | in-del | -/T | 0.000147365 | 0.00858258 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144969 | CACAACAAATGTGAA[-/T]TTTTTACAATTAATA | 25831 |
rs758190151 | snp | C/T | 1.65655e-05 | 0.00287793 | missense | HECTD1 | GRCh38.p7 | 14:31113318 | TCACTTGCAACTATA[C/T]ATAGAATACGCAGAA | 25831 |
rs758215664 | in-del | -/CACACA/CACACACA | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163079 | ACACACACACACACG[-/CACACA/CACACACA]CACACACACACACAC | 25831 |
rs758223211 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180891 | ACAAAACTGCCTAGC[A/G]TATCAGAATCTTAAG | 25831 |
rs758264526 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108479 | AAGTGATTGCATAAA[G/T]TATAATAAAAACTAC | 25831 |
rs758278492 | snp | A/G | 0.000137941 | 0.00830369 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106317 | TACCAACCAATTTTT[A/G]AGCTTTGCAAAGTGA | 25831 |
rs758289969 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131374 | GTTCAAATATATTTT[A/G]TAGATCAGTAACATT | 25831 |
rs758312884 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192473 | AAAATGAATGAAGCC[A/G]AAAGCTGGTTCTTGG | 25831 |
rs758329500 | snp | A/C | 0.000199339 | 0.00998147 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175088 | CACACAATTCAAACC[A/C]CCAGCCTCAAAGACT | 25831 |
rs758331578 | snp | C/T | 1.78236e-05 | 0.00298521 | missense | HECTD1 | GRCh38.p7 | 14:31113180 | GTAAACTGAAGCTGT[C/T]CATCACCATCTATAA | 25831 |
rs758352655 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111885 | CTCAGTGGGGCTGAG[A/G]CAGGAGAATCGCTTG | 25831 |
rs758404990 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204532 | ACTTGACTGACAAGT[A/G]TGATTTTTAAAATAC | 25831 |
rs758428010 | snp | A/C | 1.65633e-05 | 0.00287774 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128929 | ACACTGACAATTCCC[A/C]TGGATATTGCACTAG | 25831 |
rs758444446 | snp | G/T | 1.8233e-05 | 0.0030193 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107259 | CAAGATCAACCTAAT[G/T]TTTTAGAGGGTGAAA | 25831 |
rs758458910 | snp | C/T | 1.65641e-05 | 0.00287781 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205907 | CATCTGTAGCCATTC[C/T]AGCAATGTATCTGGG | 25831 |
rs758461982 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183206 | GAATTTGTTATATTT[C/T]ATTTAAAATATACAT | 25831 |
rs758463942 | snp | C/T | 3.6038e-05 | 0.00424473 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144064 | AGGAGTAACTACAAA[C/T]AATTTTTAAAACTGT | 25831 |
rs758470095 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144628 | TTGTTTTCAATCATT[C/T]AAAAGTATAAAAACC | 25831 |
rs758475505 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151004 | GAGAAGTTGAAGCAC[A/G]AAGACTGCCTGGGCC | 25831 |
rs758476628 | snp | C/T | 3.32303e-05 | 0.00407603 | missense | HECTD1 | GRCh38.p7 | 14:31107111 | TTGTCTTGAATGCAT[C/T]TGGCCAAGAAAATTC | 25831 |
rs758479061 | snp | C/T | 3.31378e-05 | 0.00407036 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148783 | TGCCAGTCCAGCCAG[C/T]CACAAATTCTGAACC | 25831 |
rs758494462 | snp | G/T | 3.31433e-05 | 0.0040707 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135610 | ATCATACCACTGTTT[G/T]GCTACCTAAACCAAA | 25831 |
rs758496464 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135870 | TAAAAATACAAAAAT[C/T]AGCCAGGCGTGGTGG | 25831 |
rs758497984 | snp | A/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208282 | GCAACCCTGGGAAAG[A/T]GGTGCTGCCGACGAT | 25831 |
rs758518381 | in-del | -/T | 0.000183355 | 0.00957308 | frameshift-variant | HECTD1 | GRCh38.p7 | 14:31113133 | ATATTTTTGTTGTAA[-/T]TTTTTTGCTAGTGAA | 25831 |
rs758523922 | snp | A/G | 5.00313e-05 | 0.00500131 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205761 | ACAGATGTCACTACA[A/G]TAACCCAAAGGAACA | 25831 |
rs758542399 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194460 | GCTAAAATGATACTT[C/G]TAGGCACAAAATTTT | 25831 |
rs758549202 | snp | A/C | 1.89016e-05 | 0.00307416 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135432 | AGAATTCTTTTACCA[A/C]GTGAATATGGTCACT | 25831 |
rs758597029 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183570 | ATCTGAAGTGAACAA[C/T]GTTAAATTCAGTCTT | 25831 |
rs758622564 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131569 | TGCAAGATGCTGCTA[A/G]TACAGGCACAAAGTA | 25831 |
rs758673675 | snp | C/G | 3.31741e-05 | 0.00407259 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31113923 | CTGTTTTTCCTAATA[C/G]TTTTATTAGTGCCAG | 25831 |
rs758675033 | snp | C/T | 1.90856e-05 | 0.00308908 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144980 | GTGAATTTTTACAAT[C/T]AATAATTTTACCAAA | 25831 |
rs758694746 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195434 | CGTTATAAAACACAA[C/T]GTCATACCCATAAAT | 25831 |
rs758697059 | snp | A/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164197 | TTATTTCCTGAACAG[A/T]TACTGTGCACAGGCC | 25831 |
rs758698296 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104017 | AGGTAAAGAAAAGAA[C/T]GGTATCAGAGGCTGG | 25831 |
rs758701568 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207967 | CTGCCGCGGCTTTTC[C/T]ATGGTGCGCCCTGGC | 25831 |
rs758741639 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162907 | ACCTTGTTTACACAC[A/G]AAAAAATAAAAAAAT | 25831 |
rs758774579 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125506 | CACAATCATCTTCAA[C/T]TTCCCATGACCAAGA | 25831 |
rs758778839 | snp | C/T | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157224 | GCAAATTGTGACCAA[C/T]ATCAGAATCACAAAC | 25831 |
rs758800109 | snp | G/T | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122984 | TCTTCATCTGGCTCA[G/T]GTAAGTCCTCATCAT | 25831 |
rs758800225 | snp | A/T | 1.67694e-05 | 0.00289558 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113507 | AACAATTAGAAAAAC[A/T]GGCCATTAATCACAT | 25831 |
rs758815065 | snp | C/T | 9.97009e-05 | 0.00705978 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136484 | TCCTAAAAGGCTAAA[C/T]CACAGCTCAGAATGC | 25831 |
rs758823884 | snp | C/T | 3.63299e-05 | 0.00426188 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129491 | CCAGCAGAAAGCAGA[C/T]AGGAGCGTGTCAGAC | 25831 |
rs758830368 | snp | C/G | 1.66729e-05 | 0.00288724 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173585 | TACAATTGTTGACAC[C/G]TGATTACTCAATTTG | 25831 |
rs758844632 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179372 | TGAAGTGAGCTGATA[C/T]TGCGCCACTGCACTC | 25831 |
rs758860113 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125461 | TACAGGCGTGAGCCA[C/T]AGCGCCCGGCCAGTT | 25831 |
rs758869068 | snp | A/G | 2.85335e-05 | 0.00377703 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109630 | TCTATGAGCTGCAGC[A/G]TACGTTAACAGCTGA | 25831 |
rs758874677 | snp | A/G | 3.43826e-05 | 0.0041461 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140025 | AATTATTATTAAGAG[A/G]TTTTGTATAACTACA | 25831 |
rs758930777 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151686 | TGAGCCACCGCGCCT[A/G]ACTCAGCATGTTTTT | 25831 |
rs758956415 | snp | C/G | 3.37285e-05 | 0.00410647 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173694 | CCAGCAGCAGCCATT[C/G]GAGATAACAGCTCCT | 25831 |
rs758974118 | in-del | -/AATGTGTAG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31150224 | TGGTTCATCTTCCTA[-/AATGTGTAG]AATGTGTAGAATTAT | 25831 |
rs759009884 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189823 | TGTCCACAACATTAT[C/G]TACCTCCCACCCCAC | 25831 |
rs759014471 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157649 | AACTACTAAGAAAAT[A/C]AATGGGGCCCAGTGC | 25831 |
rs759019571 | snp | C/T | 1.65875e-05 | 0.00287984 | missense | HECTD1 | GRCh38.p7 | 14:31100947 | AATTGAGATGAAAGC[C/T]TTTCTCCATTGTAGC | 25831 |
rs759039977 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181925 | TTTTTTGACAGTCTC[A/G]CTCTGTCACCCAGGC | 25831 |
rs759046262 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135758 | GGTGCGGTGGTTCAC[A/G]CCTGTAATCCCAGCA | 25831 |
rs759055562 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170880 | AACTTAATAAATTGT[C/T]CAAGATCATATAGCC | 25831 |
rs759071528 | snp | A/C | 1.67298e-05 | 0.00289217 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150260 | TAAACATGGAAAATA[A/C]TTTCAATTTCAAATA | 25831 |
rs759089229 | snp | C/T | 1.65776e-05 | 0.00287898 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136514 | CTTATTTCACCGTGC[C/T]CTTGCCAGAAACTCA | 25831 |
rs759096134 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194018 | AGCAGTTTAGGTCAT[-/A]AATCACCAAAACATC | 25831 |
rs759102597 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190634 | GCCAGACTGGAGTAG[C/G]ATGGCACAATTACAG | 25831 |
rs759105343 | snp | A/G | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173231 | GCTGCCGATGTGAGC[A/G]CTCCCCAGAACTATC | 25831 |
rs759106868 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159528 | TAGTTTTAGTAGAGA[C/T]GGAGTTTCATCATGT | 25831 |
rs759143205 | in-del | -/TG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31106058 | CTTTTAGGAAGAAAC[-/TG]TTGCTTTACTGAAGT | 25831 |
rs759166779 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170068 | CTGGCAATCAATGAC[A/G]TCGCCTCCTATATAC | 25831 |
rs759171480 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126833 | ACATCACACCTGGCT[A/G]ATTTTGGGGATGTAG | 25831 |
rs759181663 | snp | A/C | 1.66355e-05 | 0.002884 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119687 | GTATTAAAATTAAAT[A/C]ACAAAACCAAAACAT | 25831 |
rs759185434 | snp | A/C | 1.65605e-05 | 0.0028775 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129075 | TTGAGGGACGTTTTC[A/C]GCAGATGAAAGAACA | 25831 |
rs759231494 | in-del | -/TCAAGTATATGGG | 1.65622e-05 | 0.00287764 | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168356 | CTGGCAATAACCTTT[-/TCAAGTATATGGG]TGCCATTTCCGGATC | 25831 |
rs759243908 | snp | C/T | 3.31241e-05 | 0.00406952 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128990 | GGCCTAACTTCCTTT[C/T]AGCATTTTCACTTCC | 25831 |
rs759255262 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184397 | AGAGTTTGAGACCAG[G/T]CTGGACAACAAAGTG | 25831 |
rs759276303 | snp | A/C | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205858 | ATAGCTGTTCAAGGG[A/C]TATTAGTTGCATGTC | 25831 |
rs759296498 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31164822 | TAACCATCCAATAAG[A/G]GAACTCTGTTACATG | 25831 |
rs759298274 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196244 | TTGGACTTGTACTCC[A/G]GAATTTAAGTCATCC | 25831 |
rs759302388 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171305 | TAATCCCAGCCACTT[A/G]GGAGGCTGAGGCACG | 25831 |
rs759336398 | snp | A/G | 1.66785e-05 | 0.00288773 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135534 | AATCATGCTGGTGCC[A/G]AAATATAAAATTTTG | 25831 |
rs759356264 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195107 | TTTTGCCTCTGCTCC[C/T]AGCCTTGACTTTCTT | 25831 |
rs759369073 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148101 | TAGTCACCAGAAAAT[A/G]TTGACTCTAACTATG | 25831 |
rs759369572 | snp | A/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122965 | ATCTTCATTCTCATC[A/T]TCTTCTTCATCTGGC | 25831 |
rs759387905 | snp | A/T | 1.7765e-05 | 0.0029803 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144953 | GTACCTACCAAAATA[A/T]ACACAACAAATGTGA | 25831 |
rs759393501 | snp | A/G | 6.70365e-05 | 0.00578911 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148717 | GCACATCCAACAGAT[A/G]TACCTTTTGCTTTGT | 25831 |
rs759394569 | snp | C/T | 1.71355e-05 | 0.00292702 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113866 | AATAGTGTTTTGATG[C/T]CAATATATACCTTAT | 25831 |
rs759410835 | snp | G/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163955 | CCTCATAAAGATCTA[G/T]TTTGCTGCAAAGGAG | 25831 |
rs759418678 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199416 | TTTTTTTTTTTGAGA[A/C]AGAGTCTTGCTCTGT | 25831 |
rs759422014 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134453 | AGTATTATGTGATTA[C/T]ATGGAGAGTTTATGG | 25831 |
rs759425734 | in-del | -/A | 3.77031e-05 | 0.00434167 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174860 | AAACAGGGGAACACT[-/A]AAAAAAATCACTTTC | 25831 |
rs759468065 | snp | A/G | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168379 | ATGGGTGCCATTTCC[A/G]GATCTCCTTTGGGCT | 25831 |
rs759481246 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127437 | GCTCACTGTAACCTC[C/T]GCCTCCTGGGCTCAA | 25831 |
rs759488646 | snp | A/G | 3.76563e-05 | 0.00433898 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173765 | ACGACGGGTAAATCG[A/G]TCAGCCAGTGATGCA | 25831 |
rs759498422 | snp | A/G | 1.65715e-05 | 0.00287845 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139942 | AATGGAGAGGTAGAC[A/G]TTCAATAGATTCTAG | 25831 |
rs759519528 | snp | C/T | 1.65649e-05 | 0.00287788 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168250 | AGATAAATAAAACCA[C/T]ATAATTGGTGTAATT | 25831 |
rs759520379 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115891 | ATAAATTTACCCTAA[A/G]TCATTGATGATTATT | 25831 |
rs759533878 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207045 | AAGGGAAGTTCTGGA[A/G]AAGCAGCAGCAAGCC | 25831 |
rs759541834 | in-del | -/ACAAA | 8.66363e-05 | 0.00658108 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144020 | TTTAAATATTTCTTG[-/ACAAA]ACAAACTAAAAACCA | 25831 |
rs759549302 | snp | A/G | 0.00012499 | 0.00790438 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149165 | ACTTCGGCTTTCTAT[A/G]AAGACAAAATACTTG | 25831 |
rs759557992 | in-del | -/ATAGATA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188113 | TAGATAGATAGATAG[-/ATAGATA]GATAGATAGATAGAT | 25831 |
rs759568088 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187207 | CACAAAAAATCAAAT[C/T]AGCAAGGGGCAGTGG | 25831 |
rs759569086 | snp | A/G | 1.66045e-05 | 0.00288132 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105356 | AGTGAAAGGAGAGCA[A/G]TTATGCTAAAAATCC | 25831 |
rs759574206 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31107810 | ATCCAGTAATGTACC[-/T]TTTTTTCAAAATAGC | 25831 |
rs759576521 | snp | C/G | 1.65614e-05 | 0.00287757 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129266 | CAGATGTCTTGTCTG[C/G]ACAGTTGTTTTTCAC | 25831 |
rs759591148 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194186 | TACATGACATTCTAG[A/C]AAAGTCAAAACTATA | 25831 |
rs759595329 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181507 | GTGGTCCCAGCTACT[-/C]GGGAGGCTGAGGCAG | 25831 |
rs759617380 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31113045 | AAAGAAAGTAAAGGG[A/C]ATATTAGGAAAAGTC | 25831 |
rs759621871 | snp | G/T | 1.65622e-05 | 0.00287764 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31109418 | AACTGATTTCCGATC[G/T]GCATGTATTTGCATG | 25831 |
rs759631517 | in-del | -/G | 2.67262e-05 | 0.00365546 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133692 | TGTTAATATGTTAGA[-/G]AAAAAATTATGTAAT | 25831 |
rs759637076 | snp | C/G | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121260 | TTTCTTTGTGTAACT[C/G]TTTGGTAGCTCCCTC | 25831 |
rs759644161 | in-del | -/GT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190172 | GATTCTAGTGCCTAA[-/GT]GTCAAGTCACTTCCC | 25831 |
rs759677817 | snp | C/T | 1.65886e-05 | 0.00287993 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136703 | CTCTGGAAAACGTCT[C/T]GGTTTCTGTCTCAGA | 25831 |
rs759678284 | snp | A/C | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119443 | ACAGTAAAAATTTCC[A/C]ACCTTTAAATGGGAC | 25831 |
rs759720390 | snp | A/G | 1.65658e-05 | 0.00287795 | missense | HECTD1 | GRCh38.p7 | 14:31116303 | TACAGGACAATTGAA[A/G]CAATTTTTGTACATA | 25831 |
rs759747608 | snp | C/T | 1.65908e-05 | 0.00288012 | missense | HECTD1 | GRCh38.p7 | 14:31107593 | CATCATCTGGAAAAT[C/T]ATCATCACAAAGCCA | 25831 |
rs759755492 | snp | G/T | 1.70828e-05 | 0.00292252 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106625 | ATGCATTGGATTGAA[G/T]AATGTACATATAATG | 25831 |
rs759772192 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188526 | GGCGTGAGAAACCGC[A/G]CCCGGCCTTGTTATT | 25831 |
rs759772233 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167331 | GTCATGGTGGCATAC[C/T]TGTAGTCTCAGCTAT | 25831 |
rs759797154 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198376 | CAAAATTTAATCACG[G/T]ATGCCTTTCATTTCA | 25831 |
rs759798999 | snp | C/G | 2.62484e-05 | 0.00362264 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114382 | TCATATATAATTTGT[C/G]ATTATTTCCAATAAG | 25831 |
rs759801922 | snp | A/G | 1.65699e-05 | 0.00287831 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148975 | GTAAATCTTCTTTCA[A/G]TATTGTAGCTTGCTG | 25831 |
rs759830980 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191130 | GACCTGAGTCACTGC[A/G]CCTGGCCTCATTTTT | 25831 |
rs759870391 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117006 | CTAGAACAGAATACA[C/T]GTGTATGATAGAGAG | 25831 |
rs759893126 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145105 | GTTATTTGAGGAAAC[A/C]ACCTATGTATGTTCT | 25831 |
rs759966747 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143597 | GAATGTGACTCGAGC[A/G]CTACATTTCCATCCA | 25831 |
rs759970465 | snp | C/T | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100572 | ACAGCAACTGTAGTG[C/T]ATGGAGTATGAAATG | 25831 |
rs759991919 | snp | G/T | 0.000140657 | 0.00838502 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106179 | CATTAAAAAAAAAAG[G/T]CCTTGCAGTTAACCT | 25831 |
rs760010664 | snp | C/T | 1.65674e-05 | 0.00287809 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169375 | ACTGAAGAATAGCTA[C/T]CACTTCACTATGGCC | 25831 |
rs760018885 | snp | A/G | 1.74154e-05 | 0.00295083 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175158 | AATAGTAAAACAAAT[A/G]TAACGAAAGAATGCA | 25831 |
rs760028063 | snp | A/G | 1.78592e-05 | 0.00298819 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144172 | ATTTCATATGGTGAA[A/G]TTGTGTTTTCATCCT | 25831 |
rs760078130 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111845 | ATTAGCCACGCGTGG[C/T]GGCGTGCACCTGTAA | 25831 |
rs760079592 | snp | A/C | 1.67379e-05 | 0.00289287 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133450 | AAATAAAAACCAAAT[A/C]ACTTTTTACAAAAGT | 25831 |
rs760107123 | snp | C/T | 1.65696e-05 | 0.00287828 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175033 | CAGAGTGCAAGGTGT[C/T]TTTATGAACTAGATG | 25831 |
rs760118300 | in-del | -/AAAAAAT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204620 | GAGTCAGGATGAGGA[-/AAAAAAT]AAAAAATAAAAATAA | 25831 |
rs760119619 | snp | A/G | 1.80169e-05 | 0.00300135 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144196 | TCATCCTTCAAAAGT[A/G]CAATTAGGTTTTCTA | 25831 |
rs760132364 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205447 | CATAAATCAATTTCA[C/T]GGTACAGAAATAGAT | 25831 |
rs760132871 | snp | G/T | 1.68298e-05 | 0.00290079 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156861 | TGGTTTTGATTCCTC[G/T]TCATTCTCATCATCA | 25831 |
rs760140425 | snp | C/T | 5.68241e-05 | 0.00532999 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133671 | GAGGCCAAGTTGCAG[C/T]TGACCTGTTAATATG | 25831 |
rs760183732 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192833 | ACGCAAAAAATTAGC[C/T]GGGTGTGGTGACAGG | 25831 |
rs760191089 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207213 | GGCCCCGCCGCCGGC[A/G]GGGCCCCGGGAGGGG | 25831 |
rs760259504 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145250 | GCAACAGAAAAAAAC[A/G]TATCTCTCTAAACTA | 25831 |
rs760262209 | in-del | -/ACA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142772 | AGTGCATCAGCACAT[-/ACA]ATGATTAAGATCAAG | 25831 |
rs760305544 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159596 | CTGCCTGCCTCAGCC[G/T]CCAAAGCGCTGGGAT | 25831 |
rs760321017 | in-del | -/ATAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176422 | TTAATTTATTTTAAG[-/ATAA]ATAAATACTTTAAAT | 25831 |
rs760327911 | snp | A/G | 1.91375e-05 | 0.00309328 | stop-gained | HECTD1 | GRCh38.p7 | 14:31113112 | TTATTACCTCAATCT[A/G]CTGTAATATTTTTGT | 25831 |
rs760329506 | snp | G/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121438 | TGTGGTAGCTGCGAG[G/T]TAACAGCATGATGCG | 25831 |
rs760329878 | snp | C/G | 1.65976e-05 | 0.00288072 | missense, nc-transcript-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121388 | AAGATATTACCTGCT[C/G]CCCAATAGGTCGGCT | 25831 |
rs760329935 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153198 | GAGATCGAGACCATC[A/C]TGGCTAACACGGTAA | 25831 |
rs760344880 | snp | C/G | 1.65718e-05 | 0.00287848 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101129 | TTCTTTCTTTCAAAA[C/G]TAAAGTAACTAAATT | 25831 |
rs760363468 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204254 | TTATAATCCTTTGGG[A/T]ATATACCCAGTAATG | 25831 |
rs760375143 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166904 | ACAGGTGCATGCAGA[A/G]GCTCACACTTACAAT | 25831 |
rs760407612 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112123 | TCCCTTAATGTCTAC[A/G]GTATCACCTCTCTTT | 25831 |
rs760439480 | in-del | -/ATTAA | 1.83098e-05 | 0.00302565 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178289 | ATTACATCTAGGGTT[-/ATTAA]ATTCTTAACAGCAAA | 25831 |
rs760453360 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196004 | GCTGTCTGTTTACAG[A/G]AATTCATTTAACTTT | 25831 |
rs760454073 | snp | A/C/G | 3.32454e-05 | 0.00407698 | missense, synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107567 | GAGAAATATTCTTAC[A/C/G]TGACGAGATTCATCA | 25831 |
rs760461743 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152293 | ATTCAAAGAAATCAC[A/C]AATTTGGGATCATAG | 25831 |
rs760487791 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103882 | TGAAGCAGGAAAATC[A/G]CCTGAACCCAGGAGG | 25831 |
rs760501818 | snp | C/T | 1.66932e-05 | 0.002889 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31114047 | GCTCCACATGCTCTA[C/T]AGACCAGCAACCCTA | 25831 |
rs760515240 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135847 | ACATGGTGAAACCCC[A/G]TTTCTACTAAAAATA | 25831 |
rs760524201 | snp | C/T | 1.65784e-05 | 0.00287905 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135580 | TCGAACAAAAACAAA[C/T]GAAGATCGGTCAAAA | 25831 |
rs760525030 | snp | A/G | 5.0463e-05 | 0.00502284 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107224 | CTGCACATAATATCC[A/G]GGAGGTTTCAATCCA | 25831 |
rs760527902 | in-del | -/TATC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151105 | TCTATTATCTATATC[-/TATC]TATCTATCTATCTAT | 25831 |
rs760531445 | snp | A/G | 3.31329e-05 | 0.00407005 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136542 | TCACCATTTTCAAAA[A/G]GTACTGTTCCAGAGA | 25831 |
rs760552395 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170980 | ACCAAATAACTTCAC[A/G]ATTGGCAGATTACAG | 25831 |
rs760553341 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31150497 | TCCCAAGTAGCTGGG[A/G]TTACAGGTCCAAGCC | 25831 |
rs760570161 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122541 | AGTGCAGTGATGCAA[G/T]TATAGCTCACTGCAG | 25831 |
rs760580603 | snp | C/T | 4.4154e-05 | 0.00469841 | missense | HECTD1 | GRCh38.p7 | 14:31114330 | AATCCTTCATTTCTC[C/T]GTACATGATTCTAAA | 25831 |
rs760580950 | in-del | -/TGTGTGTG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134525 | ATGCATAAATGTGTG[-/TGTGTGTG]TGTGTGTGTGTGTGT | 25831 |
rs760630571 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118353 | TTAATCAACAATTTA[A/G]ATCTTTGTTAAGGAT | 25831 |
rs760647479 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194267 | TTGAGTTCAAAGGGA[C/T]AGCACTAGATGATGT | 25831 |
rs760651076 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189573 | CAAGACCAGCCTGGG[C/T]AACATAGCGAGATCC | 25831 |
rs760651546 | snp | C/T | 3.48292e-05 | 0.00417294 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168523 | GGAAACTTTTGCTTT[C/T]AAGGAAAAAAACCTT | 25831 |
rs760651756 | snp | C/T | 1.65954e-05 | 0.00288053 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148737 | TTTTGCTTTGTTTTT[C/T]CTAACTTAGATTTCA | 25831 |
rs760672938 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205890 | CTTTCATCTCCCTGT[C/T]CCATCTGTAGCCATT | 25831 |
rs760702417 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124414 | GGTAAGAGAAAAACC[A/G]CAAAACACAGTAAAA | 25831 |
rs760718823 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125988 | TATCCTAAGGAAGTA[C/T]ATTAAAATACAGTTC | 25831 |
rs760719843 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174218 | TTATTTTCTAAAGTA[C/T]GCTAATTCAATAAGG | 25831 |
rs760759321 | snp | A/T | 1.66613e-05 | 0.00288623 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121520 | TCTAAAATAAAACAA[A/T]CCCAAGAGATACATG | 25831 |
rs760773375 | snp | A/G | 1.6585e-05 | 0.00287962 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31103034 | GGCTGAAGGAACTTA[A/G]TTTCTCCATTGGAAA | 25831 |
rs760778778 | snp | A/C | 6.62427e-05 | 0.00575473 | missense | HECTD1 | GRCh38.p7 | 14:31109452 | TTCTCAGCCCATTCC[A/C]TCAGTGACTCGCCAC | 25831 |
rs760814555 | snp | A/T | 3.41857e-05 | 0.00413421 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129426 | GTTTGAGCCACCAGC[A/T]TCCCAGGTGACATCA | 25831 |
rs760844570 | snp | A/C/G | 6.86253e-05 | 0.00585738 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141849 | ATTCAAAGAAATTTG[A/C/G]GATTTTACCTTTCAT | 25831 |
rs760876779 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200605 | GCCAACATAGTGAAA[C/T]CCGATCTCTACTTAA | 25831 |
rs760910848 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31107905 | GTACACTATTACATG[C/T]TTAAGCACTGTGCCA | 25831 |
rs760922784 | snp | A/G | 3.3189e-05 | 0.0040735 | missense | HECTD1 | GRCh38.p7 | 14:31116419 | AATCGAGGTGACGGA[A/G]TACATTCGACTTCTT | 25831 |
rs760924377 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155669 | GCTGTAGGTTCTCAG[A/G]ACAAACTATCGCAGG | 25831 |
rs760926321 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139393 | ATCTTGTTCATCCCT[G/T]CTACAATGTGAGAAC | 25831 |
rs760967374 | snp | A/T | 1.65737e-05 | 0.00287864 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139964 | AGATTCTAGTACAGC[A/T]ATTAACTTTCGAATT | 25831 |
rs760972987 | snp | C/T | 0.000100629 | 0.00709256 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171987 | AACGAATCATAAAGC[C/T]GCTTTTTATTAATAT | 25831 |
rs760978985 | snp | C/G | 1.65773e-05 | 0.00287895 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128782 | GGTACACTTGCACTA[C/G]AGCTCATAGGGGCCC | 25831 |
rs760995887 | snp | C/T | 1.65875e-05 | 0.00287984 | missense | HECTD1 | GRCh38.p7 | 14:31106770 | TTTGGCGCCTCTTGA[C/T]AGCAAGGTCTTTAAT | 25831 |
rs761020984 | snp | A/C | 4.53289e-05 | 0.0047605 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149177 | TATAAAGACAAAATA[A/C]TTGTTTCAAAATCTT | 25831 |
rs761022860 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159773 | GCCTCCCAAATAGCT[C/T]GGACTACAGGCTCCT | 25831 |
rs761026323 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188670 | ATTGTAACTCTCTCC[C/T]AAAAGCTCCTCAGGA | 25831 |
rs761031726 | snp | G/T | 1.65718e-05 | 0.00287848 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128053 | ATAGGTGAGATTGTA[G/T]AAACCTCAGAAAAAC | 25831 |
rs761051523 | in-del | -/A | 0.000237883 | 0.0109034 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112397 | TTATTCTAAAAACAT[-/A]AAAAAAAAGGCTTCT | 25831 |
rs761079916 | snp | A/G | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178051 | GCTAAGTCTCTGCTA[A/G]TCCTGTTGTTAAGTT | 25831 |
rs761099712 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204437 | TGACTTTTTAATGAT[-/C]GGGCAACACTTTTTT | 25831 |
rs761107254 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130847 | CCTCTATTTTTTTCT[A/G]TATGCTGAAATAATC | 25831 |
rs761118273 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199531 | ATCAGCCTGGCCAAC[A/G]TGGTGAAACTCCGTC | 25831 |
rs761151626 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180299 | TTAGGGCCCGTATGG[C/T]GGCTCACACTTGCAG | 25831 |
rs761154685 | snp | A/G | 1.65765e-05 | 0.00287888 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134911 | TCAACATGGGTATAC[A/G]AAGAAGTCCAGTTCT | 25831 |
rs761162594 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124099 | CTTAAATTTGATAAA[A/G]TATGTTACCCTTTAA | 25831 |
rs761179589 | snp | A/C | 2.84645e-05 | 0.00377246 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171824 | TTTTAAACCATGTAA[A/C]TGTTAAAAATTAGTA | 25831 |
rs761193041 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190761 | TCCTGGGCTCAAGCA[A/G]TCCTCCCACCTTGGC | 25831 |
rs761231473 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101771 | CATTCCAGCCTGGAC[A/C]ATAAGAGCGAAACTC | 25831 |
rs761239314 | snp | A/C | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134951 | TGGATACCTGGAAAA[A/C]CCAATTTCTCAGTGC | 25831 |
rs761243921 | in-del | -/TCT | 1.65688e-05 | 0.00287821 | cds-indel, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119856 | CCTTTAGTTTCGTAC[-/TCT]TCTTCTTCCTATCAA | 25831 |
rs761255130 | snp | C/T | 1.78302e-05 | 0.00298577 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175172 | TGTAACGAAAGAATG[C/T]AAGCCTGATTTTCAA | 25831 |
rs761275772 | snp | C/T | 1.6821e-05 | 0.00290004 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106639 | AGAATGTACATATAA[C/T]GCTTACCCTAAATCC | 25831 |
rs761284384 | snp | C/T | 1.65633e-05 | 0.00287774 | missense | HECTD1 | GRCh38.p7 | 14:31113403 | GAGGTTGTTCTTTTG[C/T]TAAATTAAGAATATC | 25831 |
rs761330361 | in-del | -/AAT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177511 | AACTGTCTCAAAAAC[-/AAT]AATAATAATAATAAT | 25831 |
rs761333051 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193983 | CTCACACACACACAA[A/T]ATCTATACACTACTG | 25831 |
rs761333547 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31113202 | CATCTATAAAATTAA[G/T]TAATAAAATTAATAA | 25831 |
rs761338082 | snp | C/T | 1.66081e-05 | 0.00288163 | missense | HECTD1 | GRCh38.p7 | 14:31106806 | TTAAAAATCTGGCTC[C/T]GTGTGGGTTTACTAA | 25831 |
rs761405952 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146599 | ACATATCAGGCTGGG[C/T]GCAGTGGCTTTTGGG | 25831 |
rs761484760 | snp | C/T | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121332 | GTTGGTGCTTTACTA[C/T]AAAAGGGAAAAATAT | 25831 |
rs761543372 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114523 | TTTTGCTATGTTGTC[C/T]AGGCTAGTTTCAAAC | 25831 |
rs761548137 | snp | G/T | | | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173657 | TGGTTTGCATGCTGA[G/T]GATGGTCCTGAAACA | 25831 |
rs761548619 | snp | G/T | 5.01609e-05 | 0.00500779 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144817 | CATACTTGTCTATTT[G/T]TATGAAGTTCCCAAG | 25831 |
rs761550936 | snp | C/T | 4.97244e-05 | 0.00498596 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129373 | TACCCTGGTGCAAGC[C/T]TGAGGTCAAATTTTC | 25831 |
rs761562182 | snp | C/T | 1.65701e-05 | 0.00287833 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101162 | ATTTGGATTCCCCAT[C/T]AGCCAGAGAGCTTGT | 25831 |
rs761581809 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139178 | CCGAAAAAAATTGTG[C/T]TTAAAATATCTTGAC | 25831 |
rs761596142 | snp | A/G | 3.31246e-05 | 0.00406955 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129254 | AGCCTGCAGCAGCAG[A/G]TGTCTTGTCTGGACA | 25831 |
rs761603788 | snp | A/G | 6.65646e-05 | 0.0057687 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157127 | AGACTACTAGCTAAA[A/G]GAAATTAATGCTAAA | 25831 |
rs761649693 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31172249 | GAGCCAAGAGAGTGT[G/T]TTAAATATTTAGGTC | 25831 |
rs761671405 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137622 | ATGCATGCCTGTAGT[C/T]CCAGGTATTGGAGAG | 25831 |
rs761694885 | snp | A/T | 1.65729e-05 | 0.00287857 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148958 | TTCAAATACAAAACC[A/T]GGTAAATCTTCTTTC | 25831 |
rs761710955 | snp | A/C | 1.67472e-05 | 0.00289367 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173514 | AAGCAAAGATTCAAA[A/C]ACATTCTTACATGTG | 25831 |
rs761713038 | snp | C/G | 1.6569e-05 | 0.00287824 | missense | HECTD1 | GRCh38.p7 | 14:31109399 | TATATGAGATTACCT[C/G]AAGAACTGATTTCCG | 25831 |
rs761722620 | snp | C/G | 1.65809e-05 | 0.00287926 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136693 | GATCAAAATACTCTG[C/G]AAAACGTCTTGGTTT | 25831 |
rs761722875 | snp | A/C | 1.65611e-05 | 0.00287755 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129151 | ATTACAATTTCTGAT[A/C]TCCGTTCCGTTTTGG | 25831 |
rs761728563 | snp | A/G | 1.65784e-05 | 0.00287905 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156948 | ATCCAAAAATATATC[A/G]CCACCTTTATCTACT | 25831 |
rs761739579 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154093 | TTCCAGGTTGCTTTG[C/G]CTATTACATTTATAT | 25831 |
rs761745907 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147017 | AATAACTTTATAAAA[C/T]GTAACTACTGTTGGC | 25831 |
rs761748066 | snp | A/T | 1.6701e-05 | 0.00288968 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123094 | CACAATTAAGAAAGC[A/T]TAACAAAGGAACTTT | 25831 |
rs761770594 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143275 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGGTGCCT | 25831 |
rs761775793 | snp | C/G | 1.65619e-05 | 0.00287762 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136628 | GCAGTTTCACCAGGT[C/G]CACGTTCCAACCGAA | 25831 |
rs761782257 | in-del | -/A | 0.000232219 | 0.0107729 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144265 | TCAATACACTAAAAG[-/A]AAAAAAAATTTAATG | 25831 |
rs761814432 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105965 | AACCACCTTTCTATA[G/T]TTTACTTCTAACTTA | 25831 |
rs761832448 | snp | C/G | 4.96915e-05 | 0.0049843 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173389 | TCACCCTGCAATGCA[C/G]TTTCAATTGAATCTG | 25831 |
rs761837438 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31119032 | ATCTGTTTCCTTGCC[-/T]TTTTCTAGCATCTAG | 25831 |
rs761858434 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31113870 | GTGTTTTGATGCCAA[C/T]ATATACCTTATATGC | 25831 |
rs761897521 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112960 | TAAACCTGTAATTAG[A/G]AAATAAATGCAAAGG | 25831 |
rs761908738 | snp | C/G/T | 3.31242e-05 | 0.00406955 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168383 | GTGCCATTTCCGGAT[C/G/T]TCCTTTGGGCTCATT | 25831 |
rs761914625 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31164894 | ACTTATACTCCAGAA[C/T]GATTCTTGCACTGGC | 25831 |
rs761923439 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110849 | TTGGCCAGGCTGGTC[A/T]CGAACTCCTGGCCTC | 25831 |
rs761950733 | snp | C/G | 1.67798e-05 | 0.00289648 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173682 | GAAACAGTACCACCA[C/G]CAGCAGCCATTCGAG | 25831 |
rs761958478 | snp | C/T | 3.3123e-05 | 0.00406945 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122971 | ATTCTCATCATCTTC[C/T]TCATCTGGCTCAGGT | 25831 |
rs761971459 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127536 | TTCTTTTGTATTTTT[A/G]GTAGAAATGGGGTTT | 25831 |
rs761974972 | snp | C/T | 1.67175e-05 | 0.0028911 | missense | HECTD1 | GRCh38.p7 | 14:31103066 | ACTTTATTAAACCCA[C/T]CTACATCGTACATGT | 25831 |
rs761985708 | snp | A/G | 1.66098e-05 | 0.00288177 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133379 | CTAGACGTCTCTGCC[A/G]TCTAAGATTAGCTTC | 25831 |
rs762003350 | snp | A/G | 4.97179e-05 | 0.00498562 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31105390 | AAAATTACCTCTAAA[A/G]GCTTCCATTTGTTTC | 25831 |
rs762035566 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183122 | AAGCAAGAAATTTGA[C/T]GTAAAACTCAGTAAC | 25831 |
rs762056004 | snp | C/T | 1.65831e-05 | 0.00287945 | missense | HECTD1 | GRCh38.p7 | 14:31112459 | AATAAAGCTGTCTAG[C/T]TTCAAATGGTATTAG | 25831 |
rs762056745 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155713 | GATAAGCAATGTAAT[A/G]TGTGCTCCTGGATTT | 25831 |
rs762081142 | snp | C/T | 2.76882e-05 | 0.00372066 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141970 | AAAGAAAACAAAAAG[C/T]ATAAAGTCCAAAAAA | 25831 |
rs762086563 | snp | A/G | 1.98155e-05 | 0.0031476 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173778 | CGGTCAGCCAGTGAT[A/G]CAAAGCATCGCAGAG | 25831 |
rs762100268 | in-del | -/A | 1.68371e-05 | 0.00290143 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112578 | ATGTCTTAGTGCTAT[-/A]AAGGCATTCATGCAT | 25831 |
rs762102121 | snp | A/G | 1.65619e-05 | 0.00287762 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150087 | GAACCATCCATTACT[A/G]CCATTAGATAATTCC | 25831 |
rs762111427 | snp | C/T | 2.23826e-05 | 0.00334527 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109605 | ACTATTGCTCTGAAA[C/T]AGAAAAATATCTATG | 25831 |
rs762111581 | snp | C/G | 1.66757e-05 | 0.00288749 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119668 | TTCATATCTGATTTA[C/G]TATGTATTAAAATTA | 25831 |
rs762112462 | snp | G/T | 1.66344e-05 | 0.0028839 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133277 | TGCCTTCTCCCTGTG[G/T]GCTGCCATCCTGATC | 25831 |
rs762160321 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175267 | AAATGAAATTAATTT[A/T]AATAATACATTTTAG | 25831 |
rs762165815 | snp | C/T | 3.23965e-05 | 0.00402458 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141855 | AGAAATTTGAGATTT[C/T]ACCTTTCATCATCTT | 25831 |
rs762169306 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185400 | TTAGGGAATTTCATA[C/G]CATCATTTTCAGAGA | 25831 |
rs762224704 | snp | A/G/T | 0.000129546 | 0.0080472 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172152 | GAAAAAAAAAGAAAC[A/G/T]TATTTTTAAAGCCAA | 25831 |
rs762225117 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200745 | CAGATCACGCTATTA[C/T]ACTCCAGCATGGGTG | 25831 |
rs762225923 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31109044 | CTCCCAAAATATCAA[A/T]CAGCACAGTTTAATG | 25831 |
rs762236240 | snp | C/T | 4.98625e-05 | 0.00499287 | missense | HECTD1 | GRCh38.p7 | 14:31116434 | GTACATTCGACTTCT[C/T]CCAAGAGCTCTGAAT | 25831 |
rs762261562 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31121980 | AAATTTTTTTTTTTT[-/A]ATGCCTCTACTTCAT | 25831 |
rs762287722 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31168700 | TACTCCACTTCGTTC[C/T]AAAAATTATTTCACA | 25831 |
rs762292231 | in-del | -/A | 1.66776e-05 | 0.00288765 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121333 | TTGGTGCTTTACTAT[-/A]AAAGGGAAAAATATA | 25831 |
rs762311441 | snp | G/T | 1.66358e-05 | 0.00288402 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149204 | TCTTATTTCTTTCAA[G/T]TATGACATGTATTTT | 25831 |
rs762313857 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108131 | AGTTTCACTCTTGTC[A/G]CCCAGGATGGAGTGC | 25831 |
rs762316556 | snp | A/G | 1.6696e-05 | 0.00288924 | missense | HECTD1 | GRCh38.p7 | 14:31116453 | AGAGCTCTGAATGAG[A/G]GGTCCCTAAAAATTT | 25831 |
rs762326061 | snp | C/T | 5.06881e-05 | 0.00503403 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178258 | CGAGGAGGACATCTG[C/T]AGTGAAAGAAATCAT | 25831 |
rs762356374 | snp | G/T | 3.31461e-05 | 0.00407086 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128820 | CAACAAAGAACTCAC[G/T]GACAGTCTGTTACTT | 25831 |
rs762378038 | snp | C/T | 1.65696e-05 | 0.00287828 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128846 | TACTTGCTGAAGAGC[C/T]AAGAGGTCGTTGTGA | 25831 |
rs762432356 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31168926 | GCGGGTGCCTGTAGT[C/T]CCAGCTACTAGGGAG | 25831 |
rs762436284 | snp | C/T | 3.36101e-05 | 0.00409926 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172000 | GCTGCTTTTTATTAA[C/T]ATTTCTATCCTTAAT | 25831 |
rs762456191 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199610 | ATCCCAGCTACTAGG[A/G]AGGCTGATGCTGGAG | 25831 |
rs762479037 | snp | A/G | 1.65627e-05 | 0.00287769 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128965 | CCAGGAGTACGAACA[A/G]AACTATCAGGGCCTA | 25831 |
rs762507485 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184054 | ACATATTATTCAAGT[A/G]AAAATAGATGTAATC | 25831 |
rs762522878 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127018 | GCTTTGTCGCCCAGG[C/T]TGAAGTGCAGTGGTG | 25831 |
rs762560439 | snp | C/T | 1.75823e-05 | 0.00296493 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135480 | GACTGACTTACTTTG[C/T]ATTTGTTCCAATCCA | 25831 |
rs762626779 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174786 | AAAATTAGAGAAAGA[A/G]GATGGAATTACCTCG | 25831 |
rs762667444 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194072 | AACTAAAGAGAATGA[A/G]CTATTGACACAATAG | 25831 |
rs762675084 | snp | C/T | 9.93624e-05 | 0.00704779 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178143 | GGTACATTCCGCAGA[C/T]ACATCCAGGTAGTAT | 25831 |
rs762732770 | snp | C/T | 1.65781e-05 | 0.00287902 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157168 | AAAGAAACGGACCTC[C/T]TGATCCAGGACAGTT | 25831 |
rs762737350 | snp | C/T | 3.43962e-05 | 0.00414691 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144937 | TCTCGAGCCATAGTT[C/T]GTACCTACCAAAATA | 25831 |
rs762748615 | snp | C/T | 1.65674e-05 | 0.00287809 | missense | HECTD1 | GRCh38.p7 | 14:31113423 | TTAAGAATATCACTA[C/T]TTTGAAGAGTAGAAA | 25831 |
rs762773532 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162140 | GGGAGGCTGAGGCAC[A/G]AGAATCGCTTGAACC | 25831 |
rs762797537 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114612 | TCACGACACCCAGCC[A/T]CAAGGAGTATTTTTA | 25831 |
rs762801335 | snp | C/T | 1.65866e-05 | 0.00287976 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121491 | TCGACGTTGCAGGGA[C/T]GGGCGTCTCAGAATC | 25831 |
rs762813133 | snp | C/T | 1.67167e-05 | 0.00289103 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173530 | ACATTCTTACATGTG[C/T]TACTACCGGAGAGCC | 25831 |
rs762858512 | snp | C/T | 1.67036e-05 | 0.0028899 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129395 | CAAATTTTCCTTCTG[C/T]GCCCATACGGTAAGA | 25831 |
rs762860849 | snp | C/T | 1.66726e-05 | 0.00288722 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144852 | CTCTAACTGAGTTGC[C/T]ATGTTTCTGAGTGTT | 25831 |
rs762862754 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146768 | TGAGGCAGGTGAATC[A/G]GTTGAACCTGGAAGG | 25831 |
rs762882051 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171535 | CTAGGTGACTAGTTG[A/G]ATAAACTTGTAGTAC | 25831 |
rs762885518 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31113569 | TACCACTATGAAAGG[C/G]TTGGAATTTTTTAAA | 25831 |
rs762893405 | snp | C/T | 3.31307e-05 | 0.00406992 | missense | HECTD1 | GRCh38.p7 | 14:31103001 | GGTTTCCACAAAGAA[C/T]CATTTGGACTTCTTC | 25831 |
rs762907262 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165910 | GAATGCAGTGGCGCA[A/G]TCTTGGCTCACTGCA | 25831 |
rs762916058 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202960 | CAGGTATGGTGGCAC[A/G]CACCTGTTGTCCCAG | 25831 |
rs762963034 | in-del | -/C | 1.6755e-05 | 0.00289435 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173510 | TAAAAAGCAAAGATT[-/C]AAAAACATTCTTACA | 25831 |
rs762964266 | snp | C/T | 3.35149e-05 | 0.00409345 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169504 | ATTTGAATATAACAA[C/T]ACTTTATTTCTTTGA | 25831 |
rs762971355 | in-del | -/TG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122381 | GTGTGTGCGCGCATG[-/TG]TGTGTGTGTGTGTGT | 25831 |
rs763002703 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31173855 | TCCACCTAAAAAGGG[A/T]TAGTAATGATCATTT | 25831 |
rs763003455 | snp | A/G | 1.69789e-05 | 0.00291362 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101347 | AACAAAAATATAGTT[A/G]TATTGAGTTGACTGC | 25831 |
rs763008733 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177535 | AATAATAATAATAAT[-/A]CTATTCCTGGCACCA | 25831 |
rs763015089 | in-del | -/CT | 1.95139e-05 | 0.00312355 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156805 | AAAAAAAAAAAAAAA[-/CT]CTTCCTGATACCTCT | 25831 |
rs763017912 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163404 | GCCAAGATTGTGCCA[C/T]TGCACTCTAGCCTAG | 25831 |
rs763030767 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198243 | CATACGGAAGAATAA[C/T]GGCAAAGTACATACT | 25831 |
rs763032139 | snp | C/T | 3.31214e-05 | 0.00406935 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205865 | TTCAAGGGCTATTAG[C/T]TGCATGTCCCTTTCA | 25831 |
rs763105553 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137507 | CTGAGGCAAGAGGAT[C/T]AATTGCTTGTGCCTA | 25831 |
rs763114785 | snp | C/T | 1.65999e-05 | 0.00288091 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148861 | TAACATATTCATTTA[C/T]TTGTACCCAATAAAC | 25831 |
rs763127665 | snp | C/T | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100392 | ATAAAAAGTTTGGTG[C/T]ATGATTATATGCCAA | 25831 |
rs763152957 | in-del | -/TCA | 1.65611e-05 | 0.00287755 | cds-indel, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122960 | TTGTCATCTTCATTC[-/TCA]TCATCTTCTTCATCT | 25831 |
rs763165992 | snp | A/C | 1.66313e-05 | 0.00288364 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169330 | AACAGTAGATGGCTT[A/C]AAAAGAAAGAATGTA | 25831 |
rs763183785 | snp | G/T | 3.3335e-05 | 0.00408245 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133417 | TTAGCTGCTTTCCCT[G/T]TCAGGTAGAAATTGG | 25831 |
rs763187090 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117808 | AAATATACTGGCAGA[A/G]AGCTCTACAAAAAGT | 25831 |
rs763189183 | snp | C/T | 1.72478e-05 | 0.00293659 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114080 | ACAGGAAAAACCAAA[C/T]GTTGGCCTTTCCCAA | 25831 |
rs763192596 | snp | A/C/T | 6.62493e-05 | 0.00575502 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129241 | TTTCTACTTGAGGAG[A/C/T]CTGCAGCAGCAGATG | 25831 |
rs763195575 | snp | A/G | 1.65636e-05 | 0.00287776 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127898 | AAAACTGTTGTTGCT[A/G]TAGCTACATTGCTGC | 25831 |
rs763210903 | in-del | -/T | 0.000267664 | 0.0115655 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133464 | CACTTTTTACAAAAG[-/T]TAATTGTTTTAGTAA | 25831 |
rs763217492 | snp | C/T | 1.65902e-05 | 0.00288008 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133539 | ATACTCCATTTACAG[C/T]GCCATAAAGTTCGAA | 25831 |
rs763221779 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141811 | AGGAAGTATACCAAC[G/T]GTGTGAACATTACAA | 25831 |
rs763236550 | snp | C/T | 1.65647e-05 | 0.00287786 | missense | HECTD1 | GRCh38.p7 | 14:31105424 | ATACCCGTATGCATA[C/T]AAAAGTCAAACATCA | 25831 |
rs763236645 | snp | A/G | 2.08635e-05 | 0.00322976 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113054 | AAAGGGAATATTAGG[A/G]AAAGTCCAACAGTAA | 25831 |
rs763238372 | snp | A/T | 3.61448e-05 | 0.00425101 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141986 | ATAAAGTCCAAAAAA[A/T]AATAATTTAAGGATC | 25831 |
rs763277846 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153891 | AATTATTTTGCATAT[C/G]CTATTGGCTTGTTCA | 25831 |
rs763283377 | snp | A/T | 3.31246e-05 | 0.00406955 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119811 | TGTCTCTTTAGCACA[A/T]AATCATCATCCCATG | 25831 |
rs763296090 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159107 | AAAGAGGCAAAATTT[A/T]CAACTGATGTCCTAG | 25831 |
rs763297250 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165196 | TCTTATAAAACTGCC[C/T]GCTCTACAGACCTCC | 25831 |
rs763317817 | in-del | -/TATC | 6.62581e-05 | 0.0057554 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105498 | AAGAAAATTTGTCAG[-/TATC]TAGGAATATTTCAGG | 25831 |
rs763318974 | in-del | -/AAATC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31106489 | TGTCTTTATAATATT[-/AAATC]AAAGGTTCAAGTCGA | 25831 |
rs763329599 | snp | A/G | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178133 | CAATCCTTCGGGTAC[A/G]TTCCGCAGATACATC | 25831 |
rs763358412 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190426 | CAGGATGAACTCACC[A/G]AGTCCAGATTGTGTC | 25831 |
rs763373035 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156030 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 25831 |
rs763377508 | snp | C/T | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099846 | ATACAATAGTTAAGT[C/T]GTGGATCTGGTGTTT | 25831 |
rs763388359 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110737 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAAATT | 25831 |
rs763389841 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157615 | TGATAATTTTAGAAA[A/C]TCAAGTAAAAAGTAC | 25831 |
rs763409000 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202570 | AAAGATTTTTACCAA[C/T]ATTCAAAATATGCAC | 25831 |
rs763424682 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143479 | AGACATTCTTAAATC[A/G]AAAAAATATATAAGG | 25831 |
rs763443646 | snp | A/C/T | 3.58258e-05 | 0.00423224 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175176 | ACGAAAGAATGCAAG[A/C/T]CTGATTTTCAAGAAT | 25831 |
rs763446139 | snp | C/G/T | 0.000100044 | 0.00707199 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150251 | TTATTCAATTAAACA[C/G/T]GGAAAATAATTTCAA | 25831 |
rs763455902 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178647 | TCTGTACTAAAAATG[A/C]AAAAAATCAGCCGGG | 25831 |
rs763474721 | snp | C/T | 1.65655e-05 | 0.00287793 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173218 | ATACAATCTATAAGC[C/T]GCCGATGTGAGCGCT | 25831 |
rs763482907 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182338 | GGGACCACAGGTGTA[C/T]GCCAACACGCCGAGC | 25831 |
rs763495074 | in-del | -/AG | 1.67105e-05 | 0.0028905 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205748 | CAAATGGTTGAAAAC[-/AG]ATGTCACTACAGTAA | 25831 |
rs763497573 | snp | C/T | 8.28013e-05 | 0.0064338 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150110 | ATAATTCCAAGGCTG[C/T]TGCATCACTCCAAAT | 25831 |
rs763502657 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200964 | TTAGACTATTAGGCA[C/T]ATAAGGTGCTGTATT | 25831 |
rs763508731 | snp | C/T | 4.83851e-05 | 0.00491836 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141889 | TTTCACTAAAGGCAG[C/T]TTTAAAAACATTTAT | 25831 |
rs763563502 | snp | C/T | 1.6764e-05 | 0.00289512 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100902 | AGTATTTTTAAAGTC[C/T]CTGATGTCTCCCATT | 25831 |
rs763571015 | snp | C/T | 1.97842e-05 | 0.00314511 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133675 | CCAAGTTGCAGTTGA[C/T]CTGTTAATATGTTAG | 25831 |
rs763571396 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110545 | TGGCATTAAATGGTA[-/C]AAAAATGTAACTATC | 25831 |
rs763591018 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159470 | TCAGTCTCCAGAGTA[-/G]TTGTGATTACAGGTG | 25831 |
rs763594486 | in-del | -/ATA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108982 | ACACAGACCAGTGAT[-/ATA]ATACCAAGCACAATT | 25831 |
rs763673279 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101079 | CAACCTACAACAAGA[A/G]AGCAAACACAACAGA | 25831 |
rs763680513 | snp | C/T | 1.65732e-05 | 0.00287859 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175049 | TTTATGAACTAGATG[C/T]CCACTGTCACGAATG | 25831 |
rs763714471 | snp | C/T | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119844 | CTCCGGCGTCCTCCT[C/T]TAGTTTCGTACTCTT | 25831 |
rs763717432 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204287 | ATTGCTGGGTCAAAC[A/G]GTATTTCTAGTTCTA | 25831 |
rs763724166 | snp | C/T | 1.65844e-05 | 0.00287957 | missense | HECTD1 | GRCh38.p7 | 14:31113287 | CAGACCTTCCTGGGA[C/T]ATTCTTGAATAAGGG | 25831 |
rs763737763 | snp | A/G | 1.65949e-05 | 0.00288048 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121392 | TATTACCTGCTCCCC[A/G]ATAGGTCGGCTCCCT | 25831 |
rs763749195 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122624 | GGACTACAAATGTCA[A/C]AGTGTGGGACTACAG | 25831 |
rs763760019 | snp | C/T | 0.000271771 | 0.0116538 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144205 | AAAAGTACAATTAGG[C/T]TTTCTAAAGCTGTCT | 25831 |
rs763765447 | snp | C/T | 1.65614e-05 | 0.00287757 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129135 | AACTATACTGTGTTC[C/T]ATTACAATTTCTGAT | 25831 |
rs763766174 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127065 | CAACCCCCACCTCCC[A/G]GGTTCAAGCGATTCT | 25831 |
rs763773425 | snp | A/G | 1.80426e-05 | 0.00300349 | missense | HECTD1 | GRCh38.p7 | 14:31113144 | GTAATTTTTTTGCTA[A/G]TGAATTCATCTGGTG | 25831 |
rs763788021 | snp | A/G | 4.0715e-05 | 0.00451174 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156796 | TTTTCCTCAAAAAAA[A/G]AAAAAAAACTCTTCC | 25831 |
rs763816486 | snp | C/G | 0.000182474 | 0.00955007 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156900 | ACCTGCCAACGTTGA[C/G]ACTTTGCTAATTACA | 25831 |
rs763829966 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137498 | TTCAGGAGTCTGAGG[C/G]AAGAGGATCAATTGC | 25831 |
rs763873374 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112172 | GCCAAAGGAACAACT[C/T]CATGTTTTCTAAAAG | 25831 |
rs763889583 | snp | A/G | 1.65669e-05 | 0.00287805 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31100993 | TCTCATGATCTCCTC[A/G]GAAGAATATTCAGGC | 25831 |
rs763894814 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144306 | AAAACATAAACATAG[C/T]TCTTAAAATAACTTA | 25831 |
rs763904740 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199921 | AACCTCCACAGGTGC[G/T]TGACTCTAAAATTTT | 25831 |
rs763915177 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196298 | TCGGGATTACAAGCA[C/T]GAGCCACCGTGTTCA | 25831 |
rs763925222 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170997 | TTGGCAGATTACAGA[A/C]ACCTAGTTCATACAT | 25831 |
rs763946273 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187028 | AGAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 25831 |
rs763946788 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202906 | CCATCCTGGTCAACA[C/T]GGTGAAACCCCATCT | 25831 |
rs763955121 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31123948 | TTTCTCAGGTTGAAA[C/G]GTCTACATTTTTAAA | 25831 |
rs763956971 | in-del | -/T | 1.65611e-05 | 0.00287755 | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134997 | ACGAGCATGACGAAG[-/T]GTATATGCTGATGGT | 25831 |
rs763970973 | snp | A/G | 3.31246e-05 | 0.00406955 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136580 | GTAGCCAAAGGTTCC[A/G]TCTTCAACATTCTGC | 25831 |
rs763987136 | snp | C/T | 0.000182771 | 0.00955784 | missense | HECTD1 | GRCh38.p7 | 14:31107037 | TCATATTGCTTTTAA[C/T]GTCACCCATACACAT | 25831 |
rs764008832 | snp | A/G | 0.000215287 | 0.0103729 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173249 | CCCCAGAACTATCTA[A/G]TCTCCGGAGTCCTGG | 25831 |
rs764009811 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31150515 | ACAGGTCCAAGCCAC[A/G]GCACCTGGCTCTCAA | 25831 |
rs764019911 | snp | A/G/T | 3.31863e-05 | 0.00407336 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148856 | CAATTTAACATATTC[A/G/T]TTTATTTGTACCCAA | 25831 |
rs764022151 | snp | C/G | 1.6577e-05 | 0.00287893 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135584 | ACAAAAACAAATGAA[C/G]ATCGGTCAAAATCAT | 25831 |
rs764095323 | snp | G/T | 1.65899e-05 | 0.00288005 | missense | HECTD1 | GRCh38.p7 | 14:31103039 | AAGGAACTTAATTTC[G/T]CCATTGGAAAAACTT | 25831 |
rs764100709 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184685 | GTTCAAGGCTGCAGT[A/G]AGCCATGATCACGCA | 25831 |
rs764111289 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31121523 | AAAATAAAACAATCC[C/G]AAGAGATACATGTCT | 25831 |
rs764122760 | in-del | AACAGATACA/CAAACAGATACATGTG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156550 | ACACACACACACACA[AACAGATACA/CAAACAGATACATGTG]TGTGTCTGAAAAAAT | 25831 |
rs764146288 | snp | A/C | 1.68312e-05 | 0.00290092 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31114059 | CTATAGACCAGCAAC[A/C]CTACAACAGGAAAAA | 25831 |
rs764149275 | snp | A/G | 4.96931e-05 | 0.00498439 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168251 | GATAAATAAAACCAT[A/G]TAATTGGTGTAATTT | 25831 |
rs764165316 | snp | A/G | 1.71755e-05 | 0.00293044 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129432 | GCCACCAGCATCCCA[A/G]GTGACATCAATCCAG | 25831 |
rs764174252 | snp | A/C | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205895 | ATCTCCCTGTCCCAT[A/C]TGTAGCCATTCCAGC | 25831 |
rs764188042 | snp | C/T | 1.6713e-05 | 0.00289072 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173665 | ATGCTGATGATGGTC[C/T]TGAAACAGTACCACC | 25831 |
rs764192063 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166578 | TTCTCAAGCCAAGTG[C/T]GGTAGCTCATGCCTG | 25831 |
rs764222422 | snp | C/T | 2.04807e-05 | 0.00319999 | missense | HECTD1 | GRCh38.p7 | 14:31109594 | TCTGTAACCATACTA[C/T]TGCTCTGAAATAGAA | 25831 |
rs764321329 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174257 | ATAAGATTATAAATA[C/T]TGTCTTATGCCTGGC | 25831 |
rs764347789 | snp | A/G | 3.33695e-05 | 0.00408456 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173543 | TGTTACTACCGGAGA[A/G]CCTCTGCAAAGTGTT | 25831 |
rs764349966 | snp | C/G | 1.66001e-05 | 0.00288094 | missense | HECTD1 | GRCh38.p7 | 14:31116422 | CGAGGTGACGGAGTA[C/G]ATTCGACTTCTTCCA | 25831 |
rs764350506 | in-del | -/TAAAAGAACAAAAATATAGTT | 1.67449e-05 | 0.00289347 | splice-acceptor-variant | HECTD1 | GRCh38.p7 | 14:31101326 | TCAGGAAACCAGGGC[-/TAAAAGAACAAAAATATAGTT]ATATTGAGTTGACTG | 25831 |
rs764361927 | in-del | -/GTGTGA/GTGTGTGA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122285 | TGTGTGTGTGTGTGT[-/GTGTGA/GTGTGTGA]GAGATTCTGTGGCTC | 25831 |
rs764367460 | in-del | -/ATC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125495 | TCTTTCCTACCCACA[-/ATC]ATCTTCAACTTCCCA | 25831 |
rs764383101 | in-del | -/AAC | 2.06411e-05 | 0.0032125 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135226 | GAAAAATTAGCAAAT[-/AAC]AACGTTAAGATAATT | 25831 |
rs764399074 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155680 | TCAGGACAAACTATC[A/G]CAGGTTCTCAGGAAT | 25831 |
rs764401277 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139420 | GAACACAGTTAGAAG[G/T]TTCCATCTAAGAGGA | 25831 |
rs764411465 | snp | A/C | 1.72791e-05 | 0.00293926 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101369 | GTTGACTGCAGATTT[A/C]AATGAAAATCACTAC | 25831 |
rs764427041 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199577 | AAAATTAGCTGGACA[C/T]GGTGGCGCACACCTG | 25831 |
rs764479168 | snp | C/T | 9.95553e-05 | 0.00705463 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139982 | TAACTTTCGAATTAA[C/T]GCAACTGCTGGTCGA | 25831 |
rs764487359 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154600 | ACTGCACTCAGCCTA[G/T]AATCTCCTTGTCAAT | 25831 |
rs764487738 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31106574 | ATATATTGCAAATCA[A/G]TGACGACAAAGAAAC | 25831 |
rs764520750 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193302 | ATGGATATCCAATTG[-/T]TTTCAGCATCACAAA | 25831 |
rs764525636 | snp | A/C | 1.74964e-05 | 0.00295769 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128567 | CTATTTTGCATCCCT[A/C]CAAGTGGAAAAAGCA | 25831 |
rs764532209 | snp | A/T | 1.65943e-05 | 0.00288043 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136707 | GGAAAACGTCTTGGT[A/T]TCTGTCTCAGAATTG | 25831 |
rs764534213 | snp | A/T | 2.5665e-05 | 0.00358216 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149194 | TGTTTCAAAATCTTA[A/T]TTCTTTCAAGTATGA | 25831 |
rs764542645 | in-del | -/AAT | 1.67444e-05 | 0.00289343 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112557 | TCCTGCGAATTAACA[-/AAT]AATAATGTCTTAGTG | 25831 |
rs764552977 | snp | A/G | 8.28274e-05 | 0.00643481 | missense | HECTD1 | GRCh38.p7 | 14:31116318 | GCAATTTTTGTACAT[A/G]GTAAAAGATGGTTGA | 25831 |
rs764575979 | snp | G/T | 1.65732e-05 | 0.00287859 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134914 | ACATGGGTATACAAA[G/T]AAGTCCAGTTCTGTC | 25831 |
rs764619159 | snp | C/T | 1.6574e-05 | 0.00287867 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135144 | TCTTCCTTCTGATGA[C/T]GTTACTACTACAAGT | 25831 |
rs764626550 | snp | C/T | 1.68012e-05 | 0.00289833 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171993 | TCATAAAGCTGCTTT[C/T]TATTAATATTTCTAT | 25831 |
rs764630709 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180377 | ATGGCAAGACTCACT[A/G]TTAAAAAAATACATA | 25831 |
rs764640070 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153895 | ATTTTGCATATGCTA[C/T]TGGCTTGTTCATTTT | 25831 |
rs764641899 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118252 | CCTTGTGATCCACTC[A/G]CCTCAGCCTCCCAAA | 25831 |
rs764644912 | in-del | -/GTGTGTGTGTGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134558 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGC]GCGCGTATGTATATA | 25831 |
rs764660870 | snp | C/T | 1.65699e-05 | 0.00287831 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149031 | TCTCCTTCTTTCAAA[C/T]ATGTCAGTGACCAAT | 25831 |
rs764666703 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182123 | GATCTAGAACTTCTG[A/G]CCTCAAATGATCTAC | 25831 |
rs764667622 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198539 | GAGTGGTAGTCATAT[C/T]GACAAATAAGACTTT | 25831 |
rs764668065 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31119984 | TCTTAAACCCAAAAT[A/G]AGCTAACCTAAACAT | 25831 |
rs764682429 | in-del | -/CACACGCG/CACGCG | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163089 | ACACGCACACACACA[-/CACACGCG/CACGCG]CACACGCACACATGC | 25831 |
rs764696489 | in-del | -/TTT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104999 | GACCACCATCAATTC[-/TTT]TTTTTTTTTTTTTTT | 25831 |
rs764719214 | snp | A/C | 3.36236e-05 | 0.00410008 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172005 | TTTTTATTAATATTT[A/C]TATCCTTAATTTAAA | 25831 |
rs764741965 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194879 | TTGAACTTGGGCCAA[A/G]ATTTCAGAAGATTGG | 25831 |
rs764755247 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122139 | GGGTAAGTTCATACA[C/G]TGTGTGTGTGCTTGG | 25831 |
rs764772323 | snp | C/T | 1.68803e-05 | 0.00290515 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171888 | AGGTCTTCCAAAACA[C/T]GCAGCATAATGTAAT | 25831 |
rs764851230 | snp | A/G | 1.66134e-05 | 0.00288208 | missense | HECTD1 | GRCh38.p7 | 14:31106812 | ATCTGGCTCTGTGTG[A/G]GTTTACTAATTCAAA | 25831 |
rs764890856 | snp | C/T | 3.31241e-05 | 0.00406952 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134956 | ACCTGGAAAACCCAA[C/T]TTCTCAGTGCAGACC | 25831 |
rs764897709 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180660 | ATGTTGGCCAGGCTG[C/G]TATTGAACTCCTGGC | 25831 |
rs764903234 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153521 | GCCGACCATTTCAAC[A/G]TATTTTGAAGAGCGT | 25831 |
rs764912696 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112284 | CAGGCCAAAAGGCAA[A/T]GCTGACTATTCTTTA | 25831 |
rs764913747 | snp | C/T | 3.42659e-05 | 0.00413906 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177969 | ATGAGCCAATACTCA[C/T]CCCTGAGAGGTCTGA | 25831 |
rs764935981 | snp | G/T | 3.31279e-05 | 0.00406975 | missense | HECTD1 | GRCh38.p7 | 14:31113409 | GTTCTTTTGTTAAAT[G/T]AAGAATATCACTACT | 25831 |
rs764941617 | snp | A/T | 1.68148e-05 | 0.0028995 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101333 | ACCAGGGCTAAAAGA[A/T]CAAAAATATAGTTAT | 25831 |
rs764967468 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162125 | TAATCCCAGCTCCTC[A/G]GGAGGCTGAGGCACG | 25831 |
rs764971244 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145566 | GTCCCAGCTACTCAG[A/G]AGACTGAGGCGGGAC | 25831 |
rs764974551 | snp | C/T | 1.67343e-05 | 0.00289255 | splice-donor-variant | HECTD1 | GRCh38.p7 | 14:31173524 | TCAAAAACATTCTTA[C/T]ATGTGTTACTACCGG | 25831 |
rs764975645 | snp | C/G | 1.65773e-05 | 0.00287895 | missense | HECTD1 | GRCh38.p7 | 14:31106686 | GCCCAGAACCTGATG[C/G]ATTCTTCAGCACTAG | 25831 |
rs764985924 | snp | C/T | 1.66732e-05 | 0.00288727 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144837 | AAGTTCCCAAGATGA[C/T]TCTAACTGAGTTGCT | 25831 |
rs765020639 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146600 | CATATCAGGCTGGGC[A/G]CAGTGGCTTTTGGGA | 25831 |
rs765050401 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146968 | AGAAATCTAACCCAG[-/T]TATTTCTCCCACAAG | 25831 |
rs765061270 | in-del | -/T | 1.69407e-05 | 0.00291034 | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135509 | CAGTAAATGATTCCA[-/T]TTTCATCAAAATCAT | 25831 |
rs765079026 | in-del | -/AAAG | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208964 | ACTACTTCTTTAGAA[-/AAAG]AACCAGTATTTTGGA | 25831 |
rs765095530 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204410 | ACATCCTCTCCAGCA[C/T]CTGTTGTTTCCTGAC | 25831 |
rs765097051 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129255 | GCCTGCAGCAGCAGA[C/T]GTCTTGTCTGGACAG | 25831 |
rs765106677 | snp | C/T | 1.90308e-05 | 0.00308464 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144245 | CTCTCCAAGTGTTCT[C/T]ACTCTCAATACACTA | 25831 |
rs765121777 | in-del | -/TTAAAA | 4.93279e-05 | 0.00496604 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144309 | ACATAAACATAGCTC[-/TTAAAA]TAACTTATCAGAACA | 25831 |
rs765142792 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205581 | TTCATTCAACAAATA[C/T]GTATTTGTGTCATCG | 25831 |
rs765161560 | snp | C/G | 1.65831e-05 | 0.00287945 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156959 | TATCACCACCTTTAT[C/G]TACTAAATCCCTTAT | 25831 |
rs765167493 | snp | C/G | 4.97583e-05 | 0.00498765 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119888 | AAATAAAATTTCACA[C/G]ACAAACATAATAAGA | 25831 |
rs765206395 | snp | C/G | 1.65688e-05 | 0.00287821 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101170 | TCCCCATTAGCCAGA[C/G]AGCTTGTACCTTGCG | 25831 |
rs765223770 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31123989 | GCTTTGAAATCGGAA[C/T]GTATCTTACAAACAA | 25831 |
rs765228614 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201061 | GTTCCTGTACAGGTA[-/T]TTTTTTTACCTTTTA | 25831 |
rs765233467 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31109885 | AATCTGTTGTCCAAG[-/C]CCCCAACATCATTCA | 25831 |
rs765255463 | snp | A/T | 1.66007e-05 | 0.00288098 | missense | HECTD1 | GRCh38.p7 | 14:31107579 | TACGTGACGAGATTC[A/T]TCATCTGGAAAATTA | 25831 |
rs765267189 | snp | C/T | 1.66034e-05 | 0.00288122 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31113911 | TGAGAACAATTTCTG[C/T]TTTTCCTAATACTTT | 25831 |
rs765319903 | in-del | -/AA | 3.33483e-05 | 0.00408327 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121524 | AAATAAAACAATCCC[-/AA]GAGATACATGTCTAA | 25831 |
rs765330460 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207899 | GGTACGCCGCGTCGC[C/T]GTCCCTGCCCCGGAG | 25831 |
rs765344680 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175541 | TTGCATTCCCATCCT[A/G]GGCAAGAGAGTGAGA | 25831 |
rs765344697 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191369 | TGTCTCTACAATAAA[C/T]ACAAAAATAAGCCGG | 25831 |
rs765376611 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116001 | TCTTAGACAAAGAAT[G/T]CAAATGACGCTCTTT | 25831 |
rs765400636 | snp | A/G | 1.66846e-05 | 0.00288826 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205755 | TTGAAAACAGATGTC[A/G]CTACAGTAACCCAAA | 25831 |
rs765401928 | snp | G/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164134 | CTACTCCACCACTGA[G/T]ACTACCAATCTCTGT | 25831 |
rs765429669 | snp | C/T | 7.93242e-05 | 0.00629728 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173779 | GGTCAGCCAGTGATG[C/T]AAAGCATCGCAGAGC | 25831 |
rs765435257 | snp | A/G | 0.000186202 | 0.0096471 | intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31123556 | TAATCTCTTGCCTTC[A/G]ATGGAGACTGGGTCA | 25831 |
rs765481555 | snp | C/T | 1.65836e-05 | 0.0028795 | missense | HECTD1 | GRCh38.p7 | 14:31112462 | AAAGCTGTCTAGTTT[C/T]AAATGGTATTAGAAA | 25831 |
rs765482429 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157390 | ACAGTAAAATATCCA[A/C]TGTTACATTTTATAC | 25831 |
rs765499753 | snp | C/G | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122973 | TCTCATCATCTTCTT[C/G]ATCTGGCTCAGGTAA | 25831 |
rs765512991 | snp | C/T | 1.65641e-05 | 0.00287781 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168265 | TATAATTGGTGTAAT[C/T]TGACTAACACATCAA | 25831 |
rs765531166 | in-del | -/CATG | 1.65479e-05 | 0.0028764 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112587 | GTGCTATAAGGCATT[-/CATG]CATGCATGCATTCAT | 25831 |
rs765535673 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141744 | ATAATATGTTACTTT[A/C]TTATTAAGAGTTTCT | 25831 |
rs765537326 | snp | C/T | 1.67449e-05 | 0.00289347 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103070 | TATTAAACCCATCTA[C/T]ATCGTACATGTAACG | 25831 |
rs765562723 | in-del | -/ACAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171115 | TCTAGTGATTCTTCT[-/ACAA]ACAGAGTATTTGGCT | 25831 |
rs765566192 | snp | C/T | 0.000638473 | 0.0178558 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173686 | CAGTACCACCAGCAG[C/T]AGCCATTCGAGATAA | 25831 |
rs765612933 | in-del | -/GAGGCT | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31162991 | ACTGCTTGAGCCCAG[-/GAGGCT]GAGGCTGAGGCTGCA | 25831 |
rs765613331 | snp | A/G | 5.82157e-05 | 0.00539485 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141866 | ATTTTACCTTTCATC[A/G]TCTTCATTTTCACTA | 25831 |
rs765619011 | snp | C/T | 1.66175e-05 | 0.00288244 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133283 | CTCCCTGTGGGCTGC[C/T]ATCCTGATCTCGCCA | 25831 |
rs765621221 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127736 | GAAAACATAATAAAA[A/G]CATCATTATGAAAGT | 25831 |
rs765662846 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154777 | GTAACACATACACAC[A/T]CTCTCTTTCACCACC | 25831 |
rs765672427 | snp | C/T | 5.29404e-05 | 0.00514465 | intron-variant | HECTD1 | GRCh38.p7 | 14:31129460 | CAGCCTGGAAAGGGA[C/T]AGGAGTTTGTGAGAC | 25831 |
rs765718315 | snp | C/T | 4.97113e-05 | 0.00498529 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128835 | TGACAGTCTGTTACT[C/T]GCTGAAGAGCTAAGA | 25831 |
rs765731977 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150096 | ATTACTGCCATTAGA[C/T]AATTCCAAGGCTGCT | 25831 |
rs765754063 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189710 | CCAGGAGGTAGAGGC[C/T]GCAGTGAGCTGCATT | 25831 |
rs765798209 | snp | A/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209226 | AATGTAGACACTGAA[A/G]GGAAAGGGAAGAACA | 25831 |
rs765839894 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200848 | CACCTCTCCAGGTCT[C/T]GTCCCTGCTTCATGC | 25831 |
rs765861228 | snp | C/T | 3.31208e-05 | 0.00406931 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150152 | CCCTTCCCCTAATGA[C/T]TGACCAGTCTCTCCA | 25831 |
rs765863793 | in-del | -/GTGTGTGTGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134560 | TGTGTGTGTGTGTGT[-/GTGTGTGTGC]GCGCGTATGTATATA | 25831 |
rs765868284 | in-del | -/AA | 1.67912e-05 | 0.00289747 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100896 | TTCACTAGTATTTTT[-/AA]AGTCTCTGATGTCTC | 25831 |
rs765871436 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201044 | TTTAAAGTTAAAAAA[C/T]TTGTTCCTGTACAGG | 25831 |
rs765905418 | snp | C/T | 0.000105882 | 0.00727528 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173106 | ACTAGAAACTGCCTA[C/T]ATGGTTATCTCACAA | 25831 |
rs765946669 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31173816 | TGAAACCTAACAATG[C/T]GAAGAAAATGCCCAC | 25831 |
rs765959865 | snp | C/T | 3.3184e-05 | 0.00407319 | missense, nc-transcript-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121399 | TGCTCCCCAATAGGT[C/T]GGCTCCCTGCTCCAG | 25831 |
rs765973033 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184096 | CATAATTCTAAAAAC[G/T]TTTCTTTAAAACAAC | 25831 |
rs765992740 | in-del | -/AAG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31121698 | ACTAACCTCCTTCAT[-/AAG]AAGTATTGTGTTTTC | 25831 |
rs766020309 | snp | C/G | 1.65633e-05 | 0.00287774 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128977 | ACAGAACTATCAGGG[C/G]CTAACTTCCTTTCAG | 25831 |
rs766037823 | snp | A/T | 1.66114e-05 | 0.00288192 | missense | HECTD1 | GRCh38.p7 | 14:31107010 | CACCTCGTGACTCAT[A/T]AATCAGTTTACTCAT | 25831 |
rs766040230 | snp | A/T | 1.67925e-05 | 0.00289758 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172008 | TTATTAATATTTCTA[A/T]CCTTAATTTAAATAC | 25831 |
rs766047555 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146827 | CACTGCCCTCCAACA[C/T]AGGAAACAGAGTGAG | 25831 |
rs766058450 | snp | A/G | 1.72946e-05 | 0.00294058 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113857 | TGCAATCAAAATAGT[A/G]TTTTGATGCCAATAT | 25831 |
rs766063051 | in-del | -/AATT | 3.74974e-05 | 0.00432982 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144977 | AATGTGAATTTTTAC[-/AATT]AATAATTTTACCAAA | 25831 |
rs766067601 | snp | C/T | 1.72481e-05 | 0.00293662 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144939 | TCGAGCCATAGTTCG[C/T]ACCTACCAAAATAAA | 25831 |
rs766075434 | snp | C/T | 1.65679e-05 | 0.00287814 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128859 | GCTAAGAGGTCGTTG[C/T]GAAGCTGCTTCTTTA | 25831 |
rs766084278 | snp | A/G | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178155 | AGATACATCCAGGTA[A/G]TATGTTATGGCACGG | 25831 |
rs766099836 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147470 | AAATGAAAACCACTA[C/T]CACAGGACTGGCACA | 25831 |
rs766106911 | snp | A/T | 3.52566e-05 | 0.00419846 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178275 | GTGAAAGAAATCATA[A/T]TACATCTAGGGTTAT | 25831 |
rs766177634 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31169781 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATCGC | 25831 |
rs766181595 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102809 | AGACACCACTGCTTT[C/G]TCACTTACTTTATGA | 25831 |
rs766183572 | snp | A/G | 1.65707e-05 | 0.00287838 | missense | HECTD1 | GRCh38.p7 | 14:31113430 | TATCACTACTTTGAA[A/G]AGTAGAAATGGCCCC | 25831 |
rs766186544 | snp | C/T | 3.53163e-05 | 0.00420201 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157335 | AGAATTATATGAAGC[C/T]AAATGAAGTTAAAAT | 25831 |
rs766195016 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120105 | GATAACCATTCATGG[C/T]CAGACATGGTGGCTG | 25831 |
rs766197073 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134399 | CAGCCTTAATTCTAT[A/C]ACGAGCAATAGCCAC | 25831 |
rs766203387 | snp | G/T | 3.32962e-05 | 0.00408007 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135169 | ACAAGTCCATAGGCA[G/T]CTGGATTTACCCATT | 25831 |
rs766211600 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138071 | TACAAATCTGGAATC[C/T]TGAAATGCTCCAAAA | 25831 |
rs766228985 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193244 | ATCTGGGTTTTTAAA[A/T]ATATATATAGTGTGA | 25831 |
rs766236694 | snp | C/G | 1.65899e-05 | 0.00288005 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121493 | GACGTTGCAGGGATG[C/G]GCGTCTCAGAATCTA | 25831 |
rs766258183 | snp | A/G | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134993 | AACCACGAGCATGAC[A/G]AAGTGTATATGCTGA | 25831 |
rs766264715 | in-del | -/ATT | 1.80762e-05 | 0.00300629 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156825 | CCTGATACCTCTATA[-/ATT]AAGACCACTCACTTT | 25831 |
rs766272323 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31162176 | GTCAGAGGTTTGCAG[C/T]GAGCCAAGATCATGC | 25831 |
rs766287040 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133030 | CTTACACTAGGCTTG[A/G]TCACTTCCAAAATAC | 25831 |
rs766296405 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31173877 | TGATCATTTCAATAC[C/T]GACACTATAAGAAAG | 25831 |
rs766332247 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160994 | ATTTTTCCATATTAA[C/T]TTTTTGCCGTGTTTC | 25831 |
rs766352815 | snp | A/G | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157187 | TCCAGGACAGTTGCA[A/G]TGATTTCCACTAGTA | 25831 |
rs766359449 | snp | G/T | 1.65872e-05 | 0.00287981 | missense, nc-transcript-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121408 | ATAGGTCGGCTCCCT[G/T]CTCCAGCAGGTACCT | 25831 |
rs766368801 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206045 | TTCCTTTACATCTGC[C/T]AGAACCAAATTTTCA | 25831 |
rs766368896 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124757 | CCTGCACATATATCC[-/T]CCTGAATCTAAAATA | 25831 |
rs766373690 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196147 | GCCTCCTGAGAAGCT[A/G]GGATTACAGGAATGT | 25831 |
rs766375650 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167239 | GGAGGCTGAGGTGGG[C/T]GATCACTTGAGCCCA | 25831 |
rs766381013 | snp | A/G | 1.66804e-05 | 0.00288789 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144855 | TAACTGAGTTGCTAT[A/G]TTTCTGAGTGTTACC | 25831 |
rs766384773 | snp | A/G | 1.65644e-05 | 0.00287783 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205909 | TCTGTAGCCATTCCA[A/G]CAATGTATCTGGGTC | 25831 |
rs766388695 | snp | C/G | 1.88007e-05 | 0.00306594 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107265 | CAACCTAATTTTTTA[C/G]AGGGTGAAATGCAAA | 25831 |
rs766404671 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135871 | AAAAATACAAAAATT[A/G]GCCAGGCGTGGTGGC | 25831 |
rs766420959 | snp | C/T | 3.31235e-05 | 0.00406948 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136631 | GTTTCACCAGGTGCA[C/T]GTTCCAACCGAAATC | 25831 |
rs766438903 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152550 | CATCATCACATTTAC[A/T]ATATCCAGTAGCAAA | 25831 |
rs766447879 | snp | A/G | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127904 | GTTGTTGCTGTAGCT[A/G]CATTGCTGCTGCTAG | 25831 |
rs766467398 | in-del | -/TCT | 1.65623e-05 | 0.00287765 | cds-indel, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122966 | TCTTCATTCTCATCA[-/TCT]TCTTCATCTGGCTCA | 25831 |
rs766471714 | snp | A/C | 1.65927e-05 | 0.00288029 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148870 | CATTTATTTGTACCC[A/C]ATAAACTTACATATC | 25831 |
rs766501040 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198371 | TTTTTCAAAATTTAA[A/T]CACGTATGCCTTTCA | 25831 |
rs766501793 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165342 | CTGCCAAACTCTTAA[A/G]TTTGTTCTCACTAAT | 25831 |
rs766522027 | snp | A/G | 1.66076e-05 | 0.00288158 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169339 | TGGCTTCAAAAGAAA[A/G]AATGTAGCTCTCACC | 25831 |
rs766548828 | in-del | -/A | 1.67172e-05 | 0.00289108 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133485 | GTTTTAGTAAGTTAG[-/A]AAAGCCTCGTATCAT | 25831 |
rs766549516 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104849 | AGCTAATTTTTTAAA[A/G]AATGTTTTGTAGAGA | 25831 |
rs766556705 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151162 | ATAATCTCTATATAG[A/T]TAATAGAGACAGGGT | 25831 |
rs766576619 | snp | G/T | | | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31112538 | ACTTGCCAGTGCCAA[G/T]GGTTCCTGCGAATTA | 25831 |
rs766586355 | snp | A/T | 7.23912e-05 | 0.00601584 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114367 | GATATTCAAGTTAAT[A/T]CATATATAATTTGTG | 25831 |
rs766600514 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31106100 | GTGTACAAAAATATA[C/T]ATTAAAAAAAACCTT | 25831 |
rs766636922 | snp | A/G | 1.65682e-05 | 0.00287817 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148787 | AGTCCAGCCAGTCAC[A/G]AATTCTGAACCTTGG | 25831 |
rs766637588 | snp | A/G | 1.75631e-05 | 0.00296332 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114095 | TGTTGGCCTTTCCCA[A/G]TTATAAAGTCTATGA | 25831 |
rs766669557 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165970 | CCTGACTCACCCTCC[C/G]GAGTAGCTGGGACTA | 25831 |
rs766686852 | snp | A/G | 1.6838e-05 | 0.0029015 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105703 | TAAATTAACTGACAT[A/G]CAGCTACTACTAATG | 25831 |
rs766737327 | snp | A/C | 1.67077e-05 | 0.00289026 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133433 | TCAGGTAGAAATTGG[A/C]GAAATAAAAACCAAA | 25831 |
rs766742972 | snp | A/G | 4.9755e-05 | 0.00498748 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133305 | ATCTCGCCATTTCCA[A/G]TCCAGGCCTCTGATA | 25831 |
rs766759742 | snp | C/T | 1.6563e-05 | 0.00287771 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168402 | TTTGGGCTCATTACA[C/T]TCTTCTTCATCTTTG | 25831 |
rs766770196 | snp | C/G | 0.000186133 | 0.0096453 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123645 | AAAAAGAGGACTAAA[C/G]GGATTATAACAGAAG | 25831 |
rs766770574 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188481 | CCTTGTGATACACCC[A/G]CCACGGCCTCCCAAG | 25831 |
rs766784775 | snp | C/G | 1.65669e-05 | 0.00287805 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175022 | CACAGCCATAGCAGA[C/G]TGCAAGGTGTCTTTA | 25831 |
rs766787745 | snp | C/T | 1.65905e-05 | 0.0028801 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31112484 | TATTAGAAAAGGACA[C/T]TTGCTGGTTAATTGT | 25831 |
rs766797998 | snp | G/T | 2.40255e-05 | 0.00346586 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141891 | TCACTAAAGGCAGTT[G/T]TAAAAACATTTATTC | 25831 |
rs766841763 | snp | A/C | 1.66579e-05 | 0.00288595 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119678 | ATTTAGTATGTATTA[A/C]AATTAAATCACAAAA | 25831 |
rs766845658 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110787 | AAAAGCTGGAATTAC[A/G]CCCAGCTAATTTTTG | 25831 |
rs766862004 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141988 | AAAGTCCAAAAAAAA[A/G]TAATTTAAGGATCTT | 25831 |
rs766868010 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130948 | ACATAGCCCAATCTC[-/A]AATAAAAGTAACTTT | 25831 |
rs766873714 | snp | A/C | 2.27368e-05 | 0.00337163 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173811 | CCATCTGAAACCTAA[A/C]AATGTGAAGAAAATG | 25831 |
rs766916216 | snp | A/G | 6.01576e-05 | 0.00548409 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109634 | TGAGCTGCAGCATAC[A/G]TTAACAGCTGAATGT | 25831 |
rs766954380 | snp | A/G | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099985 | TCAATTTTAATACCC[A/G]TATTTACTATAGAAA | 25831 |
rs766967812 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189837 | TCTACCTCCCACCCC[A/C]CATAATCTTTTTTAA | 25831 |
rs767024540 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143648 | TTTTGAACAGCTTTA[G/T]GATATGCTTAGGTAG | 25831 |
rs767050092 | snp | A/G | 5.56757e-05 | 0.00527586 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174866 | GGGGAACACTAAAAA[A/G]ATCACTTTCTGAAAA | 25831 |
rs767076229 | snp | C/T | 3.32e-05 | 0.00407417 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31112496 | ACATTTGCTGGTTAA[C/T]TGTTCACACCAGTCT | 25831 |
rs767102441 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110921 | TAGGCATGGGCCACC[A/G]TGCCCAGCCTGAAAA | 25831 |
rs767124098 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170888 | AAATTGTCCAAGATC[A/T]TATAGCCTTTTTTGT | 25831 |
rs767150352 | snp | A/T | 5.00613e-05 | 0.00500281 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173121 | TATGGTTATCTCACA[A/T]CTTTCTTTTTATATT | 25831 |
rs767153410 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147132 | TCCTGGCTAACACAG[G/T]GAAACCCTGTCTCTA | 25831 |
rs767155894 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111910 | CGCTTGAACCTGGGA[A/G]GCGGAGGTTGCAGTG | 25831 |
rs767160057 | snp | A/T | 3.34605e-05 | 0.00409012 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150262 | AACATGGAAAATAAT[A/T]TCAATTTCAAATATT | 25831 |
rs767167801 | snp | A/G | 4.96899e-05 | 0.00498422 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119836 | CCCATGTTCTCCGGC[A/G]TCCTCCTTTAGTTTC | 25831 |
rs767178520 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203794 | AGGGTACATGTGCTC[-/A]ACGTGCAGGTTTGTT | 25831 |
rs767187305 | snp | C/T | 0.000133225 | 0.00816055 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135538 | ATGCTGGTGCCGAAA[C/T]ATAAAATTTTGTCCT | 25831 |
rs767188827 | snp | A/T | 6.6268e-05 | 0.00575583 | missense | HECTD1 | GRCh38.p7 | 14:31100983 | GCAGGCGCTCTCTCA[A/T]GATCTCCTCGGAAGA | 25831 |
rs767199735 | in-del | -/TGTGTG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134527 | GCATAAATGTGTGTG[-/TGTGTG]TGTGTGTGTGTGTGT | 25831 |
rs767212702 | snp | A/C | 1.66109e-05 | 0.00288187 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119693 | AAATTAAATCACAAA[A/C]CCAAAACATTCTGTA | 25831 |
rs767220887 | in-del | -/AAG | 3.31373e-05 | 0.00407032 | cds-indel, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31174964 | CTACACAAATTTCTA[-/AAG]AAGAATCTTGAGGCT | 25831 |
rs767220928 | snp | A/G | 1.65608e-05 | 0.00287752 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129090 | AGCAGATGAAAGAAC[A/G]ACAATTGGTTCATGG | 25831 |
rs767248159 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157669 | GGGCCCAGTGCAGCG[A/G]CTCACGCGTGTAATC | 25831 |
rs767256378 | snp | C/T | 6.62504e-05 | 0.00575507 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173232 | CTGCCGATGTGAGCG[C/T]TCCCCAGAACTATCT | 25831 |
rs767277795 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103859 | ATAATCCCAGCTACT[C/T]GGGAGGCTGAAGCAG | 25831 |
rs767308820 | in-del | -/TTC | 3.31246e-05 | 0.00406955 | cds-indel, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168402 | TTTGGGCTCATTACA[-/TTC]TTCTTCATCTTTGTT | 25831 |
rs767311873 | snp | G/T | 1.6741e-05 | 0.00289314 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148718 | CACATCCAACAGATA[G/T]ACCTTTTGCTTTGTT | 25831 |
rs767322747 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194048 | CCATGAAAAGGAATA[C/T]TACTTAGCAACTAAA | 25831 |
rs767325037 | snp | A/G | 1.66128e-05 | 0.00288204 | missense | HECTD1 | GRCh38.p7 | 14:31107012 | CCTCGTGACTCATAA[A/G]TCAGTTTACTCATAT | 25831 |
rs767337424 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128991 | GCCTAACTTCCTTTC[A/G]GCATTTTCACTTCCC | 25831 |
rs767348011 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122531 | CTCAGGCTGGAGTGC[A/G]GTGATGCAATTATAG | 25831 |
rs767352855 | in-del | -/TAAT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170507 | ATTTCATACCCAGAC[-/TAAT]TAATCACAATGGCTC | 25831 |
rs767362642 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135760 | TGCGGTGGTTCACGC[C/T]TGTAATCCCAGCACT | 25831 |
rs767365954 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184513 | GGATGGCTTGAGTCT[C/G]AGAGGCAGAGGTTGC | 25831 |
rs767371254 | in-del | -/CT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135984 | GATTGTGCCACTGCA[-/CT]CCAGCCTGGCAACAG | 25831 |
rs767377904 | snp | A/G | 6.78725e-05 | 0.00582509 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113873 | TTTTGATGCCAATAT[A/G]TACCTTATATGCAGC | 25831 |
rs767390756 | snp | C/T | 1.6566e-05 | 0.00287797 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128891 | TAGTTAATTCAGATA[C/T]TGAACTAACATCAGG | 25831 |
rs767420295 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115939 | GTGTTAACCCACACA[A/C]CCCCAAAATCAAGAA | 25831 |
rs767437720 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31121916 | GAGTTCTGGATCACA[C/T]TGCCTATGCTTGGGT | 25831 |
rs767439229 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164036 | CAGACCTGTTCAAAA[C/T]TCTATGTAGCTTTCT | 25831 |
rs767451398 | snp | G/T | 3.31241e-05 | 0.00406952 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168380 | TGGGTGCCATTTCCG[G/T]ATCTCCTTTGGGCTC | 25831 |
rs767518218 | snp | A/C | 1.65751e-05 | 0.00287876 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173409 | AATTGAATCTGGAAG[A/C]TCCGACCTCAGAAGA | 25831 |
rs767519029 | snp | A/G/T | 8.3464e-05 | 0.00645955 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173538 | ACATGTGTTACTACC[A/G/T]GAGAGCCTCTGCAAA | 25831 |
rs767550410 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122966 | TCTTCATTCTCATCA[C/T]CTTCTTCATCTGGCT | 25831 |
rs767576429 | in-del | -/TAAAAA | 7.73126e-05 | 0.00621694 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144031 | CTTGACAAAACAAAC[-/TAAAAA]CCACTCTACCGAAGG | 25831 |
rs767595128 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195132 | TTTCTTGGTATTGCT[A/G]AGCTAAAAATAACTC | 25831 |
rs767603672 | snp | C/G | 1.65726e-05 | 0.00287855 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139957 | GTTCAATAGATTCTA[C/G]TACAGCTATTAACTT | 25831 |
rs767658930 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185640 | GCTGAGATGGGAAGA[C/T]CACATGAGCCCAGGG | 25831 |
rs767682036 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110879 | CGAGTGATGTGTCTG[C/G]CTTGGCCTCCCAAAG | 25831 |
rs767715938 | snp | A/G | 1.65707e-05 | 0.00287838 | missense | HECTD1 | GRCh38.p7 | 14:31101185 | GAGCTTGTACCTTGC[A/G]TACAACCGTGAGCCT | 25831 |
rs767825365 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130723 | ATGATAGCACTCAGA[G/T]GGAAATAATATTGAA | 25831 |
rs767828012 | snp | C/T | 1.66377e-05 | 0.00288419 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114391 | ATTTGTGATTATTTC[C/T]AATAAGGCTTCAATT | 25831 |
rs767835292 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176936 | GCAAGACTATCTCTC[-/A]AAAAAAAAAAAAAAA | 25831 |
rs767847054 | snp | A/G | 1.65861e-05 | 0.00287972 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31107597 | ATCTGGAAAATTATC[A/G]TCACAAAGCCAAGCT | 25831 |
rs767882834 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177050 | CATAAAGACAACAGC[C/T]TACTTTACAGGGAAT | 25831 |
rs767896610 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117018 | ACATGTGTATGATAG[A/G]GAGCTCTCTCATTTT | 25831 |
rs767924943 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31166399 | CTAGCGTAAGTGTAA[C/T]GGGCCAAATGTTAGG | 25831 |
rs767935311 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105095 | GCAACCTCACCTCCC[A/G]GGTTCAAGCAATTCC | 25831 |
rs767938620 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196919 | CACAAATACCTTCCA[C/T]GGGCATTTTAGGCAT | 25831 |
rs767941649 | snp | A/G | 1.70165e-05 | 0.00291684 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106629 | ATTGGATTGAAGAAT[A/G]TACATATAATGCTTA | 25831 |
rs767954866 | snp | A/C | 1.66087e-05 | 0.00288168 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133609 | TTTCCCCATCTGTTT[A/C]ATTCTCACATGTCTC | 25831 |
rs767957790 | snp | C/T | 4.9689e-05 | 0.00498418 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127908 | TTGCTGTAGCTACAT[C/T]GCTGCTGCTAGTAAC | 25831 |
rs767958186 | snp | C/T | 1.65707e-05 | 0.00287838 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175043 | GGTGTCTTTATGAAC[C/T]AGATGTCCACTGTCA | 25831 |
rs767960330 | snp | A/G | 6.13892e-05 | 0.00553993 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113076 | CAACAGTAATAGAAT[A/G]AAGAGTTCAGCTGTC | 25831 |
rs768000959 | snp | A/C | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100646 | ACTGAAGATCTGAGA[A/C]GCTGCTCTTTGGAAC | 25831 |
rs768026070 | snp | A/T | 1.6867e-05 | 0.002904 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144798 | ATTAAAATCTAGAGG[A/T]TGACATACTTGTCTA | 25831 |
rs768034919 | snp | C/T | 1.65611e-05 | 0.00287755 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169412 | TCGAGCTTTATCTAA[C/T]GGAGTTTTCCCATCT | 25831 |
rs768073506 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127386 | GAAGGAGTTTCGCTC[C/T]TGTTGCCCAGGCTGG | 25831 |
rs768104663 | in-del | -/ATTTTAAGG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129676 | TCTCATGATACAAAT[-/ATTTTAAGG]ACAAGAAATATGTAC | 25831 |
rs768106922 | in-del | -/CTT | 8.28411e-05 | 0.00643535 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101113 | CCATGAGTTTAAATA[-/CTT]CTTTCTTTCAAAAGT | 25831 |
rs768122107 | snp | A/G | 1.65627e-05 | 0.00287769 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129353 | ATGCCACTGTATCAG[A/G]GTCGTACCCTGGTGC | 25831 |
rs768168750 | snp | C/G | 1.65784e-05 | 0.00287905 | missense | HECTD1 | GRCh38.p7 | 14:31109539 | TCTCGCCTAACACTG[C/G]TTGTGGTTCTCGTTC | 25831 |
rs768217190 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146365 | CCCTATTCACAATCT[-/A]CTTAGTGTCACATAT | 25831 |
rs768225904 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146313 | TTCAAAAAGGTGACA[C/T]TCTTTCTTGCTTCAG | 25831 |
rs768237448 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174646 | CCAAGTCAGCAAAAT[G/T]ACACTCAGTACAAGT | 25831 |
rs768245623 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161728 | TTCGAGACCAGCCCA[A/G]CCAACATGGCAAAAC | 25831 |
rs768250822 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124708 | ATCAATAGAAGTCCA[A/G]ATCTCAGCATCACAC | 25831 |
rs768255808 | snp | A/G | 1.65677e-05 | 0.00287812 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157261 | TAACAGTGCTTCAGA[A/G]CAAAAATGAATCATT | 25831 |
rs768266549 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206608 | GCAGTCTTGGCAACT[A/G]TTCTTAAAAGTTAAA | 25831 |
rs768273458 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198950 | CTAAGGCGGGAGAAC[C/T]GCTTGAATCTAGGAG | 25831 |
rs768300106 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205501 | TATTTTCCCCAGTTC[A/G]TGACATATTTTGAAA | 25831 |
rs768344510 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148627 | GGGCTGCTTATGTTC[C/T]ATGGCTCAATTTTTT | 25831 |
rs768347192 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160756 | GCTCACTGCAGCCTC[A/G]ACCGCCCAGGCTCAA | 25831 |
rs768351598 | snp | C/T | 1.65806e-05 | 0.00287924 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139889 | TACATTTTTTATGGT[C/T]ACCTGGAGGTTATAT | 25831 |
rs768379626 | snp | A/C/T | 1.66112e-05 | 0.00288189 | missense | HECTD1 | GRCh38.p7 | 14:31107009 | TCACCTCGTGACTCA[A/C/T]AAATCAGTTTACTCA | 25831 |
rs768380299 | snp | A/G | 1.66518e-05 | 0.00288542 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157121 | TATTTCAGACTACTA[A/G]CTAAAGGAAATTAAT | 25831 |
rs768388315 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154053 | AAGAGTTGAAATTGA[C/T]GTATATCCTTCTACG | 25831 |
rs768394767 | snp | A/C | 1.66763e-05 | 0.00288753 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173602 | GATTACTCAATTTGG[A/C]ATCTGCAGTGGTGGA | 25831 |
rs768404553 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136681 | CTACACAAAAACGAT[C/T]AAAATACTCTGGAAA | 25831 |
rs768408652 | snp | A/G | 6.67167e-05 | 0.00577528 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149098 | GTATAGGTTGACTTG[A/G]AGTAGATGGCTTTAC | 25831 |
rs768420122 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120379 | CCGGGAGACAGAGTG[-/A]GGCTCTGTCTCAAAA | 25831 |
rs768438457 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186884 | AAAAATCAGCCGGAC[A/G]TGGTGGCACATGCCT | 25831 |
rs768443250 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138897 | CTTGCTAGGAAACAC[C/T]AAAAAACCCACAAAA | 25831 |
rs768454729 | snp | G/T | 6.63691e-05 | 0.00576022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109382 | TTCCCTAAATCTAAT[G/T]TTATATGAGATTACC | 25831 |
rs768477551 | snp | C/T | 2.21516e-05 | 0.00332796 | missense | HECTD1 | GRCh38.p7 | 14:31114334 | CTTCATTTCTCTGTA[C/T]ATGATTCTAAACATG | 25831 |
rs768479892 | snp | A/T | 1.66849e-05 | 0.00288828 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169490 | AAGAAAAGCATTTAA[A/T]TTGAATATAACAATA | 25831 |
rs768484703 | snp | G/T | 6.70196e-05 | 0.00578838 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173483 | TTATACAAAAACACT[G/T]TTTCTGAAGATTAAA | 25831 |
rs768493263 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126974 | CCACTTCTGACCAGA[-/T]TTTTTTTTTTTTTTT | 25831 |
rs768508813 | in-del | -/CACACCCG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104970 | AGTGTGAGCCACCAC[-/CACACCCG]CACACCCGACCACCA | 25831 |
rs768531677 | snp | A/G | 1.65781e-05 | 0.00287902 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148937 | ATGTTTGGTTCCTCT[A/G]TTAGATTCAAATACA | 25831 |
rs768560110 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31119078 | CTTGGCTCACTGCTC[A/G]TCGTCACTCTGACTC | 25831 |
rs768597524 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174665 | CTCAGTACAAGTACA[A/G]CTGTAAAAACATTTT | 25831 |
rs768614510 | in-del | -/T | 1.65627e-05 | 0.00287769 | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173369 | TATCAAGCACACATC[-/T]TTCATCACCCTGCAA | 25831 |
rs768623694 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152388 | AGAGACAGAGTTTTG[C/T]CATGTTACCTAGGCT | 25831 |
rs768659563 | snp | C/T | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099676 | CTATAAGCACAGATA[C/T]GGTAATAACTGGAAT | 25831 |
rs768662476 | snp | A/C | 3.80626e-05 | 0.00436232 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173770 | GGGTAAATCGGTCAG[A/C]CAGTGATGCAAAGCA | 25831 |
rs768669317 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198140 | ACTAGATGAAGCAAA[A/T]TTATTAAATTTACTA | 25831 |
rs768684364 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206194 | AAAACCAGTTTTGCA[C/T]AAGAGTATATAAGCT | 25831 |
rs768709642 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110250 | TTAACTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 25831 |
rs768715036 | snp | A/C | 1.65974e-05 | 0.0028807 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127989 | TAGGGAAACTCTGAG[A/C]ACCCATAAGAGGAGA | 25831 |
rs768742710 | snp | A/C | 3.31818e-05 | 0.00407306 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105370 | AATTATGCTAAAAAT[A/C]CTTTAAAATTACCTC | 25831 |
rs768789772 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31140972 | TCACTCTGTCACCTA[A/G]GCTGGAGTACGGTGG | 25831 |
rs768798124 | snp | G/T | 3.31719e-05 | 0.00407245 | missense | HECTD1 | GRCh38.p7 | 14:31112453 | ATGTGAAATAAAGCT[G/T]TCTAGTTTCAAATGG | 25831 |
rs768799370 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108905 | AACCAACAATGTCCA[C/T]AGTAACATTTCTAAA | 25831 |
rs768807382 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141679 | CAATGTTTCTTTTTA[G/T]TCCATTAGATTAAAA | 25831 |
rs768807815 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122365 | GCACTGGCTAAGTTC[A/G]TGTGTGTGCGCGCAT | 25831 |
rs768821636 | snp | A/T | 2.46594e-05 | 0.00351128 | splice-acceptor-variant | HECTD1 | GRCh38.p7 | 14:31141954 | TCCAAATCCATGCTC[A/T]AAAGAAAACAAAAAG | 25831 |
rs768864749 | snp | C/T | 5.00304e-05 | 0.00500127 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119659 | ACCCTACTTTTCATA[C/T]CTGATTTAGTATGTA | 25831 |
rs768871704 | snp | A/G | 1.66618e-05 | 0.00288628 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150228 | TTCATCTTCCTAAAT[A/G]TGTAGAATTATTCAA | 25831 |
rs768882078 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133982 | GGGTGGCTGAGGTGA[C/G]GGGAATCACTTGAGC | 25831 |
rs768912046 | snp | C/T | 1.65633e-05 | 0.00287774 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128951 | TTGCACTAGACTCCC[C/T]AGGAGTACGAACAGA | 25831 |
rs768926523 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198748 | TATGATATCAGAATC[C/T]ACATTATAACTAATC | 25831 |
rs768929235 | snp | C/T | 3.62799e-05 | 0.00425895 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135464 | CAGCTTAAAGTAAAA[C/T]GACTGACTTACTTTG | 25831 |
rs768986622 | snp | A/G | 1.76824e-05 | 0.00297336 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148677 | ACTGAAAATTTAACA[A/G]ATCAGTATAAAAGAC | 25831 |
rs768992356 | snp | A/G | 1.65949e-05 | 0.00288048 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173184 | TGCATCTATAAGTGC[A/G]TCGGTATCTTTACTT | 25831 |
rs768996702 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143022 | CACAAGGATGACACA[C/G]AAATTCGTGAAGCAT | 25831 |
rs769001457 | snp | C/G | 1.65649e-05 | 0.00287788 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150063 | AAGTTTTCCATCCAA[C/G]ATAAATCTGAACCAT | 25831 |
rs769038572 | snp | G/T | 3.31488e-05 | 0.00407103 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128803 | ATAGGGGCCCCAGCA[G/T]CCAACAAAGAACTCA | 25831 |
rs769042936 | snp | C/T | 1.66446e-05 | 0.00288479 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178243 | GCTGGTAAGAAAGTG[C/T]GAGGAGGACATCTGT | 25831 |
rs769072519 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206334 | ACACCTAACTAAAGG[C/T]TCTGTTTTTTCCAGC | 25831 |
rs769094467 | snp | A/G | 0.000298058 | 0.0122041 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134988 | TCCATAACCACGAGC[A/G]TGACGAAGTGTATAT | 25831 |
rs769120296 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193960 | AATATTTTTTAAAAG[C/T]TTATGTTCTCACACA | 25831 |
rs769125109 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199395 | GGTTTATTATTATAA[-/T]TTTTTTTTTTTTTTT | 25831 |
rs769130008 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116779 | GGGATTATAGGTGCC[A/C]AACACCACATCTGGA | 25831 |
rs769139604 | in-del | -/CAGATTGTGTCT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190431 | TGAACTCACCGAGTC[-/CAGATTGTGTCT]TAGCTTTTTTCTGAG | 25831 |
rs769144601 | snp | C/T | 1.66114e-05 | 0.00288192 | missense | HECTD1 | GRCh38.p7 | 14:31106971 | AAGCTTCAGACTGAC[C/T]TTCAGTACAGTGTAA | 25831 |
rs769230837 | snp | A/G | 1.74479e-05 | 0.00295358 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178269 | TCTGTAGTGAAAGAA[A/G]TCATATTACATCTAG | 25831 |
rs769240619 | in-del | -/AAC | 3.31208e-05 | 0.00406931 | cds-indel, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129087 | TTCAGCAGATGAAAG[-/AAC]AACAATTGGTTCATG | 25831 |
rs769247690 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145624 | TGCAGTGAGCCAAGA[C/T]TGTGCCAGTGCCTGG | 25831 |
rs769249933 | snp | A/G | 1.65608e-05 | 0.00287752 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122901 | TGTAAAGAGAATGGG[A/G]TACTCTCTCTACCAT | 25831 |
rs769259996 | snp | C/G | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178056 | GTCTCTGCTAGTCCT[C/G]TTGTTAAGTTCAACT | 25831 |
rs769266576 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31114544 | AGTTTCAAACTCCTG[A/G]TTTCAAGCGATGCTC | 25831 |
rs769269278 | snp | A/C | 1.7564e-05 | 0.0029634 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113828 | AAAGCTGCAAAACAA[A/C]GCACGAAGCCATTTG | 25831 |
rs769273496 | snp | A/T | 3.31857e-05 | 0.00407329 | missense | HECTD1 | GRCh38.p7 | 14:31106778 | CTCTTGATAGCAAGG[A/T]CTTTAATTTCTTTTA | 25831 |
rs769288373 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194957 | TATCTGTAGTAGAGA[C/T]ATTTTATAAAATAGT | 25831 |
rs769330648 | in-del | -/ATA | 4.97673e-05 | 0.00498811 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119895 | ATTTCACACACAAAC[-/ATA]ATAAGATGCAAAATT | 25831 |
rs769358709 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194002 | TATACACTACTGTTT[A/G]TAGCAGTTTAGGTCA | 25831 |
rs769374081 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127141 | CACGCCCAGCTAATT[G/T]TTTTTATATTTTTAG | 25831 |
rs769377395 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164596 | CCTCACCTTGGAGAC[A/G]AGCCAATTGATTAAG | 25831 |
rs769387867 | snp | C/T | 1.66092e-05 | 0.00288172 | missense | HECTD1 | GRCh38.p7 | 14:31107000 | AAGTCTCTATCACCT[C/T]GTGACTCATAAATCA | 25831 |
rs769399672 | snp | C/T | 5.17469e-05 | 0.00508633 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173721 | TCCTCAGTTAATCCA[C/T]GCTTGGCTAATGGAG | 25831 |
rs769399791 | snp | C/T | 1.69444e-05 | 0.00291066 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148709 | AGAATAAAGCACATC[C/T]AACAGATATACCTTT | 25831 |
rs769411564 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189362 | TCCTAACCAGAATCT[C/G]TCACTAGATTCTCCA | 25831 |
rs769428641 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149365 | ATCACTTGAGCTCAC[A/G]AGTTTGAGGCTGCCA | 25831 |
rs769479423 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174523 | CACTCCACCCTGGGT[-/A]GACAGATCAAGACTC | 25831 |
rs769488285 | snp | A/G | 0.000263961 | 0.0114853 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133216 | CCCATTTTCTACACA[A/G]AAGTGCTGAGCACCT | 25831 |
rs769515503 | snp | C/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208294 | AAGAGGTGCTGCCGA[C/G]GATTATCAACGTTGT | 25831 |
rs769522373 | snp | A/G | 6.62482e-05 | 0.00575497 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168364 | AACCTTTTCAAGTAT[A/G]TGGGTGCCATTTCCG | 25831 |
rs769560642 | snp | A/C | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173679 | CCTGAAACAGTACCA[A/C]CAGCAGCAGCCATTC | 25831 |
rs769574276 | snp | C/G | 1.6599e-05 | 0.00288084 | missense, utr-variant-5-prime, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157287 | TCATTTTTCGAATTA[C/G]AGCAAGACTTGCTTT | 25831 |
rs769574750 | snp | C/T | 1.66832e-05 | 0.00288814 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173627 | GGTGGATGGAGCTCC[C/T]GTGGTGCTGCGACCT | 25831 |
rs769580685 | snp | C/G | 1.65616e-05 | 0.00287759 | missense | HECTD1 | GRCh38.p7 | 14:31102971 | TAATATCCTCTGCTG[C/G]CCAGGATGGTGACTG | 25831 |
rs769583357 | in-del | -/TTTCAG | 3.32215e-05 | 0.00407549 | cds-indel | HECTD1 | GRCh38.p7 | 14:31106971 | AAGCTTCAGACTGAC[-/TTTCAG]TACAGTGTAAGTCTC | 25831 |
rs769599870 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144003 | ATTAACATCATTCAG[C/T]TTTTAAATATTTCTT | 25831 |
rs769605657 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125661 | TTTTGCTACACACAC[A/G]TTTAATAAGCAGAAA | 25831 |
rs769612043 | snp | A/C/G | 9.94685e-05 | 0.00705162 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129375 | CCCTGGTGCAAGCTT[A/C/G]AGGTCAAATTTTCCT | 25831 |
rs769664905 | snp | A/T | 1.77694e-05 | 0.00298067 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140049 | AACTACATGTAAATG[A/T]TCATGCAGAAAATAT | 25831 |
rs769675972 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202817 | GACTACTGGCTGGGC[A/C]TGGTGGCTCACACCT | 25831 |
rs769692321 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177903 | AATTTTTTTTTTTAG[A/T]AATTTTTTTTTTTTA | 25831 |
rs769696805 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108713 | AGGAGGAATACAATG[A/G]AAGTCTGTATATAAA | 25831 |
rs769711488 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129408 | TGCGCCCATACGGTA[A/G]GAGTTTGAGCCACCA | 25831 |
rs769714931 | snp | C/G | 1.67975e-05 | 0.00289802 | missense | HECTD1 | GRCh38.p7 | 14:31109561 | TTCTCGTTCGCTCCA[C/G]AGTGGCTTCACGTCG | 25831 |
rs769718679 | in-del | -/AACT | 1.92927e-05 | 0.0031058 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156802 | CAAAAAAAAAAAAAA[-/AACT]AACTCTTCCTGATAC | 25831 |
rs769739704 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144735 | TACTCAATACCCATG[A/G]CATAAAGGATAGAGG | 25831 |
rs769768197 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195454 | TACCCATAAATAAAA[A/C]TGATAAAAATCTATC | 25831 |
rs769783967 | snp | A/G | 0.000133826 | 0.00817895 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107714 | TTCAACCTAAAATAT[A/G]AACAAATAAATTGTG | 25831 |
rs769789277 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139191 | TGCTTAAAATATCTT[C/G]ACTTTTTTTCTTATG | 25831 |
rs769796478 | snp | A/C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188202 | AAAATCCTTTTCCCC[A/C/T]AACTCTTTCCAAAGC | 25831 |
rs769837274 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155396 | TTTACAGTAGAGAAA[A/C]CTGGAAGAGAAAAAC | 25831 |
rs769839072 | snp | C/T | 1.6569e-05 | 0.00287824 | missense | HECTD1 | GRCh38.p7 | 14:31116387 | TTCCAAGACCTGTTA[C/T]TTTCAAAGTGAGAGC | 25831 |
rs769841043 | snp | C/T | 4.96907e-05 | 0.00498426 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31109409 | TACCTCAAGAACTGA[C/T]TTCCGATCTGCATGT | 25831 |
rs769863013 | snp | C/T | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100335 | CTTTGATCTTCATAG[C/T]ATGGCATTTAGGAAA | 25831 |
rs769891893 | snp | A/G | 3.31362e-05 | 0.00407026 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116280 | TTTATCTGATTTCAC[A/G]TTGCCATTACAGGAC | 25831 |
rs769900829 | snp | A/G | 1.66601e-05 | 0.00288614 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169323 | GAAAAATAACAGTAG[A/G]TGGCTTCAAAAGAAA | 25831 |
rs769948264 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111635 | TTGGTTTTCACACAG[C/T]GCGCTTCTCTGGGTG | 25831 |
rs769971819 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129086 | TTTCAGCAGATGAAA[C/G]AACAACAATTGGTTC | 25831 |
rs769975591 | snp | A/G | 7.6063e-05 | 0.0061665 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141981 | AAAGTATAAAGTCCA[A/G]AAAAAAATAATTTAA | 25831 |
rs769986930 | snp | C/G | 1.70351e-05 | 0.00291843 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112591 | TATAAGGCATTCATG[C/G]ATGCATGCATTCATT | 25831 |
rs769998858 | snp | A/G | 1.9214e-05 | 0.00309945 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144104 | CTTTACTACTTGATA[A/G]ACTTACATTGTTTAA | 25831 |
rs770013140 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152442 | CGACCTGTCCGCCTC[A/G]GCCTCCCAAAGTGCT | 25831 |
rs770022695 | snp | A/T | 1.6599e-05 | 0.00288084 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133532 | TCTTCACATACTCCA[A/T]TTACAGTGCCATAAA | 25831 |
rs770030585 | snp | A/G | 1.66424e-05 | 0.0028846 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150242 | TGTGTAGAATTATTC[A/G]ATTAAACATGGAAAA | 25831 |
rs770040342 | snp | C/T | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119796 | ACCAATGCAGAAAAC[C/T]GTCTCTTTAGCACAT | 25831 |
rs770057008 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31128079 | AAACCAAGTTTTTTA[-/T]TTTTTTAAAGAGTGA | 25831 |
rs770079178 | snp | C/G | 1.66275e-05 | 0.00288331 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133390 | TGCCGTCTAAGATTA[C/G]CTTCTGCTTCTTTAG | 25831 |
rs770081924 | snp | A/G | 3.31219e-05 | 0.00406938 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129044 | TGCTTGCACTGGAAG[A/G]TGACCCTACTTCTGT | 25831 |
rs770096007 | snp | A/G | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173289 | TGTAGATCCAGCACT[A/G]GACTTTGGCAAAGCT | 25831 |
rs770100176 | in-del | -/GTGCGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134566 | TGTGTGTGTGTGTGT[-/GTGCGC]GCGTATGTATATACA | 25831 |
rs770111442 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193795 | CGGGCATGGTGGCGG[A/G]CACCTGTAATCCCAG | 25831 |
rs770119522 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31143270 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCAGG | 25831 |
rs770160735 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191702 | ACCCCAGCTTTCACT[C/T]AAGAAAACAGAGAAG | 25831 |
rs770163230 | snp | C/T | 1.66668e-05 | 0.00288672 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119671 | ATATCTGATTTAGTA[C/T]GTATTAAAATTAAAT | 25831 |
rs770165556 | in-del | -/TGTGCG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134565 | GTGTGTGTGTGTGTG[-/TGTGCG]CGCGTATGTATATAC | 25831 |
rs770177934 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110547 | GCATTAAATGGTACA[A/C]AAATGTAACTATCAG | 25831 |
rs770205448 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158965 | AAACAAACAAACAAA[A/C]AAAAGGCTTGTCTAT | 25831 |
rs770223962 | snp | A/G | 1.6566e-05 | 0.00287797 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101070 | CAGTAGCATCAACCT[A/G]CAACAAGAAAGCAAA | 25831 |
rs770252386 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182196 | ACTGCGCCCAGCCTC[-/T]TTTTTTTTTTTCCAG | 25831 |
rs770257208 | snp | G/T | 1.65718e-05 | 0.00287848 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173201 | CGGTATCTTTACTTC[G/T]AATACAATCTATAAG | 25831 |
rs770288826 | snp | C/T | 1.65655e-05 | 0.00287793 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173221 | CAATCTATAAGCTGC[C/T]GATGTGAGCGCTCCC | 25831 |
rs770309354 | snp | C/T | 1.66366e-05 | 0.0028841 | missense | HECTD1 | GRCh38.p7 | 14:31107163 | TGATCCTTTCAAGCT[C/T]ATCACTATCCTGTGG | 25831 |
rs770313203 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195526 | AGAGTGGTTTTTAAC[-/T]TTTTTTTTTTTTGAG | 25831 |
rs770340658 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202390 | TATCCCATTGCAGAG[A/G]CCACTGTTTCTACCA | 25831 |
rs770345112 | snp | C/G | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205824 | CGATCCACGTTGTCA[C/G]ACATCAAAAGCAGCA | 25831 |
rs770378300 | snp | A/G | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205853 | CATGCATAGCTGTTC[A/G]AGGGCTATTAGTTGC | 25831 |
rs770410799 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104328 | AAAAAATACCCATTA[A/C]CGATGAAATGGACAG | 25831 |
rs770435912 | snp | C/T | 1.65789e-05 | 0.0028791 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148818 | GGGGAAAAAAAAGAA[C/T]ATTCACAGAGCTTAC | 25831 |
rs770441508 | snp | C/T | 4.77236e-05 | 0.00488462 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114272 | GAGTAAACCAATGTT[C/T]TAAAATAACTTACCA | 25831 |
rs770475133 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31184753 | TTAAAAAATATATGT[A/C]TACACAGACATACAC | 25831 |
rs770500581 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103709 | AAGGTGGCTCACACC[C/T]GTAATCTCAGCACTT | 25831 |
rs770500880 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116513 | AACAAGCAGTCCAAG[A/G]AAGGCCACTACACTA | 25831 |
rs770527251 | in-del | -/A | 2.46917e-05 | 0.00351358 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114242 | TATCTTTCTTCTTTT[-/A]AACTAAATAGCCAAG | 25831 |
rs770540837 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135730 | TTATTATAACAAATG[C/T]TCATTTAGGCCGGGT | 25831 |
rs770555933 | snp | A/G | 1.65836e-05 | 0.0028795 | stop-gained, intron-variant | HECTD1 | GRCh38.p7 | 14:31113981 | CGTCTGCATTCTTCT[A/G]CAGGTAGGTTATCAA | 25831 |
rs770557051 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31106190 | AAAGGCCTTGCAGTT[A/C]ACCTAAAATCACAGC | 25831 |
rs770610928 | snp | A/C | 1.66161e-05 | 0.00288232 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123065 | TGAAAACAAAACCCA[A/C]AACCTTATGTCAACA | 25831 |
rs770619113 | in-del | -/GAT | 0.000115958 | 0.00761352 | cds-indel | HECTD1 | GRCh38.p7 | 14:31109518 | CTCGAAACTCTCCAG[-/GAT]GGTCATCTCGCCTAA | 25831 |
rs770644422 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31164741 | CTGCTAATAACTACC[C/T]GGGAAAATTTAGCAT | 25831 |
rs770653648 | snp | A/C | 1.7213e-05 | 0.00293364 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135493 | TGCATTTGTTCCAAT[A/C]CAGTAAATGATTCCA | 25831 |
rs770658851 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165701 | CAGTAAATATCTACT[A/G]AGGACCTAAGGATCA | 25831 |
rs770677862 | snp | C/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209647 | GCTCACACCCGTAAT[C/G]CCAGCACTTTGGGAG | 25831 |
rs770718205 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163767 | CTACAAAAATTAGCC[A/G]GGCATGGTGGTGCGT | 25831 |
rs770731798 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115764 | CAACAGAGAGAGACC[C/T]TGTCTCAGAAAAAAA | 25831 |
rs770738758 | snp | C/T | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168374 | AGTATATGGGTGCCA[C/T]TTCCGGATCTCCTTT | 25831 |
rs770815904 | snp | A/T | 0.000156638 | 0.0088484 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116497 | AAAACAATTATACTA[A/T]AACAAGCAGTCCAAG | 25831 |
rs770821753 | snp | C/G | 3.63247e-05 | 0.00426157 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173751 | GCTGGGTCAACACCA[C/G]GACGGGTAAATCGGT | 25831 |
rs770858091 | snp | A/G | 1.66065e-05 | 0.00288149 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105352 | TCAAAGTGAAAGGAG[A/G]GCAATTATGCTAAAA | 25831 |
rs770881460 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132126 | AGTACCGTCACATTT[A/T]TTCTAGCTCTTTAAA | 25831 |
rs770881677 | in-del | -/AG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156620 | CTAGTGAATTTGGAT[-/AG]AGAGTATTCTGATAT | 25831 |
rs770971651 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141507 | AAGACAGGAGAAATG[A/C]TTGAGCCCAGGAGGT | 25831 |
rs770981024 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120788 | CTACTATTACATGTA[C/T]GACTTTTAGCAATTA | 25831 |
rs771005504 | snp | A/C/T | 4.97462e-05 | 0.00498708 | missense | HECTD1 | GRCh38.p7 | 14:31106760 | TTGCTTAAAATTTGG[A/C/T]GCCTCTTGATAGCAA | 25831 |
rs771024938 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117866 | TGTTTTCCTTTTTTA[C/T]AATTCATTTTTTTTC | 25831 |
rs771033821 | in-del | -/A | 1.67683e-05 | 0.00289549 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173510 | AAAAAGCAAAGATTC[-/A]AAAAACATTCTTACA | 25831 |
rs771067708 | snp | A/C | 1.68709e-05 | 0.00290434 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128018 | GAAGCTAAAGACAAA[A/C]ATGAAGCAAATCAGT | 25831 |
rs771121143 | snp | A/G | 1.67049e-05 | 0.00289002 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134880 | AACTAACCCTGGTTC[A/G]TTGAGACTGCAGTCA | 25831 |
rs771124367 | in-del | -/GTGTGTGTGTGTGTGTGCGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134552 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGCGC]GCGTATGTATATACA | 25831 |
rs771143656 | snp | C/T | 1.6851e-05 | 0.00290263 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169513 | TAACAATACTTTATT[C/T]CTTTGACATCCAACT | 25831 |
rs771143986 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190882 | GTCTCCGACTCCTGG[A/C]CTCAAATGATCCTCC | 25831 |
rs771173717 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111714 | CCTTCTTTTTCTGAT[C/T]ATTTTCCTTCATGTG | 25831 |
rs771179391 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118654 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGTGGGTA | 25831 |
rs771201605 | snp | C/T | 2.23646e-05 | 0.00334392 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144295 | GAAGGCAATCAAAAA[C/T]ATAAACATAGCTCTT | 25831 |
rs771212525 | snp | A/G | 1.66765e-05 | 0.00288756 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121334 | TGGTGCTTTACTATA[A/G]AAGGGAAAAATATAC | 25831 |
rs771228711 | snp | A/C | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100461 | CATCATTAAAAAGGA[A/C]AAGAAAAAGCTTGAG | 25831 |
rs771246315 | snp | A/T | 5.01794e-05 | 0.00500871 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178014 | GAGCCAATAAGTAAT[A/T]CTTACCTTTACACAC | 25831 |
rs771255009 | snp | A/C | 1.81602e-05 | 0.00301326 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144123 | TACATTGTTTAACAC[A/C]GTAAGAAGTGCTTGT | 25831 |
rs771255093 | snp | A/G | 0.00010326 | 0.00718464 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157031 | AAATAAAAAATAAAA[A/G]TAAGTTTAGTTGCCA | 25831 |
rs771257353 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108674 | ATTAAAAAAAAAAAA[A/G]AAGAAGAAGAAGAAC | 25831 |
rs771270241 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205036 | AATTACTTATTACTG[A/G]AGTTCAAAACTGTAA | 25831 |
rs771285694 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145081 | CACAAATGAGCTCTC[A/G]AAGTTACAGTTATTT | 25831 |
rs771321425 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137247 | GCAATTCTCCTACCT[C/T]AGCCTCCTGAGTAGT | 25831 |
rs771331028 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186450 | CCCAGCACTTTGGGA[A/G]GCCGAGCCGGGTGGA | 25831 |
rs771331863 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179812 | CTCAACATTTTAATG[A/G]AATAATTTATCTTCC | 25831 |
rs771339826 | snp | A/C | 4.17005e-05 | 0.00456602 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113055 | AAGGGAATATTAGGA[A/C]AAGTCCAACAGTAAT | 25831 |
rs771366807 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191765 | GCACTTTGGGAGGTC[A/G]AGGCAGGCGGATCAC | 25831 |
rs771373985 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204123 | GTGTATATGTGCCAC[A/G]TTTGCTTAATCCAGT | 25831 |
rs771379436 | snp | A/G | 0.000103219 | 0.00718322 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156847 | CCACTCACTTTTTCT[A/G]GTTTTGATTCCTCTT | 25831 |
rs771393551 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124406 | GTGCCTGCGGTAAGA[C/G]AAAAACCACAAAACA | 25831 |
rs771449905 | snp | C/G/T | 4.96967e-05 | 0.00498461 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101088 | ACAAGAAAGCAAACA[C/G/T]AACAGAAGACCATGA | 25831 |
rs771464276 | snp | C/T | 1.65619e-05 | 0.00287762 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119820 | AGCACATAATCATCA[C/T]CCCATGTTCTCCGGC | 25831 |
rs771467469 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159287 | CAGAGGACAAACTGT[C/T]CTAACAGGATTGGTT | 25831 |
rs771522058 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193287 | GTTAAACTTACTGCA[C/T]ATGGATATCCAATTG | 25831 |
rs771524546 | snp | A/G | 1.65869e-05 | 0.00287979 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101279 | TGCTTTCCTTTCATC[A/G]GAAGACATGCCACAT | 25831 |
rs771534036 | snp | A/C | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173300 | CACTAGACTTTGGCA[A/C]AGCTTTTCGTCCTTC | 25831 |
rs771544204 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171698 | GTTTTTATTGAATCT[A/G]TATTAGGAAACACTA | 25831 |
rs771557279 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105283 | TGGGATTACAGGTGT[A/G]AGCCACCGTGCCCAG | 25831 |
rs771558356 | snp | A/G | 1.67267e-05 | 0.0028919 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173467 | GTTTAATATATTAGC[A/G]TTATACAAAAACACT | 25831 |
rs771565983 | snp | C/T | 6.62789e-05 | 0.00575631 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136671 | TTGTAAGTATCTACA[C/T]AAAAACGATCAAAAT | 25831 |
rs771568176 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105674 | GAAATTTAAACTGGG[A/C]GGACAAAAAAGATTA | 25831 |
rs771575812 | snp | A/C | 1.65663e-05 | 0.002878 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101091 | AGAAAGCAAACACAA[A/C]AGAAGACCATGAGTT | 25831 |
rs771590581 | snp | A/G | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173362 | CGCATAGTATCAAGC[A/G]CACATCTTTCATCAC | 25831 |
rs771613394 | in-del | -/TAAGTT | 3.31474e-05 | 0.00407095 | cds-indel | HECTD1 | GRCh38.p7 | 14:31116261 | GCTCCCAAATACGCC[-/TAAGTT]TATCTGATTTCACAT | 25831 |
rs771616409 | snp | C/T | 8.28e-05 | 0.00643375 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129068 | CTTCTGTTTGAGGGA[C/T]GTTTTCAGCAGATGA | 25831 |
rs771628008 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208881 | GATAATGCCACCTCA[C/T]TCCAGCCTGGGCGAC | 25831 |
rs771628342 | snp | C/G | | | intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31123594 | TTGTCCTGCATAAAT[C/G]AAGATGCTGACAAAC | 25831 |
rs771665721 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133180 | AATTTATAAATTATC[C/T]TAAAAGAAAAAATTT | 25831 |
rs771686678 | snp | A/G | 8.2958e-05 | 0.00643988 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148900 | CTACATACTTACCCA[A/G]GGAAGTTTCTGCAGT | 25831 |
rs771689513 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31123758 | AAGAACATCCAGAAG[A/C]CAATTTATAATTGCT | 25831 |
rs771692838 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108840 | CCCCTGTGACAGGAG[-/A]ACGTATTTCCACTCT | 25831 |
rs771702779 | snp | A/G | 1.66527e-05 | 0.00288549 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107552 | CTCAAGTCACAAAAT[A/G]AGAAATATTCTTACG | 25831 |
rs771740774 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124628 | GCGACTCCAAAAGGA[C/G]TGCAAGAGTGGGCAA | 25831 |
rs771795011 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117566 | TTTTTATTAGCTCAT[C/G]AATGTTTTCTTCATT | 25831 |
rs771816223 | snp | C/G | 1.65756e-05 | 0.00287881 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136518 | TTTCACCGTGCCCTT[C/G]CCAGAAACTCACCAT | 25831 |
rs771816653 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31197539 | GAATATCAAGCTTCA[C/T]ATAAGACCAACTGAA | 25831 |
rs771829086 | snp | A/T | 1.66106e-05 | 0.00288184 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169476 | AACAGAGTCTAGAGA[A/T]GAAAAGCATTTAATT | 25831 |
rs771872992 | snp | A/G | 6.63592e-05 | 0.00575979 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148840 | AGAGCTTACTTTGTT[A/G]CAATTTAACATATTC | 25831 |
rs771873539 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186822 | ACTTGAGGCAAATTC[A/G]AGACCAGCCTGGCCA | 25831 |
rs771877362 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116611 | GACTCTCTAGGCGTC[A/G]ACATTTTTGCTTTCT | 25831 |
rs771878145 | in-del | -/GTC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125829 | CTTCACATAAACTTT[-/GTC]TTTAAAATTACTCCC | 25831 |
rs771878279 | snp | A/G | 1.66114e-05 | 0.00288192 | synonymous-codon, intron-variant | HECTD1 | GRCh38.p7 | 14:31114024 | TAATTCATCAGTGCC[A/G]AGGTACTGCTCCACA | 25831 |
rs771884734 | snp | A/G | 1.6577e-05 | 0.00287893 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105552 | TTGCTAAGAGGATAT[A/G]TCAGAACTTACAACT | 25831 |
rs771920399 | snp | A/G | 4.96857e-05 | 0.00498401 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127840 | ACTGGAAGTTGATGT[A/G]AGGCTGGTGGTTAAA | 25831 |
rs771930497 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104588 | AAAAGTAATTTACCT[G/T]GTAATATACTTTGTT | 25831 |
rs771952040 | snp | A/C | 1.69046e-05 | 0.00290723 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168498 | ATATTTTTTAAAGAA[A/C]TACTTTTTTGGAAAC | 25831 |
rs771990279 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154980 | TGAATACAGAAATTG[A/G]TGGGTTAAATTTACT | 25831 |
rs771992544 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176474 | AATATGGTAAATAAA[C/T]AGACAAAACCTATAT | 25831 |
rs771997772 | snp | A/G | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100223 | ATACAAAGAAAATAC[A/G]ACCGAAAGTAAAACT | 25831 |
rs772060392 | snp | C/T | 3.32452e-05 | 0.00407695 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31174929 | ATGATCTTCATGCTT[C/T]AATAAACTAGACAGA | 25831 |
rs772063126 | in-del | -/TG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198204 | TCTACTTAAAGGAAA[-/TG]TGGGAATTAATTATA | 25831 |
rs772064028 | snp | A/T | 1.66768e-05 | 0.00288758 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133500 | AAAAGCCTCGTATCA[A/T]CTCTTTACCTAGCTG | 25831 |
rs772075051 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108781 | TATCATATTTCTTGC[A/G]ATTAGTTTATGATCC | 25831 |
rs772095638 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200492 | CTCCATCTAATTTAA[-/A]AAAAAAAAAAAAAAA | 25831 |
rs772098672 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181203 | TTTAAGAGCAATGCT[C/T]AGTATAAACTTAATA | 25831 |
rs772124816 | in-del | -/C | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163898 | GCCTGGGTGACAGAG[-/C]CAAGACTCTGTCTCA | 25831 |
rs772165638 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31107746 | GTTAAACGTAAAGTT[G/T]GGGGTGTTTTTAAAA | 25831 |
rs772186423 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152855 | GCTGAGCATGGTGGT[A/G]TGCACCTGTAATTCC | 25831 |
rs772194444 | snp | C/G/T | 4.98288e-05 | 0.00499122 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133378 | ACTAGACGTCTCTGC[C/G/T]GTCTAAGATTAGCTT | 25831 |
rs772213029 | in-del | -/GTGTGTGTGTGTGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134556 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGC]GCGCGTATGTATATA | 25831 |
rs772227527 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155550 | ATAAGCTGAATTTAA[C/T]CACAAAGAAACATGA | 25831 |
rs772232439 | snp | A/G | 6.91061e-05 | 0.00587778 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128046 | AGTACAAATAGGTGA[A/G]ATTGTAGAAACCTCA | 25831 |
rs772236049 | in-del | -/A | 0.00315222 | 0.0395749 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172137 | CTGAAATTTTGAAGG[-/A]AAAAAAAAAGAAACG | 25831 |
rs772251839 | snp | A/G/T | 3.31281e-05 | 0.00406978 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150042 | ACCACTTGAATACAT[A/G/T]GTGGCAAGTTTTCCA | 25831 |
rs772259130 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31180113 | AACCTGGGAGGTGGA[C/G]GTTGCAGTGAGCTGA | 25831 |
rs772269848 | snp | C/T | 1.65701e-05 | 0.00287833 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128719 | GCTATGTTTGCCACT[C/T]TCCTTACAAAACTCT | 25831 |
rs772289440 | snp | C/T | 0.00014923 | 0.00863671 | missense | HECTD1 | GRCh38.p7 | 14:31106766 | AAAATTTGGCGCCTC[C/T]TGATAGCAAGGTCTT | 25831 |
rs772294541 | snp | A/G | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156943 | AGCTGATCCAAAAAT[A/G]TATCACCACCTTTAT | 25831 |
rs772300396 | in-del | -/AT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139046 | ATTATATACAGATAT[-/AT]ATATATATATATCTG | 25831 |
rs772323803 | in-del | -/A | 1.6593e-05 | 0.00288031 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148882 | CCAATAAACTTACAT[-/A]ATCTACATACTTACC | 25831 |
rs772325047 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181716 | ATCAGATTTTAATTG[C/T]GATCAACTGTGTTCC | 25831 |
rs772340143 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133813 | TCAACAGTTCATTAC[A/T]AGAATCAAGAAATCA | 25831 |
rs772374175 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199135 | AGCATATCCATGATT[A/G]CGTTAAAAAATATAA | 25831 |
rs772392792 | snp | A/C/T | 0.000101498 | 0.00712318 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144914 | CTTTAAAATGGTCAT[A/C/T]GTATAAATCTCGAGC | 25831 |
rs772402471 | snp | C/T | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119494 | AATACAAAACACATG[C/T]TGGTTTTTAAAATTT | 25831 |
rs772405672 | in-del | -/A | 1.69146e-05 | 0.0029081 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112390 | AAGCATACTTATTCT[-/A]AAAACATAAAAAAAA | 25831 |
rs772416800 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193815 | TGTAATCCCAGCAAC[C/T]TGGGAGGCTGAGGCA | 25831 |
rs772430550 | snp | A/G | 1.67567e-05 | 0.00289449 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171985 | ATAACGAATCATAAA[A/G]CTGCTTTTTATTAAT | 25831 |
rs772458480 | snp | C/T | 1.65888e-05 | 0.00287996 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134902 | CTGCAGTCATCAACA[C/T]GGGTATACAAAGAAG | 25831 |
rs772493891 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161306 | AAAGTAAGCCAGGCA[C/T]AGTGGCTCACGCCTG | 25831 |
rs772546055 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103582 | TTCATTTGTAGGAAC[A/G]TGGGTGGAACTGGAG | 25831 |
rs772552201 | in-del | -/TACTTCTTTAGAAAAAGAACCAGTATTTTGGAAATGACAAATTTG | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208951 | TTCTTTCTTTTTTAC[lengthTooLong]TACTTCAGATAGCTA | 25831 |
rs772586914 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194978 | ATAAAATAGTCTGTA[A/T]ATCAGGCACTTCATT | 25831 |
rs772628960 | snp | A/G | 1.69012e-05 | 0.00290694 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113239 | AAACTGACTTGCTTT[A/G]AAACTGCTATAGAAA | 25831 |
rs772642072 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183898 | TTTTTGGTAGAGACA[A/G]GTTCTTGCTATGTTG | 25831 |
rs772663891 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120339 | CAGTGAGCCGAGATC[A/G]TGCCACTACACTCTG | 25831 |
rs772688850 | snp | G/T | 2.03859e-05 | 0.00319258 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172168 | TATTTTTAAAGCCAA[G/T]AAAATACTAAACTTT | 25831 |
rs772704045 | snp | C/T | 1.65767e-05 | 0.00287891 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121455 | AACAGCATGATGCGT[C/T]ACATCAGAGCGGGAG | 25831 |
rs772706843 | snp | C/T | 1.73788e-05 | 0.00294772 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157061 | AGGAGTAGAGAAATG[C/T]AGTAATTTGCACAAC | 25831 |
rs772740373 | snp | C/G | 1.65647e-05 | 0.00287786 | missense | HECTD1 | GRCh38.p7 | 14:31113412 | CTTTTGTTAAATTAA[C/G]AATATCACTACTTTG | 25831 |
rs772743407 | snp | C/T | 1.66106e-05 | 0.00288184 | missense | HECTD1 | GRCh38.p7 | 14:31107007 | TATCACCTCGTGACT[C/T]ATAAATCAGTTTACT | 25831 |
rs772755340 | snp | A/G | 1.66269e-05 | 0.00288326 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121363 | ACATATGGTAGGGAA[A/G]ATAAACATGAAGATA | 25831 |
rs772776717 | snp | C/T | 0.00010482 | 0.00723872 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178271 | TGTAGTGAAAGAAAT[C/T]ATATTACATCTAGGG | 25831 |
rs772789762 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134235 | TATCAAATGCCAAAA[A/G]CAATTTGGGTACATA | 25831 |
rs772789986 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149773 | CCGGGCATGGTGACA[A/G]GTGCCTGTAGTCCCA | 25831 |
rs772804037 | snp | A/G | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178244 | CTGGTAAGAAAGTGC[A/G]AGGAGGACATCTGTA | 25831 |
rs772829605 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102861 | TTAGAGAATCTGTCA[C/T]TTGATTTGGGGAATA | 25831 |
rs772847091 | snp | A/T | 1.76993e-05 | 0.00297478 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135476 | AAATGACTGACTTAC[A/T]TTGCATTTGTTCCAA | 25831 |
rs772854185 | snp | G/T | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122932 | AACCTCCTCGTATTC[G/T]TGGTCCTCCTGATTG | 25831 |
rs772872587 | in-del | -/TA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174147 | TTTGTCATGATAATC[-/TA]TGATATCAACTGAAA | 25831 |
rs772887598 | snp | C/T | 0.00018354 | 0.0095779 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173635 | GAGCTCCTGTGGTGC[C/T]GCGACCTGGTTTGCA | 25831 |
rs772890044 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149344 | TTGGGAAGCTAAGGC[A/G]AGATGATCACTTGAG | 25831 |
rs772894407 | in-del | -/TTTC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122735 | ATATAAGCAACTTAT[-/TTTC]TTTAAGTGGAGAATC | 25831 |
rs772900266 | snp | A/G | 1.68838e-05 | 0.00290544 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148711 | AATAAAGCACATCCA[A/G]CAGATATACCTTTTG | 25831 |
rs772909298 | snp | A/C | 1.65647e-05 | 0.00287786 | missense | HECTD1 | GRCh38.p7 | 14:31102999 | CTGGTTTCCACAAAG[A/C]ATCATTTGGACTTCT | 25831 |
rs772948905 | snp | C/T | 4.96857e-05 | 0.00498401 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168365 | ACCTTTTCAAGTATA[C/T]GGGTGCCATTTCCGG | 25831 |
rs772953422 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31194200 | GAAAAGTCAAAACTA[C/T]ATCAACAGAAAACAG | 25831 |
rs772964807 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154927 | TAGACACAGAAAAGG[-/T]TATATTTAAATTTGC | 25831 |
rs772968570 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202199 | GCGAGACTCTGCCTC[-/A]AAAAAAAAAAAAAAA | 25831 |
rs772969412 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102725 | GTGAGCCACCGCGCC[C/T]GGCCTGCTGTCAGTT | 25831 |
rs772975786 | snp | C/G | 1.65825e-05 | 0.00287941 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121485 | GCCAGCTCGACGTTG[C/G]AGGGATGGGCGTCTC | 25831 |
rs773025663 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147873 | TCCCCTAATCCTAAT[C/T]ATATACAAGTATTCT | 25831 |
rs773027749 | snp | A/G | 1.6985e-05 | 0.00291414 | stop-gained, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144926 | CATCGTATAAATCTC[A/G]AGCCATAGTTCGTAC | 25831 |
rs773028168 | in-del | -/AC | 1.93168e-05 | 0.00310773 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156804 | AAAAAAAAAAAAAAA[-/AC]TCTTCCTGATACCTC | 25831 |
rs773042563 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31140092 | CAATATATACCCCTA[A/C]TTTTTCATGACTACA | 25831 |
rs773098392 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188331 | ACCTCTGCCTCCTGC[A/G]TTCAAGCGATTCTCT | 25831 |
rs773151512 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189420 | CCAAAGATATATTTT[C/T]AAAACACAAATCTGT | 25831 |
rs773153502 | snp | A/G | 0.000234125 | 0.010817 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173525 | CAAAAACATTCTTAC[A/G]TGTGTTACTACCGGA | 25831 |
rs773153674 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125075 | CCTCCCAAAATGCTG[A/G]GATTATAGGCGTGAG | 25831 |
rs773208064 | snp | C/T | 1.65943e-05 | 0.00288043 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133536 | CACATACTCCATTTA[C/T]AGTGCCATAAAGTTC | 25831 |
rs773224017 | snp | C/T | 1.72677e-05 | 0.00293829 | missense | HECTD1 | GRCh38.p7 | 14:31109569 | CGCTCCACAGTGGCT[C/T]CACGTCGGTTCTGTA | 25831 |
rs773226972 | snp | A/G | 1.6571e-05 | 0.0028784 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139935 | TCATACAAATGGAGA[A/G]GTAGACGTTCAATAG | 25831 |
rs773228543 | snp | A/T | 1.66352e-05 | 0.00288398 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169329 | TAACAGTAGATGGCT[A/T]CAAAAGAAAGAATGT | 25831 |
rs773261934 | snp | A/C | 3.31296e-05 | 0.00406985 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175005 | CCACAGAGTCTTGAT[A/C]CCACAGCCATAGCAG | 25831 |
rs773263594 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176783 | TCTACTAAAAATACA[A/G]AAAATTAGCCGCGCA | 25831 |
rs773272998 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130528 | GAAATTTTACAATCT[C/T]ATTTTAGTGTTATAA | 25831 |
rs773307266 | snp | A/C/G | 8.62454e-05 | 0.00656629 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106610 | CTTTAAAACTTATTC[A/C/G]TGCATTGGATTGAAG | 25831 |
rs773326938 | snp | A/G | 1.65608e-05 | 0.00287752 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129201 | GCTGCTACTGGCCAC[A/G]CTACACACAGAACTG | 25831 |
rs773331072 | snp | C/T | 1.86485e-05 | 0.00305351 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144112 | CTTGATAAACTTACA[C/T]TGTTTAACACAGTAA | 25831 |
rs773349079 | snp | C/T | 1.65638e-05 | 0.00287778 | missense | HECTD1 | GRCh38.p7 | 14:31109413 | TCAAGAACTGATTTC[C/T]GATCTGCATGTATTT | 25831 |
rs773349179 | snp | C/G | 1.65723e-05 | 0.00287852 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116397 | TGTTACTTTCAAAGT[C/G]AGAGCTAATCGAGGT | 25831 |
rs773362236 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117973 | CAAAGAACATTTATA[C/G]AACCGAGTATACTTA | 25831 |
rs773364080 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196453 | GAAGAAAACAGGTCA[A/G]TATAGAAAAGGCAGG | 25831 |
rs773369370 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116806 | TGGATAATTTTTGTA[C/T]TTTTAGTAGAGACGG | 25831 |
rs773392885 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188394 | GCGCCTGCCACCACA[A/C]CTGGCTAATTTTTGT | 25831 |
rs773405701 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174470 | CAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTCC | 25831 |
rs773411499 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165905 | GGCTGGAATGCAGTG[A/G]CGCAATCTTGGCTCA | 25831 |
rs773457775 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31111638 | GTTTTCACACAGCGC[A/G]CTTCTCTGGGTGGAA | 25831 |
rs773461546 | snp | C/G | 0.000558088 | 0.0166953 | intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31123570 | CGATGGAGACTGGGT[C/G]AAATTACATTGTCCT | 25831 |
rs773473206 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195251 | ATTAAAATACACATA[A/C]AAATTTGACTGCAAT | 25831 |
rs773483509 | snp | A/G | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100347 | TAGTATGGCATTTAG[A/G]AAATAAAAATATACT | 25831 |
rs773487302 | snp | G/T | 1.70839e-05 | 0.00292262 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112594 | AAGGCATTCATGCAT[G/T]CATGCATTCATTCAT | 25831 |
rs773508904 | in-del | -/A | 1.72021e-05 | 0.0029327 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133231 | AAGTGCTGAGCACCT[-/A]ACTCACCATTGTGTA | 25831 |
rs773524775 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191714 | ACTTAAGAAAACAGA[C/G]AAGGGCTGGCGTGGT | 25831 |
rs773540655 | snp | A/G | 1.65839e-05 | 0.00287953 | missense | HECTD1 | GRCh38.p7 | 14:31112465 | GCTGTCTAGTTTCAA[A/G]TGGTATTAGAAAAGG | 25831 |
rs773558286 | snp | A/T | 0.000102338 | 0.00715253 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141983 | AGTATAAAGTCCAAA[A/T]AAAAATAATTTAAGG | 25831 |
rs773575136 | snp | A/C | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099788 | CAACATTTAAAAATC[A/C]TTCTTGGATCTCACT | 25831 |
rs773588176 | snp | C/T | 4.98923e-05 | 0.00499436 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133395 | TCTAAGATTAGCTTC[C/T]GCTTCTTTAGCTGCT | 25831 |
rs773593381 | in-del | -/G | 2.69946e-05 | 0.00367377 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141969 | TAAAGAAAACAAAAA[-/G]TATAAAGTCCAAAAA | 25831 |
rs773601514 | snp | C/T | 3.31241e-05 | 0.00406952 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119804 | AGAAAACTGTCTCTT[C/T]AGCACATAATCATCA | 25831 |
rs773606166 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137897 | GTTTAAATAAACTTA[-/C]AAAACTTCTTAACTT | 25831 |
rs773624390 | snp | A/G | 1.66596e-05 | 0.00288609 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150246 | TAGAATTATTCAATT[A/G]AACATGGAAAATAAT | 25831 |
rs773702870 | in-del | -/TATC | 2.33828e-05 | 0.00341919 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109613 | TCTGAAATAGAAAAA[-/TATC]TATGAGCTGCAGCAT | 25831 |
rs773710295 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170727 | TTATTGAAAATGTTG[C/T]TGTAGTGTAAAGATG | 25831 |
rs773719196 | in-del | -/AAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200490 | GTCTCCATCTAATTT[-/AAA]AAAAAAAAAAAAAAA | 25831 |
rs773719452 | snp | C/T | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173304 | AGACTTTGGCAAAGC[C/T]TTTCGTCCTTCAAAT | 25831 |
rs773732035 | snp | C/G | 1.65605e-05 | 0.0028775 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129048 | TGCACTGGAAGATGA[C/G]CCTACTTCTGTTTGA | 25831 |
rs773743845 | in-del | -/AAAAACCCCC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187044 | AAAAAAAAAAAAAAA[-/AAAAACCCCC]AAAAAAAACACCCAA | 25831 |
rs773758173 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202652 | AAAGACCTTTCCAAA[C/T]CAATCACTTTATTCA | 25831 |
rs773771035 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157574 | TCTATATTCTACACT[C/T]TACTAGCATGAATGT | 25831 |
rs773784286 | snp | A/T | 1.67863e-05 | 0.00289704 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100897 | TCACTAGTATTTTTA[A/T]AGTCTCTGATGTCTC | 25831 |
rs773785017 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154129 | GTTAGACTCTCCTTG[-/T]TTTTTTTTTTTTTTG | 25831 |
rs773808944 | in-del | -/AC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203747 | TGTTTTAACATGGCA[-/AC]ACTTTTTTTTTTTAT | 25831 |
rs773875539 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163060 | CAGGGTAAGATCCTG[-/AC]ACACACACACACACA | 25831 |
rs773885372 | snp | A/G | 1.65921e-05 | 0.00288024 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31100945 | TCAATTGAGATGAAA[A/G]CCTTTCTCCATTGTA | 25831 |
rs773889326 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185263 | AGAATGGTGTGAACC[C/T]AGGAGGCGAAGCTTG | 25831 |
rs773909337 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142414 | AAGGGACTATGGGAC[-/T]TCATTGAAGTTCCAG | 25831 |
rs773943661 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137304 | CCCGGCTACTTTTTG[C/T]ATTTTTAGTAGAGAT | 25831 |
rs773954522 | snp | C/T | 1.67719e-05 | 0.0028958 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148716 | AGCACATCCAACAGA[C/T]ATACCTTTTGCTTTG | 25831 |
rs773956778 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115806 | AAAACACTTTATACA[C/T]GTTAATTCATTAATT | 25831 |
rs773969401 | in-del | -/TC | 1.67837e-05 | 0.00289682 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100900 | CTAGTATTTTTAAAG[-/TC]TCTGATGTCTCCCAT | 25831 |
rs773977522 | in-del | -/TATTAAAAGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174186 | TGAACAATAAAAAGT[-/TATTAAAAGC]CATTAAAAGCCAAGT | 25831 |
rs773982222 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129982 | ACTTCTTAAATGGAA[A/G]AACTGTTTAAGAAAT | 25831 |
rs773984183 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103770 | GGTGGGAGTTCGAGA[C/G]CAGCCTGACCAACAT | 25831 |
rs773986491 | snp | A/G | 0.000115924 | 0.00761239 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129069 | TTCTGTTTGAGGGAC[A/G]TTTTCAGCAGATGAA | 25831 |
rs773987188 | snp | A/G | 1.80416e-05 | 0.00300341 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178283 | AATCATATTACATCT[A/G]GGGTTATTAAATTCT | 25831 |
rs773998104 | snp | A/C/T | 3.31803e-05 | 0.00407299 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31113999 | GGTAGGTTATCAAGT[A/C/T]ATTCTTTGGTAATTC | 25831 |
rs774003496 | snp | C/T | 1.66258e-05 | 0.00288316 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123073 | AAACCCACAACCTTA[C/T]GTCAACACAATTAAG | 25831 |
rs774004940 | snp | A/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205857 | CATAGCTGTTCAAGG[A/G]CTATTAGTTGCATGT | 25831 |
rs774021525 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31149946 | GCAAAAATATGAGAA[A/T]AAAACCAAACTGTAG | 25831 |
rs774045428 | snp | C/T | 4.97376e-05 | 0.00498662 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136513 | GCTTATTTCACCGTG[C/T]CCTTGCCAGAAACTC | 25831 |
rs774046168 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116607 | TTAAGACTCTCTAGG[C/T]GTCGACATTTTTGCT | 25831 |
rs774047327 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128982 | ACTATCAGGGCCTAA[C/T]TTCCTTTCAGCATTT | 25831 |
rs774052729 | snp | A/G | 4.9802e-05 | 0.00498984 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133370 | GGGAACGTACTAGAC[A/G]TCTCTGCCGTCTAAG | 25831 |
rs774073259 | snp | C/T | 4.96857e-05 | 0.00498401 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168378 | TATGGGTGCCATTTC[C/T]GGATCTCCTTTGGGC | 25831 |
rs774078874 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148829 | AGAATATTCACAGAG[C/T]TTACTTTGTTACAAT | 25831 |
rs774108425 | snp | A/G | 1.72184e-05 | 0.00293409 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113862 | TCAAAATAGTGTTTT[A/G]ATGCCAATATATACC | 25831 |
rs774146491 | in-del | -/GAG | 0.000186133 | 0.0096453 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123635 | AAAAACTGAAAAAAA[-/GAG]GACTAAAGGGATTAT | 25831 |
rs774154597 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146917 | ATACTAAAAAACAAG[A/G]TGAAAAAATGTTGTC | 25831 |
rs774170054 | snp | A/G | 3.4293e-05 | 0.00414069 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135496 | ATTTGTTCCAATCCA[A/G]TAAATGATTCCATTT | 25831 |
rs774182222 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135745 | CTCATTTAGGCCGGG[C/T]GCGGTGGTTCACGCC | 25831 |
rs774225217 | snp | C/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31174924 | ACCTGATGATCTTCA[C/T]GCTTTAATAAACTAG | 25831 |
rs774230870 | snp | A/G | 1.84354e-05 | 0.00303601 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173756 | GTCAACACCACGACG[A/G]GTAAATCGGTCAGCC | 25831 |
rs774231157 | snp | A/T | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122962 | GTCATCTTCATTCTC[A/T]TCATCTTCTTCATCT | 25831 |
rs774246240 | in-del | -/GCA | 2.03357e-05 | 0.00318865 | cds-indel, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173787 | GTGATGCAAAGCATC[-/GCA]GCAGAGCTCCATCTG | 25831 |
rs774259906 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31164792 | TCTCCAAACATTTAA[A/G]ATGATAAAAGAAAAT | 25831 |
rs774276110 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31176461 | AGTTTCAGTATCTAA[C/T]ATGGTAAATAAATAG | 25831 |
rs774315458 | snp | G/T | 3.74476e-05 | 0.00432694 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157354 | TGAAGTTAAAATAAA[G/T]CAAAATGCATGCATT | 25831 |
rs774332788 | in-del | -/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132213 | GAGGCCGAGGTGGGT[-/G]GATCACCTGAGGTCG | 25831 |
rs774340442 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209732 | TAGGGAGACCCTGTC[C/T]CTACAAATAATTTTT | 25831 |
rs774353216 | snp | G/T | 1.65699e-05 | 0.00287831 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148970 | ACCAGGTAAATCTTC[G/T]TTCAATATTGTAGCT | 25831 |
rs774360106 | snp | C/T | 3.38467e-05 | 0.00411366 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133245 | CTACTCACCATTGTG[C/T]AGTTCTCCTGTGACA | 25831 |
rs774373915 | in-del | -/A | 2.45143e-05 | 0.00350094 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133688 | ACCTGTTAATATGTT[-/A]AGAGAAAAAATTATG | 25831 |
rs774377094 | snp | C/G | 1.66095e-05 | 0.00288175 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105354 | AAAGTGAAAGGAGAG[C/G]AATTATGCTAAAAAT | 25831 |
rs774400350 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132439 | CGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 25831 |
rs774403598 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141527 | GCCCAGGAGGTTGAG[A/G]CTGCAGTGAGCCAAG | 25831 |
rs774408551 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198374 | TTCAAAATTTAATCA[C/T]GTATGCCTTTCATTT | 25831 |
rs774423445 | snp | A/G | 1.80003e-05 | 0.00299997 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149144 | TTGTAACTTCTCTAA[A/G]AATTCACTTCGGCTT | 25831 |
rs774427673 | snp | A/G | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119300 | CTACCACAATCTAAA[A/G]TAGAGTTTTGTAAGG | 25831 |
rs774428633 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130666 | ACACACCCATCCACA[C/T]ACCCAGATGCTCACC | 25831 |
rs774451100 | snp | C/T | 3.33918e-05 | 0.00408592 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134881 | ACTAACCCTGGTTCA[C/T]TGAGACTGCAGTCAT | 25831 |
rs774547730 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154259 | TCTCACCCTCCCAAG[C/T]AGCTGGGATTACAGG | 25831 |
rs774548815 | snp | C/T | 6.62712e-05 | 0.00575597 | missense | HECTD1 | GRCh38.p7 | 14:31116281 | TTATCTGATTTCACA[C/T]TGCCATTACAGGACA | 25831 |
rs774622097 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192735 | AATCTCAGCACTTTG[G/T]GAGGCCAAGGCAGGC | 25831 |
rs774637385 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145104 | AGTTATTTGAGGAAA[C/T]AACCTATGTATGTTC | 25831 |
rs774649788 | snp | A/G | 3.31257e-05 | 0.00406962 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127906 | TGTTGCTGTAGCTAC[A/G]TTGCTGCTGCTAGTA | 25831 |
rs774669306 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179875 | TACCTTTAGTAGCCT[G/T]TAAGAAATATCTGTA | 25831 |
rs774670756 | snp | A/C | 4.12363e-05 | 0.00454053 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113068 | GAAAAGTCCAACAGT[A/C]ATAGAATGAAGAGTT | 25831 |
rs774683814 | snp | A/C | 1.68946e-05 | 0.00290638 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169514 | AACAATACTTTATTT[A/C]TTTGACATCCAACTA | 25831 |
rs774698407 | snp | A/G | 2.32501e-05 | 0.00340948 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144302 | ATCAAAAACATAAAC[A/G]TAGCTCTTAAAATAA | 25831 |
rs774703677 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110814 | TTTGTGTTTTTTTGT[A/G]GAGATGGGGTTTTGC | 25831 |
rs774725588 | snp | C/T | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100497 | CATTAATTCTCTATG[C/T]TTTAAGGAAGCAGGA | 25831 |
rs774745835 | snp | A/G | 1.7423e-05 | 0.00295147 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113229 | ATAAAAATATAAACT[A/G]ACTTGCTTTAAAACT | 25831 |
rs774747453 | snp | C/T | 1.7969e-05 | 0.00299736 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144132 | TAACACAGTAAGAAG[C/T]GCTTGTACCAAGCCA | 25831 |
rs774797604 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124633 | TCCAAAAGGAGTGCA[A/G]GAGTGGGCAAGGGCT | 25831 |
rs774801075 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31150563 | CTATAACTAAATCTT[-/A]ACAAATAAGTGTTAA | 25831 |
rs774868221 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160295 | ATGATACATAATACT[C/T]ACAACATAAAATTTT | 25831 |
rs774872203 | snp | C/T | 1.691e-05 | 0.0029077 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156858 | TTCTGGTTTTGATTC[C/T]TCTTCATTCTCATCA | 25831 |
rs774899228 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171561 | AGTACAGGATATGCA[C/T]ACAGATATAAAAAAG | 25831 |
rs774908276 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31199765 | GTTTCATTCTGAATA[C/T]GGCAAATAGCAGTAA | 25831 |
rs774922910 | snp | A/G | 1.65685e-05 | 0.00287819 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175028 | CATAGCAGAGTGCAA[A/G]GTGTCTTTATGAACT | 25831 |
rs774924298 | in-del | -/C | 1.65682e-05 | 0.00287817 | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119855 | TCCTTTAGTTTCGTA[-/C]TCTTCTTCTTCCTAT | 25831 |
rs774980567 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204207 | GACACAATAAACATA[C/T]GTGTGCATGTGTCTT | 25831 |
rs775001546 | snp | A/G | 1.80231e-05 | 0.00300187 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144194 | TTTCATCCTTCAAAA[A/G]TACAATTAGGTTTTC | 25831 |
rs775006109 | in-del | -/A | 1.65682e-05 | 0.00287817 | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31174967 | CACAAATTTCTAAAG[-/A]AGAATCTTGAGGCTC | 25831 |
rs775013458 | snp | A/T | 1.66023e-05 | 0.00288113 | missense | HECTD1 | GRCh38.p7 | 14:31101294 | AGAAGACATGCCACA[A/T]AAAACCCTCACAAAC | 25831 |
rs775028873 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138662 | ATCAGGTGCAACTAC[C/T]GCACTGTAAAACTCC | 25831 |
rs775080321 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112074 | TTTAGCCACGGTAAC[A/C]CTTGTGGGGCATTCC | 25831 |
rs775097911 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104607 | ATATACTTTGTTCCC[A/G]TCATGATTCTTTCAT | 25831 |
rs775103774 | snp | A/G | 1.65614e-05 | 0.00287757 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129206 | TACTGGCCACGCTAC[A/G]CACAGAACTGCTGCT | 25831 |
rs775128225 | snp | C/T | 1.65949e-05 | 0.00288048 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156897 | AGGACCTGCCAACGT[C/T]GACACTTTGCTAATT | 25831 |
rs775149634 | snp | C/T | 1.67307e-05 | 0.00289224 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173468 | TTTAATATATTAGCA[C/T]TATACAAAAACACTT | 25831 |
rs775180612 | snp | A/T | 1.6563e-05 | 0.00287771 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119837 | CCATGTTCTCCGGCG[A/T]CCTCCTTTAGTTTCG | 25831 |
rs775191711 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155976 | TCTCAGGCCGGGTGC[A/G]GTGGCTCACGCCTGT | 25831 |
rs775193399 | snp | C/T | 1.6641e-05 | 0.00288448 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107558 | TCACAAAATGAGAAA[C/T]ATTCTTACGTGACGA | 25831 |
rs775227058 | snp | G/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209854 | TGCAGTGAGCCATGA[G/T]CATGCCACTGCACTA | 25831 |
rs775239237 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177663 | GGTGATTGTTACTAT[C/T]ATAATACAAAATGAT | 25831 |
rs775239854 | snp | G/T | 1.65636e-05 | 0.00287776 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173369 | TATCAAGCACACATC[G/T]TTCATCACCCTGCAA | 25831 |
rs775243717 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186841 | CCAGCCTGGCCAACA[C/T]GCGAAACCCCGTCTC | 25831 |
rs775280747 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171532 | ACACTAGGTGACTAG[C/T]TGAATAAACTTGTAG | 25831 |
rs775297193 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171700 | TTTTATTGAATCTGT[A/G]TTAGGAAACACTAAA | 25831 |
rs775326410 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152244 | CAAACAGCCAGAGTA[C/G]AAAATCCTCATAGAT | 25831 |
rs775410545 | snp | A/G | 1.6563e-05 | 0.00287771 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150201 | TTGCAATTCTTTAGC[A/G]TCTTCCTGTGGTTCA | 25831 |
rs775411264 | snp | C/T | 3.53001e-05 | 0.00420105 | missense | HECTD1 | GRCh38.p7 | 14:31109575 | ACAGTGGCTTCACGT[C/T]GGTTCTGTAACCATA | 25831 |
rs775414415 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165752 | TGCCTTTGTAGGAAT[A/G]TAGCAGTACATAAGA | 25831 |
rs775440932 | snp | C/T | 1.66056e-05 | 0.00288141 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148733 | TACCTTTTGCTTTGT[C/T]TTTTCTAACTTAGAT | 25831 |
rs775461833 | snp | A/G | 1.6693e-05 | 0.00288898 | missense, intron-variant | HECTD1 | GRCh38.p7 | 14:31114046 | TGCTCCACATGCTCT[A/G]TAGACCAGCAACCCT | 25831 |
rs775489494 | snp | C/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205867 | CAAGGGCTATTAGTT[C/G]CATGTCCCTTTCATC | 25831 |
rs775508911 | snp | A/C | 1.67055e-05 | 0.00289006 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123093 | ACACAATTAAGAAAG[A/C]ATAACAAAGGAACTT | 25831 |
rs775510691 | in-del | -/AA | 2.69291e-05 | 0.00366931 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149198 | CAAAATCTTATTTCT[-/AA]TTCAAGTATGACATG | 25831 |
rs775524626 | snp | C/G/T | 3.34064e-05 | 0.00408684 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173660 | TTTGCATGCTGATGA[C/G/T]GGTCCTGAAACAGTA | 25831 |
rs775535200 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188652 | TTTTATTTCTTCTTA[G/T]CCATTGTAACTCTCT | 25831 |
rs775553943 | snp | C/T | 3.31587e-05 | 0.00407164 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105554 | GCTAAGAGGATATGT[C/T]AGAACTTACAACTAT | 25831 |
rs775556300 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124069 | AAAATGGTGTGTCTT[A/T]ACACTCAACAGCATC | 25831 |
rs775592629 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195471 | GATAAAAATCTATCT[C/G]TGATAAATTTTCCTT | 25831 |
rs775602378 | in-del | -/A | 0.000232219 | 0.0107729 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144264 | TCAATACACTAAAAG[-/A]AAAAAAAAATTTAAT | 25831 |
rs775609648 | snp | C/G | 3.36564e-05 | 0.00410208 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31172121 | AAAATTTACTTCAAA[C/G]GCTGAAATTTTGAAG | 25831 |
rs775613817 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31107871 | TGTTATTTTAATTTT[C/T]CTAAAGAGTCCACTT | 25831 |
rs775635926 | snp | C/T | 3.5033e-05 | 0.00418513 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141846 | CAAATTCAAAGAAAT[C/T]TGAGATTTTACCTTT | 25831 |
rs775664440 | in-del | -/GT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122264 | TTCATACACACACAC[-/GT]GTGTGTGTGTGTGTG | 25831 |
rs775674085 | snp | A/G | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119833 | CATCCCATGTTCTCC[A/G]GCGTCCTCCTTTAGT | 25831 |
rs775702548 | snp | A/G | 1.6574e-05 | 0.00287867 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128755 | CTAGATGTTTCTCTT[A/G]AGGACAGGTTAGGTA | 25831 |
rs775740718 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137457 | TTTAGGCCAGGCACA[A/G]TGACTCAGACCTGTA | 25831 |
rs775765596 | in-del | -/GTGTGCGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134564 | TGTGTGTGTGTGTGT[-/GTGTGCGC]GCGTATGTATATACA | 25831 |
rs775795293 | snp | A/G | 1.65655e-05 | 0.00287793 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116306 | AGGACAATTGAAGCA[A/G]TTTTTGTACATAGTA | 25831 |
rs775810072 | snp | A/C | 1.75665e-05 | 0.0029636 | intron-variant | HECTD1 | GRCh38.p7 | 14:31175164 | AAAACAAATGTAACG[A/C]AAGAATGCAAGCCTG | 25831 |
rs775817128 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193843 | GCAGAAGAATCGGTT[A/G]AACCCGGGAGGTGGA | 25831 |
rs775827092 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135073 | TCATTGCTATGACAA[C/T]TTAAAGCTGAATTAT | 25831 |
rs775842556 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145234 | CCAGCATAACTCTAA[C/T]GCAACAGAAAAAAAC | 25831 |
rs775861622 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155574 | AACATGACACAAAGT[G/T]AGGCTCTTTGTTCAA | 25831 |
rs775885803 | snp | A/G | 1.71135e-05 | 0.00292514 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144778 | ACTAAAATTCACTAC[A/G]TATCATTAAAATCTA | 25831 |
rs775890190 | snp | C/T | 2.23072e-05 | 0.00333963 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149175 | TCTATAAAGACAAAA[C/T]ACTTGTTTCAAAATC | 25831 |
rs775893145 | snp | G/T | 1.65853e-05 | 0.00287964 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31106768 | AATTTGGCGCCTCTT[G/T]ATAGCAAGGTCTTTA | 25831 |
rs775924105 | snp | C/G | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178047 | TTCGGCTAAGTCTCT[C/G]CTAGTCCTGTTGTTA | 25831 |
rs775936710 | snp | A/C | 1.70142e-05 | 0.00291664 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144921 | ATGGTCATCGTATAA[A/C]TCTCGAGCCATAGTT | 25831 |
rs775941480 | snp | A/C | 1.67638e-05 | 0.0028951 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171986 | TAACGAATCATAAAG[A/C]TGCTTTTTATTAATA | 25831 |
rs776009592 | in-del | -/CACATGCG | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163098 | ACACACACACACGCA[-/CACATGCG]CACACACACACACGG | 25831 |
rs776011123 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130810 | AATCTACATAAGTAG[C/T]TTAGATGAGATTTTT | 25831 |
rs776023055 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112870 | CCACCTTGGCCCCCA[A/G]AATGCTGGAATTACA | 25831 |
rs776065989 | snp | A/G | 8.63322e-05 | 0.00656952 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171820 | TAATTTTTAAACCAT[A/G]TAAATGTTAAAAATT | 25831 |
rs776084214 | in-del | -/AA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132438 | GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 25831 |
rs776094793 | snp | A/G | 1.65627e-05 | 0.00287769 | missense | HECTD1 | GRCh38.p7 | 14:31113384 | CCATTGCCTGCTTTG[A/G]CCTGAGGTTGTTCTT | 25831 |
rs776099837 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146194 | AGTATTCATTAAAAT[G/T]TGTAACCTCAAAATC | 25831 |
rs776135676 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112958 | TATAAACCTGTAATT[A/T]GGAAATAAATGCAAA | 25831 |
rs776138734 | snp | C/T | 4.96981e-05 | 0.00498463 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31134935 | CAGTTCTGTCCATCT[C/T]TGGATACCTGGAAAA | 25831 |
rs776145882 | snp | A/T | 1.68843e-05 | 0.00290549 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113240 | AACTGACTTGCTTTA[A/T]AACTGCTATAGAAAT | 25831 |
rs776147746 | snp | C/G | 1.6577e-05 | 0.00287893 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121462 | TGATGCGTTACATCA[C/G]AGCGGGAGCCAGCTC | 25831 |
rs776148529 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153495 | ATTACAGGCATGAGG[C/T]ATCATGCCCAGCCGA | 25831 |
rs776187015 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101682 | CTGTAATCCCAGCTA[C/T]TTGGGAGGCTAAGGC | 25831 |
rs776204796 | snp | A/G | 3.34538e-05 | 0.00408971 | missense | HECTD1 | GRCh38.p7 | 14:31101323 | ACCTCAGGAAACCAG[A/G]GCTAAAAGAACAAAA | 25831 |
rs776255936 | snp | C/T | 1.65707e-05 | 0.00287838 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109393 | TAATTTTATATGAGA[C/T]TACCTCAAGAACTGA | 25831 |
rs776285886 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205522 | TATTTTGAAAATGAA[A/C]CAACCAAGCTATGGG | 25831 |
rs776292201 | in-del | -/AAGC | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163122 | ACACACACACACGGA[-/AAGC]AAGAAAAGAAAACCA | 25831 |
rs776310462 | snp | A/G | 1.658e-05 | 0.00287919 | stop-gained, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121478 | AGCGGGAGCCAGCTC[A/G]ACGTTGCAGGGATGG | 25831 |
rs776311807 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124959 | ACTACAGGGATCCGC[C/G]ACCACACCCGGTTAG | 25831 |
rs776312322 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31109899 | GCCCCAACATCATTC[-/A]AAAAAAAGGAAAAAT | 25831 |
rs776312694 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125618 | CCTTATGCAATGAAT[G/T]TATAACACTTTGGTG | 25831 |
rs776319921 | in-del | -/CT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116598 | GTCAGCTACTTAAGA[-/CT]CTCTAGGCGTCGACA | 25831 |
rs776338089 | snp | C/T | 4.97335e-05 | 0.00498641 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157275 | AGCAAAAATGAATCA[C/T]TTTTCGAATTAGAGC | 25831 |
rs776340780 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181324 | TAGTTAAAGAGCCAG[A/T]TTAGGCTGGGTGCAG | 25831 |
rs776342723 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124779 | TCTAAAATAAAAATT[A/G]TATTAATTTTTTTCA | 25831 |
rs776350200 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31138934 | ATAAAGTTCTGGGCT[A/G]GGACATTAGTAAAAT | 25831 |
rs776378066 | snp | A/G | 1.66718e-05 | 0.00288715 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173563 | TGCAAAGTGTTGAGA[A/G]CAGACTTACAATTGT | 25831 |
rs776378448 | snp | C/T | 1.65726e-05 | 0.00287855 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101159 | TTCATTTGGATTCCC[C/T]ATTAGCCAGAGAGCT | 25831 |
rs776390254 | snp | A/G | 1.66454e-05 | 0.00288486 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157124 | TTCAGACTACTAGCT[A/G]AAGGAAATTAATGCT | 25831 |
rs776403711 | snp | A/T | 1.65745e-05 | 0.00287871 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31139909 | GGAGGTTATATGTGG[A/T]TCCTGGTGTATCATA | 25831 |
rs776429541 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161737 | AGCCCAGCCAACATG[A/G]CAAAACCCCATTTTT | 25831 |
rs776455019 | snp | C/T | 0.000116033 | 0.00761598 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136686 | CAAAAACGATCAAAA[C/T]ACTCTGGAAAACGTC | 25831 |
rs776471220 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116491 | GGGTGAAAAACAATT[A/G]TACTAAAACAAGCAG | 25831 |
rs776512044 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206621 | TATTCTTAAAAGTTA[-/AAA]AAAAAATAAAAAAAT | 25831 |
rs776544690 | snp | A/C | 3.31658e-05 | 0.00407208 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105376 | GCTAAAAATCCTTTA[A/C]AATTACCTCTAAAGG | 25831 |
rs776548017 | snp | A/G | 1.67621e-05 | 0.00289495 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173500 | TTCTGAAGATTAAAA[A/G]GCAAAGATTCAAAAA | 25831 |
rs776573474 | snp | C/T | 1.90976e-05 | 0.00309006 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173771 | GGTAAATCGGTCAGC[C/T]AGTGATGCAAAGCAT | 25831 |
rs776578807 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154069 | GTATATCCTTCTACG[C/T]TGCTCCTTTTCCAGG | 25831 |
rs776580004 | snp | A/C/T | 3.32255e-05 | 0.00407576 | missense | HECTD1 | GRCh38.p7 | 14:31107571 | AATATTCTTACGTGA[A/C/T]GAGATTCATCATCTG | 25831 |
rs776581105 | snp | C/G | 1.65737e-05 | 0.00287864 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148951 | TATTAGATTCAAATA[C/G]AAAACCAGGTAAATC | 25831 |
rs776626980 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104798 | CCACTTCAGCCTTGC[A/C]GGTAGCTGGGACCAC | 25831 |
rs776639674 | snp | A/G | 1.65633e-05 | 0.00287774 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173388 | ATCACCCTGCAATGC[A/G]CTTTCAATTGAATCT | 25831 |
rs776658432 | snp | C/G | | | missense | HECTD1 | GRCh38.p7 | 14:31116260 | GGCTCCCAAATACGC[C/G]TAAGTTTATCTGATT | 25831 |
rs776671501 | snp | C/G | 1.65828e-05 | 0.00287943 | missense | HECTD1 | GRCh38.p7 | 14:31112458 | AAATAAAGCTGTCTA[C/G]TTTCAAATGGTATTA | 25831 |
rs776686359 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126803 | CCCTCTCACCTCAGC[C/T]TTCTCAGTAGCATGA | 25831 |
rs776699987 | snp | C/T | | | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157240 | ATCAGAATCACAAAC[C/T]TCTTTTAACAGTGCT | 25831 |
rs776710862 | snp | A/G | 0.000221833 | 0.0105293 | missense | HECTD1 | GRCh38.p7 | 14:31114335 | TTCATTTCTCTGTAC[A/G]TGATTCTAAACATGA | 25831 |
rs776733773 | snp | C/T | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31099692 | GGTAATAACTGGAAT[C/T]TGGAAAATCTACTTT | 25831 |
rs776747029 | snp | C/T | 1.6696e-05 | 0.00288924 | intron-variant | HECTD1 | GRCh38.p7 | 14:31150229 | TCATCTTCCTAAATG[C/T]GTAGAATTATTCAAT | 25831 |
rs776754195 | snp | A/C | 1.65822e-05 | 0.00287938 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31174946 | ATAAACTAGACAGAG[A/C]TTCTACACAAATTTC | 25831 |
rs776758396 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31190368 | ATAAATGATCCACAA[A/G]TATTGTGGTGCGGCT | 25831 |
rs776762047 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105942 | CTGGCTTTGCAAAGA[C/T]TGCATGAAACCACCT | 25831 |
rs776796561 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31127477 | CTGCCTCAGCCTCCT[C/G]AGTAGCTGGGATTAC | 25831 |
rs776797217 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208805 | CTATGGTCCCAGCTA[C/T]TGGAGCGGTTGAGAT | 25831 |
rs776820002 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122366 | CACTGGCTAAGTTCG[C/T]GTGTGTGCGCGCATG | 25831 |
rs776830136 | in-del | -/A | 4.99979e-05 | 0.00499965 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173446 | AAAGAGAATGGGAAG[-/A]AAGATGTTTAATATA | 25831 |
rs776830578 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31109006 | AGCACAATTCAAGTG[A/T]AACAATATTACAAAA | 25831 |
rs776847310 | snp | A/C | 3.33946e-05 | 0.00408609 | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119660 | CCCTACTTTTCATAT[A/C]TGATTTAGTATGTAT | 25831 |
rs776869991 | in-del | -/GT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124060 | AACAGAAAAAAAATG[-/GT]GTGTCTTAACACTCA | 25831 |
rs776889308 | in-del | -/TA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193431 | ACAGTACTATTTGTC[-/TA]TGTTTATATCAATAC | 25831 |
rs776895450 | snp | A/G | 2.56888e-05 | 0.00358381 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141962 | CATGCTCTAAAGAAA[A/G]CAAAAAGTATAAAGT | 25831 |
rs776902336 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120922 | AGTGGCTCATGCCAA[A/G]GCAGGCAGATTGCTT | 25831 |
rs776920285 | snp | A/G | 2.23556e-05 | 0.00334325 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109604 | TACTATTGCTCTGAA[A/G]TAGAAAAATATCTAT | 25831 |
rs776923043 | snp | G/T | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31121262 | TCTTTGTGTAACTGT[G/T]TGGTAGCTCCCTCCT | 25831 |
rs776929765 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31169889 | AACTCCATCTCAAAA[A/G]ACAATACAAAGCAGC | 25831 |
rs776945228 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31207757 | GAGGGAGAGCCAGGC[A/G]GGGAAGCTGCCGAGG | 25831 |
rs776970016 | snp | A/G | 1.66054e-05 | 0.00288139 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31116427 | TGACGGAGTACATTC[A/G]ACTTCTTCCAAGAGC | 25831 |
rs776972678 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132790 | AACACTTTGAAATAA[C/T]AATAATCTACTAACA | 25831 |
rs776976770 | snp | C/T | 1.68009e-05 | 0.00289831 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171994 | CATAAAGCTGCTTTT[C/T]ATTAATATTTCTATC | 25831 |
rs777014323 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181854 | ATACGTAAAATGCAC[-/T]TTTTTTTTATATCAA | 25831 |
rs777023454 | snp | C/T | 1.65619e-05 | 0.00287762 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135101 | TATCACGACTTAGTA[C/T]GTCTTCTAAGCGGCC | 25831 |
rs777024006 | snp | C/T | 3.30038e-05 | 0.00406212 | intron-variant | HECTD1 | GRCh38.p7 | 14:31141853 | AAAGAAATTTGAGAT[C/T]TTACCTTTCATCATC | 25831 |
rs777060935 | in-del | -/ATA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31128193 | TTATAGCACTATTAT[-/ATA]ATAATTACTTTGACC | 25831 |
rs777068742 | snp | A/G | 3.50766e-05 | 0.00418773 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113833 | TGCAAAACAAAGCAC[A/G]AAGCCATTTGCAATC | 25831 |
rs777080548 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31181866 | GCACTTTTTTTTATA[C/T]CAAGGTTTCAAGGAA | 25831 |
rs777099676 | in-del | -/T | 6.64033e-05 | 0.0057617 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119911 | TAATAAGATGCAAAA[-/T]TTCATTGTTGCAAAA | 25831 |
rs777124682 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155707 | GAATATGATAAGCAA[C/T]GTAATGTGTGCTCCT | 25831 |
rs777133555 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183835 | AAATCAGCCTCCCAA[A/G]TAGCTGGGACCACAG | 25831 |
rs777153814 | snp | G/T | 3.32419e-05 | 0.00407675 | intron-variant | HECTD1 | GRCh38.p7 | 14:31119918 | ATGCAAAATTTCATT[G/T]TTGCAAAAGCAATGT | 25831 |
rs777154958 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200698 | AGGCAGGAGAATCAC[G/T]TGAACCTGGGAGGTG | 25831 |
rs777210477 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31168674 | TAACAAATTAAGAAG[A/G]TAATTTTGGATACTC | 25831 |
rs777216709 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134143 | TTAAATAACGTATTA[A/G]TATTTTGTCTTTAAA | 25831 |
rs777224874 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110720 | TGCAATCTCAGCTCA[C/T]TGCAACCTCTGCCTC | 25831 |
rs777224916 | in-del | -/TTTC | | | downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31100007 | CTATAGAAAAACACA[-/TTTC]TTTATGTAGTAATTT | 25831 |
rs777233856 | snp | C/T | 1.66685e-05 | 0.00288686 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127789 | TTACAACTTACCATA[C/T]AAGGAATATTCTGCT | 25831 |
rs777266538 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117225 | CAAAAATGCAAAAAT[C/T]AGCTGGACATGATGA | 25831 |
rs777266585 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167697 | TGGATGGATTCATAC[C/T]TTCATGCATTTGCAC | 25831 |
rs777289408 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142559 | CGCCTCAGAATTACA[A/G]AAGAGTAGGTGGGAC | 25831 |
rs777291952 | in-del | -/GAG | 3.31241e-05 | 0.00406952 | cds-indel, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129235 | CTTCCTTTTCTACTT[-/GAG]GAGCCTGCAGCAGCA | 25831 |
rs777335128 | snp | A/T | 3.31279e-05 | 0.00406975 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169446 | TCTCTCAGATCTGGA[A/T]TTGCACCATGCCGTA | 25831 |
rs777339317 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104216 | CATAGAAATGATAAA[C/T]GTCCAAGATGATGGA | 25831 |
rs777346880 | snp | C/G | 6.6443e-05 | 0.00576343 | missense | HECTD1 | GRCh38.p7 | 14:31106805 | TTTAAAAATCTGGCT[C/G]TGTGTGGGTTTACTA | 25831 |
rs777354337 | snp | A/C | 0.000132765 | 0.00814645 | intron-variant | HECTD1 | GRCh38.p7 | 14:31123057 | GGAAATCTTGAAAAC[A/C]AAACCCACAACCTTA | 25831 |
rs777358156 | snp | A/G | 1.67332e-05 | 0.00289246 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133464 | TCACTTTTTACAAAA[A/G]TAATTGTTTTAGTAA | 25831 |
rs777362769 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187001 | GCACTCCAGCCTAGG[C/T]GAAAGAGCGAGAGAG | 25831 |
rs777407786 | snp | C/G | 1.65836e-05 | 0.0028795 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133352 | CCATGTATTTCAGAA[C/G]CTGGGAACGTACTAG | 25831 |
rs777410916 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209617 | TAACTTAAAAATTTC[C/T]GTCCAGGCTCCATGG | 25831 |
rs777417246 | snp | A/G | 1.65773e-05 | 0.00287895 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148814 | TTGGGGGGAAAAAAA[A/G]GAATATTCACAGAGC | 25831 |
rs777495767 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31129954 | ATGTGAGCCACTGCA[-/C]CCTGGCTTGGTTACT | 25831 |
rs777521391 | in-del | -/TG | 1.72537e-05 | 0.0029371 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113860 | ATCAAAATAGTGTTT[-/TG]TGATGCCAATATATA | 25831 |
rs777542814 | snp | C/G | 1.66228e-05 | 0.0028829 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105334 | ACCATAATTTCAACT[C/G]TCTCAAAGTGAAAGG | 25831 |
rs777564627 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31120646 | GTTGCTTTAAATTAC[C/T]ATGAGGCAGACAGCA | 25831 |
rs777575171 | snp | C/T | 4.96948e-05 | 0.00498447 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128915 | CATCAGGAGAACTAA[C/T]ACTGACAATTCCCAT | 25831 |
rs777593934 | snp | A/G | 1.65671e-05 | 0.00287807 | missense, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119733 | GGTATTTCTAGATCA[A/G]TTGTCTGCTGGACAT | 25831 |
rs777595239 | snp | C/T | 4.9703e-05 | 0.00498488 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150021 | GTCAGATCCACCTTC[C/T]GGACTACCACTTGAA | 25831 |
rs777610158 | snp | A/T | 1.76627e-05 | 0.00297171 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173738 | CTTGGCTAATGGAGC[A/T]GGGTCAACACCACGA | 25831 |
rs777610994 | in-del | -/CAACT | 0.000100095 | 0.00707372 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107534 | TTGAAAGCAGAGTCA[-/CAACT]CAAGTCACAAAATGA | 25831 |
rs777613179 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189987 | CAAGATGATACAGCT[C/T]CTGCTGCATTCTTTT | 25831 |
rs777627047 | snp | C/T | 1.66424e-05 | 0.0028846 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31112532 | AGCCCCACTTGCCAG[C/T]GCCAATGGTTCCTGC | 25831 |
rs777635083 | snp | A/G | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100120 | GACACAGTTCTGTAC[A/G]CTGCAAACATTTTAA | 25831 |
rs777648147 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200379 | GGCCAGGCACGGTGG[C/G]TCACGCCTGTAATCC | 25831 |
rs777662045 | in-del | -/TC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136198 | GTACAAAAACATTTT[-/TC]TGTTATCATTAGTCT | 25831 |
rs777667212 | snp | C/G | 1.65647e-05 | 0.00287786 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150206 | ATTCTTTAGCATCTT[C/G]CTGTGGTTCATCTTC | 25831 |
rs777670003 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31109879 | AAATAATAATCTGTT[G/T]TCCAAGCCCCAACAT | 25831 |
rs777672160 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153356 | GAGATCACGACAGAG[C/T]GAGACTCCATCTCAA | 25831 |
rs777672876 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31113832 | CTGCAAAACAAAGCA[C/T]GAAGCCATTTGCAAT | 25831 |
rs777701778 | snp | A/C | 1.67562e-05 | 0.00289444 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144886 | ACTACTCCACGAGGC[A/C]TGCTTTCAACAGCTT | 25831 |
rs777705318 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201480 | AATACAAAATGCTCA[G/T]TAGCTAATAACTCAT | 25831 |
rs777760235 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177143 | CTTCAAGTCTTGACT[A/C]TTCTGCTCACTACTC | 25831 |
rs777787245 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31101399 | CCACTATTTTCTAAG[G/T]CAGCAACAAGCCCCC | 25831 |
rs777808512 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122137 | CTGGGTAAGTTCATA[C/T]ACTGTGTGTGTGCTT | 25831 |
rs777821432 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31169647 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGGTCAC | 25831 |
rs777840149 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102265 | TTTGACAAAATCCTC[C/T]AAACTGTATATATGA | 25831 |
rs777871485 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206107 | TAAGTACGTTTGGAC[C/G]TAAGAGTGCTTAATG | 25831 |
rs777897508 | snp | C/G | 5.24104e-05 | 0.00511884 | intron-variant | HECTD1 | GRCh38.p7 | 14:31134857 | TTTCCAATTTGCAAA[C/G]ACTCCTCAACTAACC | 25831 |
rs777902865 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108733 | CTGTATATAAAGTGA[A/C]AGATGTAAAGCCTTG | 25831 |
rs777903222 | snp | A/G | 0.00041363 | 0.0143751 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173144 | TTTATATTTAAAAAA[A/G]TATTTTCTGACCTCC | 25831 |
rs777914032 | snp | A/C | 2.33626e-05 | 0.00341771 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113207 | ATAAAATTAATTAAT[A/C]AAATTAATAAAAATA | 25831 |
rs777938859 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31172534 | CCAGGAGGCAGAGGA[C/T]GCAGTGAGCCAAGAT | 25831 |
rs777979962 | snp | A/G | 3.31203e-05 | 0.00406928 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129169 | CGTTCCGTTTTGGTC[A/G]AACCCAAGCTGATGT | 25831 |
rs777986931 | snp | A/G | 1.68148e-05 | 0.0028995 | intron-variant | HECTD1 | GRCh38.p7 | 14:31178007 | AAGTAATGAGCCAAT[A/G]AGTAATACTTACCTT | 25831 |
rs777993395 | snp | C/T | 3.3162e-05 | 0.00407184 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121434 | TACCTGTGGTAGCTG[C/T]GAGGTAACAGCATGA | 25831 |
rs777993834 | snp | C/T | 1.68052e-05 | 0.00289867 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157006 | AAGTGGCCATCATCA[C/T]CATCCTGAAAAATAA | 25831 |
rs778043747 | snp | A/G | 1.81979e-05 | 0.00301639 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156822 | CTTCCTGATACCTCT[A/G]TAATTAAGACCACTC | 25831 |
rs778046729 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124361 | CATAGAATAAAATGT[C/T]TCTTCAAAACACAAC | 25831 |
rs778057477 | in-del | -/GAG | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209080 | AAACAAGAGGAAAAA[-/GAG]GATTCAACTATTTTG | 25831 |
rs778069681 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193448 | TGTTTATATCAATAC[C/T]ACATTGTCTTTATTA | 25831 |
rs778069732 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179270 | CTAAAAATACAAAAA[C/T]TAGCTGGGCATGGTG | 25831 |
rs778079113 | snp | C/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144838 | AGTTCCCAAGATGAC[C/T]CTAACTGAGTTGCTA | 25831 |
rs778105100 | snp | A/G | 1.66424e-05 | 0.0028846 | intron-variant | HECTD1 | GRCh38.p7 | 14:31173436 | AAGATCCTAGAAAGA[A/G]AATGGGAAGAAAGAT | 25831 |
rs778123501 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173292 | AGATCCAGCACTAGA[C/T]TTTGGCAAAGCTTTT | 25831 |
rs778124249 | snp | A/G | 6.62405e-05 | 0.00575464 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129301 | CTGCTCCATGATTGC[A/G]TTGTGCCTGAAACAG | 25831 |
rs778164813 | in-del | -/A | 4.97991e-05 | 0.0049897 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148806 | CTGAACCTTGGGGGG[-/A]AAAAAAAAGAATATT | 25831 |
rs778197528 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105290 | ACAGGTGTGAGCCAC[C/T]GTGCCCAGCCGACCA | 25831 |
rs778202669 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103900 | TGAACCCAGGAGGTG[C/G]AGGTTGCAGTGAGCC | 25831 |
rs778219148 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152050 | AAGTTTGAGGCAACT[A/G]GAATATGTGGAGGCT | 25831 |
rs778221070 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31193248 | GGGTTTTTAAAAATA[A/T]ATATAGTGTGAGATA | 25831 |
rs778237803 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141634 | AGTAAACTAAGTGAT[-/A]CAGCTGCATTCATAC | 25831 |
rs778259392 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187461 | ACATCTACATAAGAG[A/C]TATGTCCAGCACTGG | 25831 |
rs778271579 | in-del | -/ATG | 1.67038e-05 | 0.00288992 | intron-variant | HECTD1 | GRCh38.p7 | 14:31171967 | AATTCTACCTGTAAA[-/ATG]ATAACGAATCATAAA | 25831 |
rs778273721 | snp | A/G | 1.66944e-05 | 0.0028891 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107525 | TTAACACTTTTGAAA[A/G]CAGAGTCACAACTCA | 25831 |
rs778300823 | snp | C/G | 1.65655e-05 | 0.00287793 | intron-variant | HECTD1 | GRCh38.p7 | 14:31101074 | AGCATCAACCTACAA[C/G]AAGAAAGCAAACACA | 25831 |
rs778304167 | snp | A/T | 1.67595e-05 | 0.00289473 | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31205976 | AAATTTGAAAAGTAA[A/T]GGGAGAAAAGTCCTT | 25831 |
rs778330169 | snp | C/T | 3.31895e-05 | 0.00407353 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148894 | ACATATCTACATACT[C/T]ACCCAGGGAAGTTTC | 25831 |
rs778331578 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164287 | TATGTTTACTTATCT[A/G]ATAAAACTTCAAAAA | 25831 |
rs778352345 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31105534 | TGTCTAGTACAACTG[A/G]CCTTGCTAAGAGGAT | 25831 |
rs778360812 | in-del | -/TGATAA | 1.72326e-05 | 0.0029353 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128044 | CAGTACAAATAGGTG[-/TGATAA]AGATTGTAGAAACCT | 25831 |
rs778364529 | snp | A/G/T | 4.97924e-05 | 0.0049894 | missense | HECTD1 | GRCh38.p7 | 14:31116236 | GTTAAAATTTCTTAC[A/G/T]TGTATGTGGGCTCCC | 25831 |
rs778379153 | snp | C/T | 1.65674e-05 | 0.00287809 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127956 | TCACTGTTGATGTAG[C/T]ACCAGGTGTGGTCAA | 25831 |
rs778384543 | snp | C/T | 1.65644e-05 | 0.00287783 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136657 | AAATCGTAATCTCCT[C/T]GTAAGTATCTACACA | 25831 |
rs778419129 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151727 | AAAATGTATAAACAT[G/T]TTGTAGCTCAGCCTG | 25831 |
rs778434317 | snp | A/G | 3.46903e-05 | 0.00416461 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133698 | TATGTTAGAGAAAAA[A/G]TTATGTAATATTTTA | 25831 |
rs778441593 | snp | A/C | 1.65963e-05 | 0.0028806 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148885 | AATAAACTTACATAT[A/C]TACATACTTACCCAG | 25831 |
rs778446852 | in-del | -/ATAAA/ATAAAATAAAATAAA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179429 | TCTCAAAATAAATAC[-/ATAAA/ATAAAATAAAATAAA]ATAAAATAAAATAAA | 25831 |
rs778447018 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31118766 | GGGCATGGTGGTGCA[C/T]GCCTGTAATCTCAGC | 25831 |
rs778470276 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136785 | ATAAACATAATAGAA[C/T]TATGAACAAATGTCT | 25831 |
rs778515679 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165731 | AGGCCCTATTCTGTA[A/T]CTCCTTGCCTTTGTA | 25831 |
rs778551693 | snp | A/C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31186787 | ATCCTAGCACTTTGG[A/C/G]AGGCTGAGGTGGGCA | 25831 |
rs778553439 | in-del | -/GTGTG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134558 | TGTGTGTGTGTGTGT[-/GTGTG]TGTGTGCGCGCGTAT | 25831 |
rs778555955 | snp | A/C/T | 3.3138e-05 | 0.00407039 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136669 | CCTTGTAAGTATCTA[A/C/T]ACAAAAACGATCAAA | 25831 |
rs778562805 | snp | C/G | 1.65767e-05 | 0.00287891 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31169463 | TGCACCATGCCGTAA[C/G]AGAGTCTAGAGAAGA | 25831 |
rs778635640 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198785 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCAGTA | 25831 |
rs778645580 | in-del | -/CCAATGTT | 1.65789e-05 | 0.0028791 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114263 | ATAGCCAAGAGTAAA[-/CCAATGTT]CCAATGTTCTAAAAT | 25831 |
rs778661586 | snp | A/G | 1.67576e-05 | 0.00289457 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112558 | CCTGCGAATTAACAA[A/G]TAATAATGTCTTAGT | 25831 |
rs778670980 | snp | A/T | 3.3168e-05 | 0.00407221 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175070 | GTCACGAATGAAGGT[A/T]AGCACACAATTCAAA | 25831 |
rs778691398 | snp | C/T | 1.69349e-05 | 0.00290984 | intron-variant | HECTD1 | GRCh38.p7 | 14:31174903 | GTATGTAACAGCAAC[C/T]TATTTACCTGATGAT | 25831 |
rs778704690 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31128532 | GATCTAGTTAAAAAC[C/T]GCAGCCAGAACAAGA | 25831 |
rs778706634 | snp | A/G | 1.67144e-05 | 0.00289084 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168481 | CAATCACCTACAGAC[A/G]AATATTTTTTAAAGA | 25831 |
rs778746541 | snp | A/G | | | | | GRCh38.p7 | 14:31177413 | TACTTGGGAGACTGA[A/G]GCAGGAGAACCGCTG | 25831 |
rs778755881 | snp | A/G | 1.67091e-05 | 0.00289038 | | | GRCh38.p7 | 14:31133487 | TTTAGTAAGTTAGAA[A/G]AGCCTCGTATCATCT | 25831 |
rs778784873 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144389 | TTCAAATTATTAACA[C/T]AAATTATGTCTACCA | 25831 |
rs778785832 | snp | G/T | 1.65641e-05 | 0.00287781 | synonymous-codon, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119764 | TAGTACGACCAGGTC[G/T]AGGATCAAAAGCAGG | 25831 |
rs778802763 | snp | C/G | 0.000125708 | 0.00792706 | missense | HECTD1 | GRCh38.p7 | 14:31113172 | GTGGAAAAGTAAACT[C/G]AAGCTGTTCATCACC | 25831 |
rs778826796 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31103215 | TGTGTAAAGAAAATG[C/T]GGTATATGTACACAA | 25831 |
rs778837343 | snp | A/C | 1.90221e-05 | 0.00308394 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135430 | CTAGAATTCTTTTAC[A/C]AAGTGAATATGGTCA | 25831 |
rs778861593 | in-del | -/CCCATTG | 1.67047e-05 | 0.00288999 | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100912 | AAGTCTCTGATGTCT[-/CCCATTG]CACTTCAAAGCTCAA | 25831 |
rs778880401 | in-del | -/ACACCCGC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104971 | GTGTGAGCCACCACC[-/ACACCCGC]ACACCCGACCACCAT | 25831 |
rs778883010 | snp | A/G | 1.65736e-05 | 0.00287863 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105542 | ACAACTGGCCTTGCT[A/G]AGAGGATATGTCAGA | 25831 |
rs779011847 | snp | A/G | 1.92927e-05 | 0.0031058 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156802 | TCAAAAAAAAAAAAA[A/G]AACTCTTCCTGATAC | 25831 |
rs779020118 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159805 | CCACCGTGCCCAGCT[A/G]ATTTTTCTATTTTTT | 25831 |
rs779029675 | snp | A/G | 1.65674e-05 | 0.00287809 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128702 | TCGTGGCATTAGTCC[A/G]TGCTATGTTTGCCAC | 25831 |
rs779069708 | snp | C/T | 1.84653e-05 | 0.00303848 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144972 | CAACAAATGTGAATT[C/T]TTACAATTAATAATT | 25831 |
rs779071139 | snp | C/G | 1.66147e-05 | 0.0028822 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31172084 | AGGCCCAGTTTAATA[C/G]AGTCTGACCTACATC | 25831 |
rs779078051 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31146055 | TTTTAGTTTGTGTTA[C/T]GAAATTTCAGTATCC | 25831 |
rs779085058 | snp | A/G | 1.66454e-05 | 0.00288486 | missense | HECTD1 | GRCh38.p7 | 14:31106928 | TCAAAGCTTCCTACC[A/G]AGAGTGAATCATGAC | 25831 |
rs779097321 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177901 | AGAATTTTTTTTTTT[-/A]GAAATTTTTTTTTTT | 25831 |
rs779118205 | in-del | -/ATTAGC | 1.65736e-05 | 0.00287863 | intron-variant | HECTD1 | GRCh38.p7 | 14:31105542 | CAACTGGCCTTGCTA[-/ATTAGC]AGAGGATATGTCAGA | 25831 |
rs779124645 | snp | A/G | 1.68004e-05 | 0.00289826 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31144898 | GGCATGCTTTCAACA[A/G]CTTTAAAATGGTCAT | 25831 |
rs779132022 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147354 | AAATAAAAAAGCTAT[A/G]TTCTTTCCAAAGTAT | 25831 |
rs779139180 | snp | A/C/G | 3.35285e-05 | 0.0040943 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113506 | AAACAATTAGAAAAA[A/C/G]TGGCCATTAATCACA | 25831 |
rs779146625 | snp | C/G | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178198 | AATACATTGTCTGGA[C/G]CACTTTCATCAAGAA | 25831 |
rs779157588 | snp | C/T | 1.656e-05 | 0.00287745 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135049 | ATGGCAAACCAGGCA[C/T]TCTTATCATCATTGC | 25831 |
rs779164734 | snp | A/G | 1.66713e-05 | 0.0028871 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173573 | TGAGAGCAGACTTAC[A/G]ATTGTTGACACCTGA | 25831 |
rs779189886 | snp | A/G | | | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168423 | TTCATCTTTGTTTGT[A/G]TCTTTCTTTTTCTTA | 25831 |
rs779193654 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182998 | ACAGCCACTGATTTA[C/T]GGCAAATACAGCCAA | 25831 |
rs779223663 | in-del | -/TTTA | 1.67111e-05 | 0.00289055 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172029 | ATTTAAATACCAGCT[-/TTTA]TTTATTAGCTTACCA | 25831 |
rs779236772 | snp | C/G | 1.66529e-05 | 0.00288551 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178020 | ATAAGTAATACTTAC[C/G]TTTACACACTGTTCG | 25831 |
rs779249784 | snp | C/T | 1.65641e-05 | 0.00287781 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157214 | AGTATTGTAGGCAAA[C/T]TGTGACCAACATCAG | 25831 |
rs779268669 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31145768 | CACCTACTCACTGAG[C/T]TGCTACTGATTTCAA | 25831 |
rs779287377 | in-del | -/TATC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151102 | TGTCTCTATTATCTA[-/TATC]TATCTATCTATCTAT | 25831 |
rs779289553 | in-del | -/AA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200491 | TCTCCATCTAATTTA[-/AA]AAAAAAAAAAAAAAA | 25831 |
rs779302950 | snp | C/G | 1.73691e-05 | 0.00294691 | intron-variant | HECTD1 | GRCh38.p7 | 14:31157040 | ATAAAAATAAGTTTA[C/G]TTGCCAGGAGTAGAG | 25831 |
rs779309289 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161427 | AAAAATAAAAATTAG[C/T]TGGACCTGGTGGTGT | 25831 |
rs779313604 | in-del | -/T | 4.9762e-05 | 0.00498784 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148830 | GAATATTCACAGAGC[-/T]TACTTTGTTACAATT | 25831 |
rs779346914 | snp | A/G | 1.67612e-05 | 0.00289488 | intron-variant | HECTD1 | GRCh38.p7 | 14:31121548 | ATGTCTAATTATTTG[A/G]CCCATATATGCCCCC | 25831 |
rs779382101 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125480 | GCCCGGCCAGTTCAC[C/T]CTTTCCTACCCACAA | 25831 |
rs779392930 | in-del | -/CCACTGCACT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115719 | TGAGCCATGATCGCA[-/CCACTGCACT]CCACTGCACTCCATC | 25831 |
rs779395532 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116212 | GGACATTATCTACCA[A/C]AACATTAAGTTAAAA | 25831 |
rs779400024 | snp | G/T | 1.65781e-05 | 0.00287902 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31121447 | TGCGAGGTAACAGCA[G/T]GATGCGTTACATCAG | 25831 |
rs779411085 | snp | A/G | 0.000182217 | 0.00954334 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31101233 | GTCCACCTGGGGGTA[A/G]AGTTGAACAACCAGT | 25831 |
rs779414861 | snp | C/G | 4.96824e-05 | 0.00498385 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129328 | ACAGTGGATGAAACA[C/G]GTTTGGGTGATGCCA | 25831 |
rs779458154 | snp | A/G | 1.69103e-05 | 0.00290773 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107738 | AATTGTGGGTTAAAC[A/G]TAAAGTTTGGGGTGT | 25831 |
rs779465778 | snp | C/T | 1.6638e-05 | 0.00288422 | intron-variant | HECTD1 | GRCh38.p7 | 14:31139856 | CTGTTCCTAGATGCA[C/T]TCAGCAATACTAGCT | 25831 |
rs779521911 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129307 | CATGATTGCGTTGTG[C/T]CTGAAACAGTGGATG | 25831 |
rs779532933 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198909 | AGTGTGGTTGTCTGC[A/G]CCTGTAGTCCCAGCT | 25831 |
rs779538675 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147743 | TTGGGCATCAAGAGC[A/G]AAACCGAGTCTCAAA | 25831 |
rs779551085 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139595 | ATAATTGTAGAATAA[A/G]AGGAACCCTTTTCTC | 25831 |
rs779568465 | snp | C/T | 3.31406e-05 | 0.00407053 | missense | HECTD1 | GRCh38.p7 | 14:31109527 | TCTCCAGGGTCATCT[C/T]GCCTAACACTGCTTG | 25831 |
rs779568622 | snp | C/T | 1.65605e-05 | 0.0028775 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129193 | CTGATGTCGCTGCTA[C/T]TGGCCACGCTACACA | 25831 |
rs779572492 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160454 | ACAGCCTAAACACTT[C/T]CATTAAGTATTGAAT | 25831 |
rs779572570 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31192590 | GGTTTATCACTAAAG[A/G]CCCTACAGATATCAA | 25831 |
rs779578748 | snp | G/T | 0.000210956 | 0.0102681 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149959 | AAAAAAACCAAACTG[G/T]AGAAACTAGGAAAAT | 25831 |
rs779587844 | in-del | -/TCACTTACTTGCTGTGCTCA | 1.70772e-05 | 0.00292204 | intron-variant | HECTD1 | GRCh38.p7 | 14:31128603 | TCCAGAAGGAAAAGC[-/TCACTTACTTGCTGTGCTCA]TCACTTACTTGCTGT | 25831 |
rs779599843 | snp | A/G | 5.17835e-05 | 0.00508813 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140032 | ATTAAGAGGTTTTGT[A/G]TAACTACATGTAAAT | 25831 |
rs779627495 | snp | C/T | 1.66275e-05 | 0.00288331 | intron-variant | HECTD1 | GRCh38.p7 | 14:31109349 | CACATTGGGCTGGTT[C/T]CCTAAGTGTCATTCC | 25831 |
rs779631192 | snp | C/T | 6.64949e-05 | 0.00576568 | missense | HECTD1 | GRCh38.p7 | 14:31106946 | AGTGAATCATGACCT[C/T]CTTCTGTAGAAGCTT | 25831 |
rs779631817 | in-del | -/TAGA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188094 | AGAGACAGCTGTAGA[-/TAGA]TAGATAGATAGATAG | 25831 |
rs779632050 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31117307 | GAACCTGGGAGTGGA[C/G]GTTGCAGTGAGCCGA | 25831 |
rs779652766 | snp | G/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153973 | TCAATTGGCCATATG[G/T]GTAGTGGGTCATTCA | 25831 |
rs779654434 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205626 | AGAGTTTCTTCACCT[A/G]CCAATTTTTATTTCT | 25831 |
rs779661149 | in-del | -/AGAC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188142 | GATAGATAGATAGAT[-/AGAC]AGACAGACAGATAAA | 25831 |
rs779742298 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177618 | GCTTAGAATAATGTC[-/T]TAGCACTGGTGGGTG | 25831 |
rs779753027 | snp | C/T | 1.65817e-05 | 0.00287933 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148919 | AGTTTCTGCAGTAAA[C/T]GAATGTTTGGTTCCT | 25831 |
rs779764080 | in-del | -/ATGTATATATATA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153734 | TATGGGACCCTAACC[-/ATGTATATATATA]ATGTATATATATAAT | 25831 |
rs779770102 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200068 | TCAATCTCTCAAACA[A/T]GGTCCTCTTTCCAGT | 25831 |
rs779773785 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189185 | CTAACCTACCATATG[C/T]CTAGTCACTCAAGTA | 25831 |
rs779779743 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31173013 | AAGCTGATAATTACA[A/T]AATTATGCACAGGGA | 25831 |
rs779787181 | snp | A/C | 1.72907e-05 | 0.00294025 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106600 | GAAACAAAAGCTTTA[A/C]AACTTATTCATGCAT | 25831 |
rs779819825 | snp | C/T | 1.65976e-05 | 0.00288072 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31175089 | ACACAATTCAAACCA[C/T]CAGCCTCAAAGACTG | 25831 |
rs779827286 | snp | A/G | 1.65809e-05 | 0.00287926 | missense | HECTD1 | GRCh38.p7 | 14:31116246 | CTTACGTGTATGTGG[A/G]CTCCCAAATACGCCT | 25831 |
rs779872603 | snp | A/G | 1.65712e-05 | 0.00287843 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127966 | TGTAGTACCAGGTGT[A/G]GTCAAATTAGGGAAA | 25831 |
rs779878183 | in-del | -/AA | 1.65741e-05 | 0.00287868 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136682 | TACACAAAAACGATC[-/AA]AATACTCTGGAAAAC | 25831 |
rs779879459 | snp | A/G | 3.32579e-05 | 0.00407773 | intron-variant | HECTD1 | GRCh38.p7 | 14:31169478 | CAGAGTCTAGAGAAG[A/G]AAAGCATTTAATTTG | 25831 |
rs779911615 | snp | C/T | 1.83135e-05 | 0.00302596 | missense | HECTD1 | GRCh38.p7 | 14:31113183 | AACTGAAGCTGTTCA[C/T]CACCATCTATAAAAT | 25831 |
rs779912767 | snp | C/T | | | intron-variant, downstream-variant-500B | HECTD1 | GRCh38.p7 | 14:31119669 | TCATATCTGATTTAG[C/T]ATGTATTAAAATTAA | 25831 |
rs779915358 | snp | G/T | 6.79163e-05 | 0.00582697 | intron-variant | HECTD1 | GRCh38.p7 | 14:31177998 | GAGAAAAATAAGTAA[G/T]GAGCCAATAAGTAAT | 25831 |
rs779921443 | snp | A/G | 1.65762e-05 | 0.00287886 | missense | HECTD1 | GRCh38.p7 | 14:31106737 | TCTCATCTTCAGAAA[A/G]ACCTTTGTTGCTTAA | 25831 |
rs779945022 | snp | G/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163530 | ATCCCTTGAGCCCAG[G/T]AGTTTGAAGTTGCCG | 25831 |
rs779951103 | in-del | -/AT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31130991 | ATTGGCCCAAAAAAC[-/AT]ACTCTCTCAACTCCT | 25831 |
rs779997449 | snp | A/G | 9.93706e-05 | 0.00704808 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173256 | ACTATCTAATCTCCG[A/G]AGTCCTGGGATTCTG | 25831 |
rs780011937 | snp | A/T | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31127815 | CTGCTTCCTGACCTG[A/T]GTCACTCTCACTGGA | 25831 |
rs780057021 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31170451 | TAAAAAGTCATCAAT[A/G]TATCCACCTCTATAC | 25831 |
rs780097211 | snp | A/G | 0.000243126 | 0.0110229 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133708 | AAAAAATTATGTAAT[A/G]TTTTAAAAGATGAAA | 25831 |
rs780107125 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31148681 | AAAATTTAACAAATC[A/G]GTATAAAAGACAAGA | 25831 |
rs780108739 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31102550 | TTCTCCTGTCTCAGC[C/T]TCCCAAGTAGCTGGG | 25831 |
rs780133895 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144685 | AATGGGGAGCAGGCC[A/G]GATTTGGCTCCTGGG | 25831 |
rs780150180 | snp | A/G | 1.66308e-05 | 0.00288359 | stop-gained, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133515 | TCTCTTTACCTAGCT[A/G]ATCTTCACATACTCC | 25831 |
rs780152350 | snp | A/G | 2.06405e-05 | 0.00321245 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144269 | TACACTAAAAGAAAA[A/G]AAAATTTAATGAAGG | 25831 |
rs780156206 | in-del | -/A | 0.00315222 | 0.0395749 | intron-variant | HECTD1 | GRCh38.p7 | 14:31172138 | CTGAAATTTTGAAGG[-/A]AAAAAAAAGAAACGT | 25831 |
rs780161561 | snp | A/C | 1.76465e-05 | 0.00297034 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116501 | CAATTATACTAAAAC[A/C]AGCAGTCCAAGAAAG | 25831 |
rs780170244 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203098 | CATATGAAAAAACAG[-/A]AAAGAAAAAAAGACT | 25831 |
rs780199974 | snp | C/T | 3.32458e-05 | 0.00407698 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31106948 | TGAATCATGACCTTC[C/T]TCTGTAGAAGCTTCA | 25831 |
rs780200526 | snp | A/G | 1.6628e-05 | 0.00288335 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173176 | GTGTCAATTGCATCT[A/G]TAAGTGCATCGGTAT | 25831 |
rs780201297 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195455 | ACCCATAAATAAAAA[C/T]GATAAAAATCTATCT | 25831 |
rs780207610 | snp | C/T | 1.6563e-05 | 0.00287771 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128936 | CAATTCCCATGGATA[C/T]TGCACTAGACTCCCC | 25831 |
rs780213142 | snp | C/T | 1.6569e-05 | 0.00287824 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31150213 | AGCATCTTCCTGTGG[C/T]TCATCTTCCTAAATG | 25831 |
rs780226394 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147629 | TGGGCATGGTGGCAG[C/G]CACCTGTAATCCCAG | 25831 |
rs780233296 | in-del | -/AA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31171452 | TTGATGAATACAAAC[-/AA]GAGAAAATATAGGCA | 25831 |
rs780265122 | snp | A/T | 4.98186e-05 | 0.00499067 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178237 | CAAAGGGCTGGTAAG[A/T]AAGTGCGAGGAGGAC | 25831 |
rs780266626 | snp | C/T | 1.87468e-05 | 0.00306154 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135446 | AAGTGAATATGGTCA[C/T]TCCAGCTTAAAGTAA | 25831 |
rs780273728 | snp | C/T | 1.65685e-05 | 0.00287819 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144989 | TACAATTAATAATTT[C/T]ACCAAATCTTCACTT | 25831 |
rs780305263 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134750 | AGTATCAAGTGATTT[A/G]TTTTTAGAAAGAAAA | 25831 |
rs780321277 | snp | A/C/G | 4.97354e-05 | 0.00498655 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148808 | TGAACCTTGGGGGGA[A/C/G]AAAAAAGAATATTCA | 25831 |
rs780328890 | snp | C/T | 3.31257e-05 | 0.00406962 | intron-variant | HECTD1 | GRCh38.p7 | 14:31168287 | ACACATCAAATAGTA[C/T]GAATAACTACCTTAT | 25831 |
rs780329290 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31169834 | ACAGTGAGCCAAGAT[C/T]GCTTGAACCATTGCA | 25831 |
rs780355550 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178895 | ATACTTAAGTGGTAC[-/T]TTTCATGTTCCTTAA | 25831 |
rs780360052 | snp | A/C | 1.66749e-05 | 0.00288741 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205766 | TGTCACTACAGTAAC[A/C]CAAAGGAACATGATG | 25831 |
rs780369667 | snp | C/T | 0.000397562 | 0.0140934 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149024 | AGCAATTTCTCCTTC[C/T]TTCAAACATGTCAGT | 25831 |
rs780380935 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | HECTD1 | GRCh38.p7 | 14:31208050 | TTGCTTGGCGCCGTG[A/G]CTAACACTTTGCGCG | 25831 |
rs780392515 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125904 | TATATGGTAAAGGGT[A/G]TTCCAAAACAATTGG | 25831 |
rs780400548 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31172807 | ATCTTTCAGGAATTA[-/T]TATTTGCTCATCACC | 25831 |
rs780422272 | in-del | -/GA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31137412 | TGGGATTACAGGCGT[-/GA]GACACCACGCCCAGC | 25831 |
rs780465559 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31126661 | AGATCTACTTCATGT[A/G]TAATCAGATAATTGC | 25831 |
rs780468993 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206428 | TTGAGGAAACTCTAA[A/G]CACCTTGATCCAATC | 25831 |
rs780469236 | in-del | -/TT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31203848 | GGTGTGCTGCACCCA[-/TT]TTAACTTGTCATTTA | 25831 |
rs780503949 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142545 | TCAAGCAATTCTCCC[A/G]CCTCAGAATTACAGA | 25831 |
rs780526540 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31115162 | TCAAATAAGGCAGTT[A/G]AGATCAATTTTTAAA | 25831 |
rs780534243 | snp | A/G | 1.6834e-05 | 0.00290116 | intron-variant | HECTD1 | GRCh38.p7 | 14:31103076 | ACCCATCTACATCGT[A/G]CATGTAACGGAAACA | 25831 |
rs780538862 | snp | A/G | 1.65647e-05 | 0.00287786 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31122995 | CTCAGGTAAGTCCTC[A/G]TCATCATCGAGCTCA | 25831 |
rs780541442 | snp | C/T | 4.96816e-05 | 0.00498381 | intron-variant | HECTD1 | GRCh38.p7 | 14:31122905 | AAGAGAATGGGGTAC[C/T]CTCTCTACCATAACC | 25831 |
rs780597045 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125514 | TCTTCAACTTCCCAT[A/G]ACCAAGAACTAATGC | 25831 |
rs780637888 | snp | C/T | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31157235 | CCAACATCAGAATCA[C/T]AAACTTCTTTTAACA | 25831 |
rs780641519 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31112397 | CTTATTCTAAAAACA[C/T]AAAAAAAAGGCTTCT | 25831 |
rs780657563 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189296 | TCGGTTTAGTATCTG[C/T]CCTTAGAATTCCAAC | 25831 |
rs780660891 | snp | A/G | 3.31658e-05 | 0.00407208 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31133325 | GGCCTCTGATAACAC[A/G]AGCTCCTGGAACCAT | 25831 |
rs780674282 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31142073 | TCACTACAATGTGAA[A/T]AAAATCATTCATCAT | 25831 |
rs780681872 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31174574 | AAAAATAAAAAATAC[C/T]GTCTTATTTAAATGA | 25831 |
rs780689596 | snp | A/C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31128160 | GGGAACCCAACTGAA[A/C/T]TCCAACTAAAAATTC | 25831 |
rs780702936 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156679 | TATGTTTAAAATTGT[A/T]GATCAAAATGTTTTA | 25831 |
rs780749251 | snp | A/G | 1.68943e-05 | 0.00290635 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173697 | GCAGCAGCCATTCGA[A/G]ATAACAGCTCCTCAG | 25831 |
rs780775490 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31201360 | TGCTCAATTTCCAGA[A/G]GACATAACTTTCAAA | 25831 |
rs780783696 | snp | C/T | 2.28898e-05 | 0.00338296 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31141902 | AGTTTTAAAAACATT[C/T]ATTCTTTCTACCAGT | 25831 |
rs780787427 | snp | A/G | 1.84865e-05 | 0.00304022 | intron-variant | HECTD1 | GRCh38.p7 | 14:31133192 | ATCTTAAAAGAAAAA[A/G]TTTAACTACCCATTT | 25831 |
rs780790730 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31169180 | ACAATCTCAAAGAAC[A/G]TAGAAAATTAAGCTG | 25831 |
rs780803289 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208169 | CAGCCACGATCTTCC[C/T]TCCTCGCGCACGGAA | 25831 |
rs780818201 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31139734 | ACTTCAAGTCATTAA[A/G]ATCAATCAAATGGCA | 25831 |
rs780826179 | snp | C/T | 1.65655e-05 | 0.00287793 | missense | HECTD1 | GRCh38.p7 | 14:31102947 | CCAGCTTAGGTTCAG[C/T]GTAATTGATAATATC | 25831 |
rs780828991 | in-del | -/TTTGT | 1.6646e-05 | 0.00288491 | frameshift-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31148728 | AGATATACCTTTTGC[-/TTTGT]TTTTTCTAACTTAGA | 25831 |
rs780863986 | snp | G/T | 1.70435e-05 | 0.00291915 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173709 | CGAGATAACAGCTCC[G/T]CAGTTAATCCATGCT | 25831 |
rs780886495 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202619 | CCTGCTGGGAGTTGA[C/T]TGTTTAAAAGAATTT | 25831 |
rs780886951 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31200356 | GGAAAAACCACTTCC[C/T]CTTTCTTGGCCAGGC | 25831 |
rs780896888 | snp | C/T | 3.35542e-05 | 0.00409585 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31149105 | TTGACTTGAAGTAGA[C/T]GGCTTTACTTGGCCT | 25831 |
rs780905397 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31189932 | CTTATGATTATAGTG[A/C]AAGTGACCACTGTGT | 25831 |
rs780918779 | in-del | -/TTCTTTCAC/TTCTTTCACATCGG/TTCTTTCACATCGGATTAAAATAAAAATGATTCTACTTA | 6.82112e-05 | 0.0058397 | intron-variant | HECTD1 | GRCh38.p7 | 14:31140016 | GAAGAAATAATTATT[lengthTooLong]ATTAAGAGGTTTTGT | 25831 |
rs780927406 | in-del | -/AATT | 4.68121e-05 | 0.00483775 | intron-variant | HECTD1 | GRCh38.p7 | 14:31113196 | CATCACCATCTATAA[-/AATT]AATTAATAAAATTAA | 25831 |
rs780952426 | snp | C/T | 3.31994e-05 | 0.00407414 | synonymous-codon | HECTD1 | GRCh38.p7 | 14:31109550 | ACTGCTTGTGGTTCT[C/T]GTTCGCTCCACAGTG | 25831 |
rs780953774 | snp | A/C | 1.6676e-05 | 0.00288751 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173603 | ATTACTCAATTTGGA[A/C]TCTGCAGTGGTGGAT | 25831 |
rs780976515 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131952 | AACCTGTTTTGATTA[A/C]AATGATTTGCAATTA | 25831 |
rs780999297 | snp | C/T | 4.96808e-05 | 0.00498377 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31135003 | ATGACGAAGTGTATA[C/T]GCTGATGGTATCACC | 25831 |
rs781021801 | snp | G/T | 1.66821e-05 | 0.00288804 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31171933 | ACCTCTATTAACATC[G/T]GCACCTCTCTCACAA | 25831 |
rs781025775 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31195446 | CAATGTCATACCCAT[-/A]AATAAAAATGATAAA | 25831 |
rs781038305 | snp | C/T | 1.71117e-05 | 0.00292499 | intron-variant | HECTD1 | GRCh38.p7 | 14:31149974 | TAGAAACTAGGAAAA[C/T]ATTTTAATTGAAACA | 25831 |
rs781045898 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31109732 | TTAAAACACAGTAAT[C/T]TTTTTTTGTTACATA | 25831 |
rs781047550 | snp | G/T | 1.68035e-05 | 0.00289853 | intron-variant | HECTD1 | GRCh38.p7 | 14:31116467 | GGGGTCCCTAAAAAT[G/T]TGGAAGATGGGTGAA | 25831 |
rs781060134 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31144563 | TGTGTGATTAAATTA[C/T]ATGGATACCGAAATC | 25831 |
rs781080921 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31124296 | TTTTTTCTCATCTTC[C/T]CTTTTTTACCAGCAT | 25831 |
rs781096138 | in-del | -/AATA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31132054 | CAAAGGGTTTATTTG[-/AATA]AATAAATGTCTTTAC | 25831 |
rs781127794 | snp | A/G | 1.65987e-05 | 0.00288082 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31156975 | TACTAAATCCCTTAT[A/G]ATCTGCAAAGCCAGC | 25831 |
rs781151761 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31108493 | AGTATAATAAAAACT[A/G]CAGCATATGGTTAAA | 25831 |
rs781153492 | snp | C/T | 3.31554e-05 | 0.00407144 | missense | HECTD1 | GRCh38.p7 | 14:31106745 | TCAGAAAGACCTTTG[C/T]TGCTTAAAATTTGGC | 25831 |
rs781156755 | snp | A/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31154013 | ACACTATTGTCACAC[A/T]TTCTTGATTACCAAA | 25831 |
rs781167036 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31191434 | AGGAGGCTGAGGCAG[A/G]GAAAAATGGCTTGAG | 25831 |
rs781173711 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31147082 | TTTGGGAGGCCGAGG[A/C]AGGTGGATCACTTGA | 25831 |
rs781212687 | in-del | -/A | 0.25728 | 0.249894 | intron-variant | HECTD1 | GRCh38.p7 | 14:31106167 | TTATCAGCAAACATT[-/A]AAAAAAAAAAGGCCT | 25831 |
rs781266263 | snp | A/G | 1.68278e-05 | 0.00290062 | intron-variant | HECTD1 | GRCh38.p7 | 14:31112574 | TAATAATGTCTTAGT[A/G]CTATAAGGCATTCAT | 25831 |
rs781268144 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152416 | GCTAGGCTCGAATTC[A/G]TGGGCTCAAGCGACC | 25831 |
rs781279794 | in-del | -/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110160 | GTGTGTGCCACCACG[-/C]CCAGCTAATTTTTGT | 25831 |
rs781283263 | snp | A/C | 1.67097e-05 | 0.00289043 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31128005 | ACCCATAAGAGGAGA[A/C]GCTAAAGACAAAAAT | 25831 |
rs781317618 | snp | A/G | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31178169 | AGTATGTTATGGCAC[A/G]GGCTGTCACCTCTAA | 25831 |
rs781338914 | snp | A/C/T | 3.31264e-05 | 0.00406968 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31119786 | AAAAGCAGGAACCAA[A/C/T]GCAGAAAACTGTCTC | 25831 |
rs781343408 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31135366 | ACCTACAAGTCAAAA[C/T]TCCTTAAACCACAGA | 25831 |
rs781379099 | in-del | -/TCA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31141384 | ATATTATCAAACATT[-/TCA]TCAGTGTTCAAATTT | 25831 |
rs781379576 | snp | C/T | 1.99455e-05 | 0.00315791 | intron-variant | HECTD1 | GRCh38.p7 | 14:31156807 | AAAAAAAAAAAAACT[C/T]TTCCTGATACCTCTA | 25831 |
rs781382427 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31104138 | GCATAGTAGGGTGAC[C/T]ATAGTTAACAATAAT | 25831 |
rs781393992 | snp | G/T | 1.65616e-05 | 0.00287759 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129038 | TGCTGGTGCTTGCAC[G/T]GGAAGATGACCCTAC | 25831 |
rs781417450 | snp | C/T | 2.67369e-05 | 0.00365619 | intron-variant | HECTD1 | GRCh38.p7 | 14:31144076 | AAATAATTTTTAAAA[C/T]TGTATTTTTGTTCTT | 25831 |
rs781425788 | in-del | -/A | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31207045 | AGGGAAGTTCTGGAG[-/A]AAGCAGCAGCAAGCC | 25831 |
rs781430645 | snp | A/G | 3.31219e-05 | 0.00406938 | missense, intron-variant, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31129160 | TCTGATCTCCGTTCC[A/G]TTTTGGTCGAACCCA | 25831 |
rs781438434 | in-del | -/ACA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31107946 | ATACATTTACTTCTC[-/ACA]ACAACCCTGCAAAAT | 25831 |
rs781439772 | snp | A/T | 1.80335e-05 | 0.00300273 | intron-variant | HECTD1 | GRCh38.p7 | 14:31114108 | CAATTATAAAGTCTA[A/T]GATATTTCACATGCA | 25831 |
rs781460723 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31204588 | AATGAAATCTATGAA[C/T]GCAATTTTTAACTTG | 25831 |
rs781461347 | snp | A/C/G | 6.62881e-05 | 0.00575676 | intron-variant | HECTD1 | GRCh38.p7 | 14:31136678 | TATCTACACAAAAAC[A/C/G]ATCAAAATACTCTGG | 25831 |
rs781476665 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110955 | AAACTTTTTAAATGC[-/T]TTTTTTTTTTTGGTA | 25831 |
rs781483780 | snp | A/G/T | 3.31237e-05 | 0.00406952 | synonymous-codon, missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31136641 | GTGCACGTTCCAACC[A/G/T]AAATCGTAATCTCCT | 25831 |
rs781509286 | snp | C/T | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31209266 | ATATGTTCCTAGACA[C/T]AGGAAAGGTCACCTG | 25831 |
rs781511995 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31158553 | GCGTGAGCCACCACG[A/C]CCGGCCAAATTAACC | 25831 |
rs781518500 | snp | C/T | 1.65619e-05 | 0.00287762 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31173273 | GTCCTGGGATTCTGC[C/T]TGTAGATCCAGCACT | 25831 |
rs781524914 | snp | A/C | 3.32254e-05 | 0.00407573 | utr-variant-5-prime, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31205947 | GCCATGGTTTTTTAA[A/C]AGTCTCTTTGCTTAA | 25831 |
rs781545472 | snp | C/T | 1.6593e-05 | 0.00288031 | intron-variant | HECTD1 | GRCh38.p7 | 14:31205790 | CATGATGAAGGAATG[C/T]ACTTACGTTTCAAAA | 25831 |
rs781556696 | snp | C/T | 3.31296e-05 | 0.00406985 | missense | HECTD1 | GRCh38.p7 | 14:31101058 | GATAGCTTGCATCAG[C/T]AGCATCAACCTACAA | 25831 |
rs781611264 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31116203 | TCTACACTAGGACAT[C/T]ATCTACCAAAACATT | 25831 |
rs781613939 | snp | A/C | 8.6423e-05 | 0.00657298 | intron-variant | HECTD1 | GRCh38.p7 | 14:31107288 | AATGCAAATAAAATT[A/C]AACAAAAGTTAATAG | 25831 |
rs781631989 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31151680 | CAGGCATGAGCCACC[A/G]CGCCTGACTCAGCAT | 25831 |
rs781634753 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198141 | CTAGATGAAGCAAAA[C/T]TATTAAATTTACTAA | 25831 |
rs781634825 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31167848 | GTTGTTAAATTATCT[A/G]TATTCCCAGAGAACC | 25831 |
rs781647835 | snp | A/G | 1.81319e-05 | 0.00301091 | intron-variant | HECTD1 | GRCh38.p7 | 14:31135465 | AGCTTAAAGTAAAAT[A/G]ACTGACTTACTTTGC | 25831 |
rs781713220 | snp | A/G | 9.97622e-05 | 0.00706195 | missense | HECTD1 | GRCh38.p7 | 14:31107147 | AAATGAAACAGTTTC[A/G]TGATCCTTTCAAGCT | 25831 |
rs781720580 | snp | C/T | | | utr-variant-3-prime | HECTD1 | GRCh38.p7 | 14:31100833 | AAAAAAGGCAAGTGT[C/T]ATTAGCATGGTGGAT | 25831 |
rs781733191 | snp | A/C | 7.06564e-05 | 0.00594333 | intron-variant | HECTD1 | GRCh38.p7 | 14:31148678 | CTGAAAATTTAACAA[A/C]TCAGTATAAAAGACA | 25831 |
rs781753179 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31164582 | TTAAGTATAACTATC[C/T]TCACCTTGGAGACGA | 25831 |
rs781754903 | snp | A/G | 3.31323e-05 | 0.00407002 | synonymous-codon, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31123015 | CATCGAGCTCAGCCA[A/G]TAGAGTACTGGCACG | 25831 |
rs781770147 | snp | C/G | 1.65712e-05 | 0.00287843 | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168455 | CATCTCCTTTATTAA[C/G]TGGACACATCCAATC | 25831 |
rs796094755 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31205670 | ACACAAAACTCTTCA[A/G]GAATATTTTTAAAGA | 25831 |
rs796106282 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31169951 | TGTACTTGGTTATTT[A/G]TCATCATCTCAAATT | 25831 |
rs796112750 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31183936 | TAGTCTTGAACTCCT[A/G]GGCTCCAGCAATCTT | 25831 |
rs796192559 | snp | A/C | | | missense, nc-transcript-variant | HECTD1 | GRCh38.p7 | 14:31168359 | GCAATAACCTTTTCA[A/C]GTATATGGGTGCCAT | 25831 |
rs796195768 | in-del | -/AC | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31179594 | AGTCTAATGCTTATT[-/AC]ACAAACCTGTCCAAG | 25831 |
rs796256981 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177879 | TAAAGTAAGACTGAA[A/G]ATAGGAAGAATTTTT | 25831 |
rs796271708 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31178644 | TCATCTGTACTAAAA[A/G]TGCAAAAAATCAGCC | 25831 |
rs796272622 | in-del | -/TG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31122390 | CGCATGTGTGTGTGT[-/TG]GTGTGTGTGTCATTC | 25831 |
rs796293865 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187992 | AACTCCAGACCTCAG[A/G]TGATCTGCCCACCTT | 25831 |
rs796325393 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136435 | GGCCAAACTGTATTA[C/T]CATAACTCTGGATAT | 25831 |
rs796342329 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31125624 | GCAATGAATTTATAA[C/T]ACTTTGGTGTAATCA | 25831 |
rs796357066 | in-del | AAAGAAAAAAAAGA/GG | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31161589 | AAAAAGAAAAAAAAA[AAAGAAAAAAAAGA/GG]AGAAAGAAAGGAAAA | 25831 |
rs796369750 | in-del | -/AA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31156549 | CACACACACACACAC[-/AA]ACAGATACATGTGTC | 25831 |
rs796428947 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31175303 | TGTGGTAGCTCACAC[C/T]TGTGATCCCAGCACT | 25831 |
rs796494514 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131528 | TACTTCAATAAAATG[C/T]TTATGTATGTATAGG | 25831 |
rs796503301 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31172570 | CACTGCACTCCAGCC[C/T]GCACAACAGAGCGAG | 25831 |
rs796520814 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31155095 | TCACGCCTGTAATAC[C/T]GACAGTTTGGGAGGC | 25831 |
rs796528276 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196837 | GATACTGTATCTGCT[-/A]AAAAAAAAAAACAAA | 25831 |
rs796534490 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31169058 | AAAAAAAAAAAAAAA[-/T]TTTTTTTTGGTCAAA | 25831 |
rs796585537 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31177900 | AAGAATTTTTTTTTT[-/T]AGAAATTTTTTTTTT | 25831 |
rs796607561 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165854 | TCAGAGAGTGAAACC[-/T]TTTTTTTTTTAGATG | 25831 |
rs796619566 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31188781 | TTTCTGCATCCAGAA[C/T]GAGAAGCCAAATGAA | 25831 |
rs796632530 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31187929 | AATTTTATTTTTGTA[-/T]TTTTTTAGTAGAGAC | 25831 |
rs796632658 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31133799 | ACTTTCATATTAACT[A/C]AACAGTTCATTACAA | 25831 |
rs796633551 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31159696 | CCCAGGCTGGAGTGC[A/G]TGGCAGGATTTTGAC | 25831 |
rs796664020 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31140620 | TCATCTATAACCTAT[A/C]ACACAGTATTACCAC | 25831 |
rs796671387 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31196758 | ACTCCGTCTCAAAAC[-/A]AAAAAAAAAAAAAAG | 25831 |
rs796736012 | snp | C/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31136904 | TCGGTTCACTGCAAG[C/T]TTCACCTCCCGGGTT | 25831 |
rs796744202 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31182838 | CCTGGGCAATAGAGT[A/G]AGACTCTGTCTCAGA | 25831 |
rs796751716 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31163272 | TACAAAAAAAAAAAA[-/A]CTATTTTAATTAGCC | 25831 |
rs796766696 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31131029 | CCCAAAAGATAAACC[-/A]AAAAAAAAAAAAAAT | 25831 |
rs796781309 | in-del | -/A | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31185356 | CAAAACAAAAAACAG[-/A]AAAAAAAAAAAACCT | 25831 |
rs796796432 | in-del | -/CTAAAACA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31140708 | ATAGTTTGCAAAGAG[-/CTAAAACA]CTAAAACACAGTAAT | 25831 |
rs796797946 | in-del | -/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31110007 | TTAAAACAATTTTTC[-/T]TTTTTTTTTTTTGAG | 25831 |
rs796820024 | snp | C/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31153664 | TTTTCCTCTAGAAGT[C/G]TCATAATTTTAGTGT | 25831 |
rs796843359 | snp | A/G | | | upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31208124 | GCCCAACCTGTCCCC[A/G]CTGAGCCTTCCGCCC | 25831 |
rs796858177 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31198657 | TTTGCAAAAGTAAAC[A/G]TGGGTAAAACAGTCA | 25831 |
rs796872567 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31165146 | TGCTTGTATTTTAAT[A/G]TCAGCTCATAATACT | 25831 |
rs796877102 | snp | A/C | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31152608 | GTGGCTCACACCTGT[A/C]ATCTCAGCACTTTGG | 25831 |
rs796895747 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31157599 | GAATGTTAACATGTC[A/G]TGATAATTTTAGAAA | 25831 |
rs796911457 | in-del | -/CA | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31202199 | AGCGAGACTCTGCCT[-/CA]AAAAAAAAAAAAAAA | 25831 |
rs796913345 | snp | A/G | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31119081 | GGCTCACTGCTCGTC[A/G]TCACTCTGACTCCTG | 25831 |
rs796955408 | in-del | CGC/T | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31134569 | TGTGTGTGTGTGTGC[CGC/T]CGTATGTATATACAG | 25831 |
rs796987200 | in-del | -/GTT | | | intron-variant | HECTD1 | GRCh38.p7 | 14:31160514 | ACTGATTCAAAAAAG[-/GTT]GTTAACACCTTAAAT | 25831 |
rs797008435 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | HECTD1 | GRCh38.p7 | 14:31206627 | TTAAAAGTTAAAAAA[-/AT]AAAAAAATTAAAAAA | 25831 |